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Compile Data Set for Download or QSAR

Found 102 hits with Last Name = 'huang' and Initial = 'ls'   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50603567
PNG
(CHEMBL5172755)
Show SMILES NC(=N)NCCC[C@H](NCc1ccccn1)C(=O)NCc1ccc(CNCCCNC2CCCCC2)cc1 |r|
PDB

UniProtKB/SwissProt

antibodypedia
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MCE
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 1.60n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114150
BindingDB Entry DOI: 10.7270/Q26W9G5W
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50035696
PNG
(1,1''-{1,4-phenylenebis(methylene)}-bis{1,4,8,11-t...)
Show SMILES C(N1CCCNCCNCCCNCC1)c1ccc(CN2CCCNCCNCCCNCC2)cc1
Show InChI InChI=1S/C28H54N8/c1-9-29-15-17-31-13-3-21-35(23-19-33-11-1)25-27-5-7-28(8-6-27)26-36-22-4-14-32-18-16-30-10-2-12-34-20-24-36/h5-8,29-34H,1-4,9-26H2
PDB

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antibodypedia
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CHEMBL
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Patents


Similars

n/an/a 2.90n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50035696
PNG
(1,1''-{1,4-phenylenebis(methylene)}-bis{1,4,8,11-t...)
Show SMILES C(N1CCCNCCNCCCNCC1)c1ccc(CN2CCCNCCNCCCNCC2)cc1
Show InChI InChI=1S/C28H54N8/c1-9-29-15-17-31-13-3-21-35(23-19-33-11-1)25-27-5-7-28(8-6-27)26-36-22-4-14-32-18-16-30-10-2-12-34-20-24-36/h5-8,29-34H,1-4,9-26H2
PDB

UniProtKB/SwissProt

antibodypedia
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MCE
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Similars

Article
PubMed
n/an/a 3.10n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114150
BindingDB Entry DOI: 10.7270/Q26W9G5W
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50603567
PNG
(CHEMBL5172755)
Show SMILES NC(=N)NCCC[C@H](NCc1ccccn1)C(=O)NCc1ccc(CNCCCNC2CCCCC2)cc1 |r|
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
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MCE
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 12n/an/an/an/an/an/a


TBA



Citation and Details

Article DOI: 10.1016/j.ejmech.2022.114150
BindingDB Entry DOI: 10.7270/Q26W9G5W
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50524293
PNG
(CHEMBL4542285)
Show SMILES CC(C)C[C@@H](N)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@H](CO)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)NCCCCCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CS)C(O)=O |r|
Show InChI InChI=1S/C122H206N46O33S/c1-62(2)49-69(127)98(180)146-58-93(176)148-63(3)97(179)163-85(59-169)111(193)157-79(50-66-56-145-70-26-9-8-25-68(66)70)106(188)158-80(51-67-57-139-61-147-67)107(189)156-78(34-22-46-144-122(137)138)116(198)167-47-23-36-88(167)113(195)160-83(55-94(177)178)110(192)154-74(29-12-16-40-125)102(184)151-73(28-11-15-39-124)101(183)150-71(31-19-43-141-119(131)132)99(181)140-42-18-6-7-37-92(175)149-72(27-10-14-38-123)100(182)153-76(32-20-44-142-120(133)134)103(185)152-75(30-13-17-41-126)104(186)165-95(64(4)170)114(196)161-82(53-90(129)173)108(190)159-81(52-89(128)172)109(191)162-84(54-91(130)174)117(199)168-48-24-35-87(168)112(194)155-77(33-21-45-143-121(135)136)105(187)166-96(65(5)171)115(197)164-86(60-202)118(200)201/h8-9,25-26,56-57,61-65,69,71-88,95-96,145,169-171,202H,6-7,10-24,27-55,58-60,123-127H2,1-5H3,(H2,128,172)(H2,129,173)(H2,130,174)(H,139,147)(H,140,181)(H,146,180)(H,148,176)(H,149,175)(H,150,183)(H,151,184)(H,152,185)(H,153,182)(H,154,192)(H,155,194)(H,156,189)(H,157,193)(H,158,188)(H,159,190)(H,160,195)(H,161,196)(H,162,191)(H,163,179)(H,164,197)(H,165,186)(H,166,187)(H,177,178)(H,200,201)(H4,131,132,141)(H4,133,134,142)(H4,135,136,143)(H4,137,138,144)/t63-,64-,65-,69-,71-,72+,73-,74-,75+,76+,77+,78-,79-,80-,81+,82+,83-,84+,85-,86+,87+,88-,95+,96+/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
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KEGG
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 14n/an/an/an/an/an/a



University of California San Diego

Curated by ChEMBL


Assay Description
Competitive binding affinity to CXCR4 in human SupT1 cells incubated for 40 mins by 12G5 antibody based fluorescence analysis


Eur J Med Chem 172: 174-185 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.056
BindingDB Entry DOI: 10.7270/Q2MS3X5P
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50524293
PNG
(CHEMBL4542285)
Show SMILES CC(C)C[C@@H](N)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@H](CO)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)NCCCCCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CS)C(O)=O |r|
Show InChI InChI=1S/C122H206N46O33S/c1-62(2)49-69(127)98(180)146-58-93(176)148-63(3)97(179)163-85(59-169)111(193)157-79(50-66-56-145-70-26-9-8-25-68(66)70)106(188)158-80(51-67-57-139-61-147-67)107(189)156-78(34-22-46-144-122(137)138)116(198)167-47-23-36-88(167)113(195)160-83(55-94(177)178)110(192)154-74(29-12-16-40-125)102(184)151-73(28-11-15-39-124)101(183)150-71(31-19-43-141-119(131)132)99(181)140-42-18-6-7-37-92(175)149-72(27-10-14-38-123)100(182)153-76(32-20-44-142-120(133)134)103(185)152-75(30-13-17-41-126)104(186)165-95(64(4)170)114(196)161-82(53-90(129)173)108(190)159-81(52-89(128)172)109(191)162-84(54-91(130)174)117(199)168-48-24-35-87(168)112(194)155-77(33-21-45-143-121(135)136)105(187)166-96(65(5)171)115(197)164-86(60-202)118(200)201/h8-9,25-26,56-57,61-65,69,71-88,95-96,145,169-171,202H,6-7,10-24,27-55,58-60,123-127H2,1-5H3,(H2,128,172)(H2,129,173)(H2,130,174)(H,139,147)(H,140,181)(H,146,180)(H,148,176)(H,149,175)(H,150,183)(H,151,184)(H,152,185)(H,153,182)(H,154,192)(H,155,194)(H,156,189)(H,157,193)(H,158,188)(H,159,190)(H,160,195)(H,161,196)(H,162,191)(H,163,179)(H,164,197)(H,165,186)(H,166,187)(H,177,178)(H,200,201)(H4,131,132,141)(H4,133,134,142)(H4,135,136,143)(H4,137,138,144)/t63-,64-,65-,69-,71-,72+,73-,74-,75+,76+,77+,78-,79-,80-,81+,82+,83-,84+,85-,86+,87+,88-,95+,96+/m1/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 16n/an/an/an/an/an/a



University of California San Diego

Curated by ChEMBL


Assay Description
Competitive binding affinity to CXCR4 receptor (unknown origin) expressed in CHO cells incubated for 40 mins by 12G5 antibody based fluorescence anal...


Eur J Med Chem 172: 174-185 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.056
BindingDB Entry DOI: 10.7270/Q2MS3X5P
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50524292
PNG
(CHEMBL4521504)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCCN)NC(=O)CCCCCNC(=O)[C@@H](CCCNC(N)=N)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CC(O)=O)NC(=O)[C@H]1CCCN1C(=O)[C@@H](CCCNC(N)=N)NC(=O)[C@@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](CO)NC(=O)[C@@H](C)NC(=O)CNC(=O)[C@H](N)CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CS)C(N)=O |r|
Show InChI InChI=1S/C123H207N47O30S/c1-7-66(4)98(118(199)161-81(34-23-47-144-122(135)136)110(191)160-82(38-39-92(129)172)105(186)152-68(6)101(182)163-85(52-70-57-139-63-149-70)113(194)168-90(62-201)99(130)180)169-115(196)87(54-96(176)177)154-95(175)60-148-104(185)75(28-12-16-40-124)155-109(190)80(33-22-46-143-121(133)134)158-106(187)77(29-13-17-41-125)153-93(173)37-9-8-20-44-141-103(184)76(32-21-45-142-120(131)132)156-107(188)78(30-14-18-42-126)157-108(189)79(31-15-19-43-127)159-114(195)88(55-97(178)179)166-117(198)91-36-25-49-170(91)119(200)83(35-24-48-145-123(137)138)162-112(193)86(53-71-58-140-64-150-71)165-111(192)84(51-69-56-146-74-27-11-10-26-72(69)74)164-116(197)89(61-171)167-100(181)67(5)151-94(174)59-147-102(183)73(128)50-65(2)3/h10-11,26-27,56-58,63-68,73,75-91,98,146,171,201H,7-9,12-25,28-55,59-62,124-128H2,1-6H3,(H2,129,172)(H2,130,180)(H,139,149)(H,140,150)(H,141,184)(H,147,183)(H,148,185)(H,151,174)(H,152,186)(H,153,173)(H,154,175)(H,155,190)(H,156,188)(H,157,189)(H,158,187)(H,159,195)(H,160,191)(H,161,199)(H,162,193)(H,163,182)(H,164,197)(H,165,192)(H,166,198)(H,167,181)(H,168,194)(H,169,196)(H,176,177)(H,178,179)(H4,131,132,142)(H4,133,134,143)(H4,135,136,144)(H4,137,138,145)/t66-,67+,68-,73+,75-,76+,77-,78+,79+,80-,81-,82-,83+,84+,85-,86+,87-,88+,89+,90-,91+,98-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 18n/an/an/an/an/an/a



University of California San Diego

Curated by ChEMBL


Assay Description
Competitive binding affinity to CXCR4 receptor (unknown origin) expressed in CHO cells incubated for 40 mins by 12G5 antibody based fluorescence anal...


Eur J Med Chem 172: 174-185 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.056
BindingDB Entry DOI: 10.7270/Q2MS3X5P
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421849
PNG
(CHEMBL5283078)
Show SMILES CCOC(=O)C1CNc2c(OC)cc(Cc3cnc(N)nc3N)c(OC)c2C1
Show InChI InChI=1S/C19H25N5O4/c1-4-28-18(25)12-6-13-15(22-9-12)14(26-2)7-10(16(13)27-3)5-11-8-23-19(21)24-17(11)20/h7-8,12,22H,4-6,9H2,1-3H3,(H4,20,21,23,24)
PDB

UniProtKB/SwissProt

antibodypedia
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CHEMBL
PC cid
PC sid
UniChem

Similars

n/an/a 20n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563581
PNG
(CHEMBL4797911)
Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc1cccc(c1)C(C)=O |r|
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 22n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50524292
PNG
(CHEMBL4521504)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@H](CCCCN)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CCCCN)NC(=O)CCCCCNC(=O)[C@@H](CCCNC(N)=N)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CCCCN)NC(=O)[C@@H](CC(O)=O)NC(=O)[C@H]1CCCN1C(=O)[C@@H](CCCNC(N)=N)NC(=O)[C@@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](CO)NC(=O)[C@@H](C)NC(=O)CNC(=O)[C@H](N)CC(C)C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1cnc[nH]1)C(=O)N[C@@H](CS)C(N)=O |r|
Show InChI InChI=1S/C123H207N47O30S/c1-7-66(4)98(118(199)161-81(34-23-47-144-122(135)136)110(191)160-82(38-39-92(129)172)105(186)152-68(6)101(182)163-85(52-70-57-139-63-149-70)113(194)168-90(62-201)99(130)180)169-115(196)87(54-96(176)177)154-95(175)60-148-104(185)75(28-12-16-40-124)155-109(190)80(33-22-46-143-121(133)134)158-106(187)77(29-13-17-41-125)153-93(173)37-9-8-20-44-141-103(184)76(32-21-45-142-120(131)132)156-107(188)78(30-14-18-42-126)157-108(189)79(31-15-19-43-127)159-114(195)88(55-97(178)179)166-117(198)91-36-25-49-170(91)119(200)83(35-24-48-145-123(137)138)162-112(193)86(53-71-58-140-64-150-71)165-111(192)84(51-69-56-146-74-27-11-10-26-72(69)74)164-116(197)89(61-171)167-100(181)67(5)151-94(174)59-147-102(183)73(128)50-65(2)3/h10-11,26-27,56-58,63-68,73,75-91,98,146,171,201H,7-9,12-25,28-55,59-62,124-128H2,1-6H3,(H2,129,172)(H2,130,180)(H,139,149)(H,140,150)(H,141,184)(H,147,183)(H,148,185)(H,151,174)(H,152,186)(H,153,173)(H,154,175)(H,155,190)(H,156,188)(H,157,189)(H,158,187)(H,159,195)(H,160,191)(H,161,199)(H,162,193)(H,163,182)(H,164,197)(H,165,192)(H,166,198)(H,167,181)(H,168,194)(H,169,196)(H,176,177)(H,178,179)(H4,131,132,142)(H4,133,134,143)(H4,135,136,144)(H4,137,138,145)/t66-,67+,68-,73+,75-,76+,77-,78+,79+,80-,81-,82-,83+,84+,85-,86+,87-,88+,89+,90-,91+,98-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
KEGG
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 23n/an/an/an/an/an/a



University of California San Diego

Curated by ChEMBL


Assay Description
Competitive binding affinity to CXCR4 in human SupT1 cells incubated for 40 mins by 12G5 antibody based fluorescence analysis


Eur J Med Chem 172: 174-185 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.056
BindingDB Entry DOI: 10.7270/Q2MS3X5P
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50612662
PNG
(CHEMBL5280362)
Show SMILES CC(C)C[C@@H](N)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@H](CO)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)N(CCCCCC(O)=O)[C@@H](CCCCN[C@H](CS)C(=O)N[C@@H]([C@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@H](C)O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(N)=O)C(N)=O |r|
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
n/an/a 25n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563589
PNG
(CHEMBL4744255)
Show SMILES COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)c2ccc(o2)-c2ccc(cc2)C(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc2cccc(c2)C(C)=O)cc1 |r|
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
Article
PubMed
n/an/a 25n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563587
PNG
(CHEMBL4765143)
Show SMILES COc1cc(NC(=O)C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)OCc2ccccc2)cc(OC)c1 |r|
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TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50612663
PNG
(CHEMBL5280204)
Show SMILES CC(C)C[C@@H](N)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@H](CO)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)N(CCCCCC(O)=O)[C@H](CCCCN[C@@H](CS)C(=O)N[C@H]([C@@H](C)O)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(N)=O)C(=O)N[C@H](CC(N)=O)C(=O)N[C@H](CC(N)=O)C(=O)N[C@H]([C@@H](C)O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(N)=O)C(N)=O |r|
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TBA



Citation and Details
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563590
PNG
(CHEMBL4753369)
Show SMILES COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)c2ccc(o2)-c2ccc(cc2)C(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc2cccc(OC)c2)cc1 |r|
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TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563578
PNG
(CHEMBL4743601)
Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc1cccc(c1)C(C)=O |r|
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TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563588
PNG
(CHEMBL4790349)
Show SMILES COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)c2ccc(o2)-c2ccc(cc2)C(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc2cc(OC)cc(OC)c2)cc1 |r|
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TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563586
PNG
(CHEMBL4745732)
Show SMILES CCc1cccc(NC(=O)C(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)OCc2ccccc2)c1 |r|
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TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563569
PNG
(CHEMBL4793363)
Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc1ccccc1 |r|
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TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421854
PNG
(CHEMBL5269411)
Show SMILES CC1CCNc2ccc(Cc3cnc(N)nc3N)cc12
Show InChI InChI=1S/C15H19N5/c1-9-4-5-18-13-3-2-10(7-12(9)13)6-11-8-19-15(17)20-14(11)16/h2-3,7-9,18H,4-6H2,1H3,(H4,16,17,19,20)
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TBA



Citation and Details
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563585
PNG
(CHEMBL4760977)
Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc1cccc2CCCc12 |r|
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TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50612661
PNG
(CHEMBL5290756)
Show SMILES CC(C)C[C@@H](N)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@H](CO)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)N(CCCCCC(O)=O)[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)N[C@H](CCCCN)C(=O)N[C@@H](CS)C(=O)N[C@H]([C@@H](C)O)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(N)=O)C(=O)N[C@H](CC(N)=O)C(=O)N[C@H](CC(N)=O)C(=O)N[C@H]([C@@H](C)O)C(N)=O |r|
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TBA



Citation and Details
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50612658
PNG
(CHEMBL5273020)
Show SMILES CC(C)C[C@@H](N)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@H](CO)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)N(CCCCCC(O)=O)[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H](CCCNC(N)=N)C(=O)NCC(=O)N1CCC[C@@H]1C(=O)NCC(=O)N[C@H](CCCNC(N)=N)C(=O)N[C@H](C)C(=O)N[C@H](Cc1ccccc1)C(N)=O |r|
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TBA



Citation and Details
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50035696
PNG
(1,1''-{1,4-phenylenebis(methylene)}-bis{1,4,8,11-t...)
Show SMILES C(N1CCCNCCNCCCNCC1)c1ccc(CN2CCCNCCNCCCNCC2)cc1
Show InChI InChI=1S/C28H54N8/c1-9-29-15-17-31-13-3-21-35(23-19-33-11-1)25-27-5-7-28(8-6-27)26-36-22-4-14-32-18-16-30-10-2-12-34-20-24-36/h5-8,29-34H,1-4,9-26H2
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n/an/a 44n/an/an/an/an/an/a



University of California San Diego

Curated by ChEMBL


Assay Description
Competitive binding affinity to CXCR4 in human SupT1 cells incubated for 40 mins by 12G5 antibody based fluorescence analysis


Eur J Med Chem 172: 174-185 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.056
BindingDB Entry DOI: 10.7270/Q2MS3X5P
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50612660
PNG
(CHEMBL5267316)
Show SMILES CC(C)C[C@@H](N)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@H](CO)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)N(CCCCCC(O)=O)[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CS)C(=O)N[C@@H]([C@H](C)O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H]([C@H](C)O)C(N)=O |r|
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TBA



Citation and Details
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421857
PNG
(CHEMBL5290852)
Show SMILES COCCOc1cc(Cc2cnc(N)nc2N)cc2cccnc12
Show InChI InChI=1S/C17H19N5O2/c1-23-5-6-24-14-9-11(7-12-3-2-4-20-15(12)14)8-13-10-21-17(19)22-16(13)18/h2-4,7,9-10H,5-6,8H2,1H3,(H4,18,19,21,22)
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TBA



Citation and Details
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50035696
PNG
(1,1''-{1,4-phenylenebis(methylene)}-bis{1,4,8,11-t...)
Show SMILES C(N1CCCNCCNCCCNCC1)c1ccc(CN2CCCNCCNCCCNCC2)cc1
Show InChI InChI=1S/C28H54N8/c1-9-29-15-17-31-13-3-21-35(23-19-33-11-1)25-27-5-7-28(8-6-27)26-36-22-4-14-32-18-16-30-10-2-12-34-20-24-36/h5-8,29-34H,1-4,9-26H2
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n/an/a 51n/an/an/an/an/an/a



University of California San Diego

Curated by ChEMBL


Assay Description
Competitive binding affinity to CXCR4 receptor (unknown origin) expressed in CHO cells incubated for 40 mins by 12G5 antibody based fluorescence anal...


Eur J Med Chem 172: 174-185 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.056
BindingDB Entry DOI: 10.7270/Q2MS3X5P
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563568
PNG
(CHEMBL4743123)
Show SMILES COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)c2ccc(o2)-c2ccc(cc2)C(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc2ccccc2)cc1 |r|
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TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50007203
PNG
(CHEMBL3237875)
Show SMILES COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)CN2CCOCC2)C(=O)N[C@@H](Cc2ccccc2)C(=O)[C@@]2(C)CO2)cc1 |r|
Show InChI InChI=1S/C31H40N4O7/c1-21(32-27(36)19-35-13-15-41-16-14-35)29(38)34-26(18-23-9-11-24(40-3)12-10-23)30(39)33-25(28(37)31(2)20-42-31)17-22-7-5-4-6-8-22/h4-12,21,25-26H,13-20H2,1-3H3,(H,32,36)(H,33,39)(H,34,38)/t21-,25-,26-,31+/m0/s1
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TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563579
PNG
(CHEMBL4799577)
Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc1cccc(c1)S(C)(=O)=O |r|
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Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563577
PNG
(CHEMBL4749833)
Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc1cccc(c1)C(C)=O |r|
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Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563583
PNG
(CHEMBL4792535)
Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc1cccc2cnccc12 |r|
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Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563572
PNG
(CHEMBL4794207)
Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc1ccccc1 |r|
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Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421853
PNG
(CHEMBL5282178)
Show SMILES Cc1ccnc2c(N)cc(Cc3cnc(N)nc3N)cc12
Show InChI InChI=1S/C15H16N6/c1-8-2-3-19-13-11(8)5-9(6-12(13)16)4-10-7-20-15(18)21-14(10)17/h2-3,5-7H,4,16H2,1H3,(H4,17,18,20,21)
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n/an/a 68n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421860
PNG
(CHEMBL5283630)
Show SMILES COc1cc(Cc2cnc(N)nc2N)cc2C(C)CCN(CCOC(C)=O)c12
Show InChI InChI=1S/C20H27N5O3/c1-12-4-5-25(6-7-28-13(2)26)18-16(12)9-14(10-17(18)27-3)8-15-11-23-20(22)24-19(15)21/h9-12H,4-8H2,1-3H3,(H4,21,22,23,24)
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n/an/a 68n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421856
PNG
(CHEMBL5277914)
Show SMILES Cc1ccnc2ccc(Cc3cnc(N)nc3N)cc12
Show InChI InChI=1S/C15H15N5/c1-9-4-5-18-13-3-2-10(7-12(9)13)6-11-8-19-15(17)20-14(11)16/h2-5,7-8H,6H2,1H3,(H4,16,17,19,20)
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n/an/a 69n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421859
PNG
(CHEMBL5285076)
Show SMILES CC1CC(C)c2cc(Cc3cnc(N)nc3N)cc(Cl)c2N1
Show InChI InChI=1S/C16H20ClN5/c1-8-3-9(2)21-14-12(8)5-10(6-13(14)17)4-11-7-20-16(19)22-15(11)18/h5-9,21H,3-4H2,1-2H3,(H4,18,19,20,22)
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n/an/a 81n/an/an/an/an/an/a


TBA



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More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563582
PNG
(CHEMBL4746065)
Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc1cccc2ncccc12 |r|
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n/an/a 100n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50612657
PNG
(CHEMBL5281510)
Show SMILES CC(C)C[C@@H](N)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@H](CO)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)N(CCCCCC(O)=O)[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N1CCC[C@H]1C(=O)NCC(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1ccccc1)C(N)=O |r|
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TBA



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More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421861
PNG
(CHEMBL5275975)
Show SMILES Nc1ncc(Cc2ccc3ncccc3c2)c(N)n1
Show InChI InChI=1S/C14H13N5/c15-13-11(8-18-14(16)19-13)7-9-3-4-12-10(6-9)2-1-5-17-12/h1-6,8H,7H2,(H4,15,16,18,19)
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n/an/a 119n/an/an/an/an/an/a


TBA



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More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421849
PNG
(CHEMBL5283078)
Show SMILES CCOC(=O)C1CNc2c(OC)cc(Cc3cnc(N)nc3N)c(OC)c2C1
Show InChI InChI=1S/C19H25N5O4/c1-4-28-18(25)12-6-13-15(22-9-12)14(26-2)7-10(16(13)27-3)5-11-8-23-19(21)24-17(11)20/h7-8,12,22H,4-6,9H2,1-3H3,(H4,20,21,23,24)
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n/an/a 119n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421863
PNG
(CHEMBL5277386)
Show SMILES COc1cc(Cc2cnc(N)nc2N)cc2c(C)cc(C)nc12
Show InChI InChI=1S/C17H19N5O/c1-9-4-10(2)21-15-13(9)6-11(7-14(15)23-3)5-12-8-20-17(19)22-16(12)18/h4,6-8H,5H2,1-3H3,(H4,18,19,20,22)
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n/an/a 122n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Proteasome subunit beta type-2


(Homo sapiens (Human))
BDBM50563589
PNG
(CHEMBL4744255)
Show SMILES COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)c2ccc(o2)-c2ccc(cc2)C(C)=O)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc2cccc(c2)C(C)=O)cc1 |r|
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n/an/a 133n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of 20S immunoproteasome beta 2 trypsin-like activity in human H226 cell using Z-LRR-aminoluciferin as substrate for 10 mins by fluorescenc...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563567
PNG
(CHEMBL4748545)
Show SMILES COc1ccc(C[C@H](NC(=O)[C@H](C)NC(=O)c2ccc(cc2)-c2ccccc2)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc2ccccc2)cc1 |r|
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n/an/a 134n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50524291
PNG
(CHEMBL4469971)
Show SMILES CC(C)C[C@@H](N)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@H](CO)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CS)C(=O)N[C@H](CS)C(=O)N[C@H](CC(C)C)C(=O)NCC(=O)N[C@H](Cc1ccc(O)cc1)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(C)C)C(=O)N1CCC[C@@H]1C(=O)NCCCCCC(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C151H249N45O36S2/c1-81(2)60-93(156)127(210)168-72-120(202)173-87(13)126(209)190-111(76-197)141(224)186-107(67-89-70-167-94-33-17-16-32-92(89)94)137(220)187-108(68-90-71-163-80-172-90)138(221)183-101(39-28-56-166-151(161)162)148(231)195-58-30-41-116(195)145(228)188-109(69-124(206)207)139(222)180-98(37-21-25-53-155)132(215)192-114(79-234)143(226)193-113(78-233)142(225)185-103(62-83(5)6)130(213)171-75-123(205)177-106(66-88-44-46-91(199)47-45-88)136(219)181-99(48-49-118(157)200)133(216)179-97(36-20-24-52-154)131(214)182-100(38-27-55-165-150(159)160)147(230)196-59-31-42-117(196)146(229)189-110(65-86(11)12)149(232)194-57-29-40-115(194)144(227)164-54-26-14-15-43-119(201)174-96(35-19-23-51-153)128(211)169-73-121(203)175-104(63-84(7)8)134(217)184-102(61-82(3)4)129(212)170-74-122(204)176-105(64-85(9)10)135(218)191-112(77-198)140(223)178-95(125(158)208)34-18-22-50-152/h16-17,32-33,44-47,70-71,80-87,93,95-117,167,197-199,233-234H,14-15,18-31,34-43,48-69,72-79,152-156H2,1-13H3,(H2,157,200)(H2,158,208)(H,163,172)(H,164,227)(H,168,210)(H,169,211)(H,170,212)(H,171,213)(H,173,202)(H,174,201)(H,175,203)(H,176,204)(H,177,205)(H,178,223)(H,179,216)(H,180,222)(H,181,219)(H,182,214)(H,183,221)(H,184,217)(H,185,225)(H,186,224)(H,187,220)(H,188,228)(H,189,229)(H,190,209)(H,191,218)(H,192,215)(H,193,226)(H,206,207)(H4,159,160,165)(H4,161,162,166)/t87-,93-,95+,96+,97-,98-,99-,100-,101-,102+,103-,104+,105+,106-,107-,108-,109-,110-,111-,112+,113-,114-,115-,116-,117-/m1/s1
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n/an/a 147n/an/an/an/an/an/a



University of California San Diego

Curated by ChEMBL


Assay Description
Competitive binding affinity to CXCR4 receptor (unknown origin) expressed in CHO cells incubated for 40 mins by 12G5 antibody based fluorescence anal...


Eur J Med Chem 172: 174-185 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.056
BindingDB Entry DOI: 10.7270/Q2MS3X5P
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421858
PNG
(CHEMBL5276826)
Show SMILES CCN1CCC(C)c2cc(Cc3cnc(N)nc3N)ccc12
Show InChI InChI=1S/C17H23N5/c1-3-22-7-6-11(2)14-9-12(4-5-15(14)22)8-13-10-20-17(19)21-16(13)18/h4-5,9-11H,3,6-8H2,1-2H3,(H4,18,19,20,21)
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n/an/a 147n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50524291
PNG
(CHEMBL4469971)
Show SMILES CC(C)C[C@@H](N)C(=O)NCC(=O)N[C@H](C)C(=O)N[C@H](CO)C(=O)N[C@H](Cc1c[nH]c2ccccc12)C(=O)N[C@H](Cc1cnc[nH]1)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(O)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CS)C(=O)N[C@H](CS)C(=O)N[C@H](CC(C)C)C(=O)NCC(=O)N[C@H](Cc1ccc(O)cc1)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H](CCCCN)C(=O)N[C@H](CCCNC(N)=N)C(=O)N1CCC[C@@H]1C(=O)N[C@H](CC(C)C)C(=O)N1CCC[C@@H]1C(=O)NCCCCCC(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C151H249N45O36S2/c1-81(2)60-93(156)127(210)168-72-120(202)173-87(13)126(209)190-111(76-197)141(224)186-107(67-89-70-167-94-33-17-16-32-92(89)94)137(220)187-108(68-90-71-163-80-172-90)138(221)183-101(39-28-56-166-151(161)162)148(231)195-58-30-41-116(195)145(228)188-109(69-124(206)207)139(222)180-98(37-21-25-53-155)132(215)192-114(79-234)143(226)193-113(78-233)142(225)185-103(62-83(5)6)130(213)171-75-123(205)177-106(66-88-44-46-91(199)47-45-88)136(219)181-99(48-49-118(157)200)133(216)179-97(36-20-24-52-154)131(214)182-100(38-27-55-165-150(159)160)147(230)196-59-31-42-117(196)146(229)189-110(65-86(11)12)149(232)194-57-29-40-115(194)144(227)164-54-26-14-15-43-119(201)174-96(35-19-23-51-153)128(211)169-73-121(203)175-104(63-84(7)8)134(217)184-102(61-82(3)4)129(212)170-74-122(204)176-105(64-85(9)10)135(218)191-112(77-198)140(223)178-95(125(158)208)34-18-22-50-152/h16-17,32-33,44-47,70-71,80-87,93,95-117,167,197-199,233-234H,14-15,18-31,34-43,48-69,72-79,152-156H2,1-13H3,(H2,157,200)(H2,158,208)(H,163,172)(H,164,227)(H,168,210)(H,169,211)(H,170,212)(H,171,213)(H,173,202)(H,174,201)(H,175,203)(H,176,204)(H,177,205)(H,178,223)(H,179,216)(H,180,222)(H,181,219)(H,182,214)(H,183,221)(H,184,217)(H,185,225)(H,186,224)(H,187,220)(H,188,228)(H,189,229)(H,190,209)(H,191,218)(H,192,215)(H,193,226)(H,206,207)(H4,159,160,165)(H4,161,162,166)/t87-,93-,95+,96+,97-,98-,99-,100-,101-,102+,103-,104+,105+,106-,107-,108-,109-,110-,111-,112+,113-,114-,115-,116-,117-/m1/s1
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n/an/a 147n/an/an/an/an/an/a



University of California San Diego

Curated by ChEMBL


Assay Description
Competitive binding affinity to CXCR4 in human SupT1 cells incubated for 40 mins by 12G5 antibody based fluorescence analysis


Eur J Med Chem 172: 174-185 (2019)


Article DOI: 10.1016/j.ejmech.2019.03.056
BindingDB Entry DOI: 10.7270/Q2MS3X5P
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50421852
PNG
(CHEMBL5283007)
Show SMILES COc1cc(Cc2cnc(N)nc2N)cc2CC(COC(C)=O)CNc12
Show InChI InChI=1S/C18H23N5O3/c1-10(24)26-9-12-5-13-3-11(6-15(25-2)16(13)21-7-12)4-14-8-22-18(20)23-17(14)19/h3,6,8,12,21H,4-5,7,9H2,1-2H3,(H4,19,20,22,23)
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n/an/a 156n/an/an/an/an/an/a


TBA



Citation and Details
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563570
PNG
(CHEMBL4798244)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](C)NC(=O)OCc1ccccc1)C(=O)C(=O)Nc1ccccc1 |r|
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n/an/a 156n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
Proteasome subunit beta type-8


(Homo sapiens (Human))
BDBM50563580
PNG
(CHEMBL4743273)
Show SMILES CC(C)C[C@H](NC(=O)OCc1ccccc1)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)C(=O)Nc1cccc2ccccc12 |r|
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n/an/a 165n/an/an/an/an/an/a


TBA

Assay Description
Inhibition of 20S immunoproteasome beta 5 chymotrypsin-like activity in human H226 cell using Suc-LLVY-AMC as substrate for 10 mins by fluorescence b...


Citation and Details

Article DOI: 10.1016/j.ejmech.2021.113267
BindingDB Entry DOI: 10.7270/Q2FN19XD
More data for this
Ligand-Target Pair
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