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Compile Data Set for Download or QSAR

Marvin 2D Structure

The following exact ligands are found in BindingDB

Wt: 3138.7
BDBM50196243

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB (change energy unit to kcal/mol)

Found 2 hits in this display   
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))
BDBM50196243
PNG
(CHEMBL3923006)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(cc1)C(=O)c1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)NCCOCCOCCOCCC(=O)NCCCC[C@H](NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](N)CCCNC(N)=N)C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1)C(O)=O |r|
Show InChI InChI=1S/C147H221N41O32S2/c1-86(2)75-108(177-134(208)114(82-189)184-132(206)112(78-87-38-48-94(49-39-87)121(195)93-24-4-3-5-25-93)182-138(212)118-36-21-67-187(118)140(214)100(152)27-8-12-57-148)129(203)183-115(83-190)135(209)178-109(77-88-41-50-96(191)51-42-88)123(197)164-66-70-219-72-74-220-73-71-218-69-56-120(194)163-60-15-11-31-107(142(216)217)176-136(210)116-84-221-222-85-117(186-133(207)113(81-91-40-47-92-23-6-7-26-95(92)76-91)179-127(201)102(32-17-62-166-144(155)156)170-122(196)99(151)28-16-61-165-143(153)154)137(211)180-110(79-89-43-52-97(192)53-44-89)130(204)173-103(33-18-63-167-145(157)158)124(198)171-101(29-9-13-58-149)126(200)175-106(30-10-14-59-150)141(215)188-68-22-37-119(188)139(213)181-111(80-90-45-54-98(193)55-46-90)131(205)174-104(34-19-64-168-146(159)160)125(199)172-105(128(202)185-116)35-20-65-169-147(161)162/h3-7,23-26,38-55,76,86,99-119,189-193H,8-22,27-37,56-75,77-85,148-152H2,1-2H3,(H,163,194)(H,164,197)(H,170,196)(H,171,198)(H,172,199)(H,173,204)(H,174,205)(H,175,200)(H,176,210)(H,177,208)(H,178,209)(H,179,201)(H,180,211)(H,181,213)(H,182,212)(H,183,203)(H,184,206)(H,185,202)(H,186,207)(H,216,217)(H4,153,154,165)(H4,155,156,166)(H4,157,158,167)(H4,159,160,168)(H4,161,162,169)/t99-,100-,101-,102-,103-,104-,105-,106+,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 112n/an/an/an/an/an/a



Universit£ de Sherbrooke

Curated by ChEMBL


Assay Description
Displacement of [125I]-CXCL12 from HA-tagged human recombinant CXCR4 expressed in HEK293 cells incubated for 1 hr by gamma-radiation counting analysi...


J Med Chem 59: 7512-24 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00566
BindingDB Entry DOI: 10.7270/Q2MP5576
More data for this
Ligand-Target Pair
C-X-C chemokine receptor type 4


(Homo sapiens (Human))
BDBM50196243
PNG
(CHEMBL3923006)
Show SMILES CC(C)C[C@H](NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(cc1)C(=O)c1ccccc1)NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)NCCOCCOCCOCCC(=O)NCCCC[C@H](NC(=O)[C@@H]1CSSC[C@H](NC(=O)[C@H](Cc2ccc3ccccc3c2)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H](N)CCCNC(N)=N)C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@H](CCCCN)C(=O)N2CCC[C@H]2C(=O)N[C@@H](Cc2ccc(O)cc2)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1)C(O)=O |r|
Show InChI InChI=1S/C147H221N41O32S2/c1-86(2)75-108(177-134(208)114(82-189)184-132(206)112(78-87-38-48-94(49-39-87)121(195)93-24-4-3-5-25-93)182-138(212)118-36-21-67-187(118)140(214)100(152)27-8-12-57-148)129(203)183-115(83-190)135(209)178-109(77-88-41-50-96(191)51-42-88)123(197)164-66-70-219-72-74-220-73-71-218-69-56-120(194)163-60-15-11-31-107(142(216)217)176-136(210)116-84-221-222-85-117(186-133(207)113(81-91-40-47-92-23-6-7-26-95(92)76-91)179-127(201)102(32-17-62-166-144(155)156)170-122(196)99(151)28-16-61-165-143(153)154)137(211)180-110(79-89-43-52-97(192)53-44-89)130(204)173-103(33-18-63-167-145(157)158)124(198)171-101(29-9-13-58-149)126(200)175-106(30-10-14-59-150)141(215)188-68-22-37-119(188)139(213)181-111(80-90-45-54-98(193)55-46-90)131(205)174-104(34-19-64-168-146(159)160)125(199)172-105(128(202)185-116)35-20-65-169-147(161)162/h3-7,23-26,38-55,76,86,99-119,189-193H,8-22,27-37,56-75,77-85,148-152H2,1-2H3,(H,163,194)(H,164,197)(H,170,196)(H,171,198)(H,172,199)(H,173,204)(H,174,205)(H,175,200)(H,176,210)(H,177,208)(H,178,209)(H,179,201)(H,180,211)(H,181,213)(H,182,212)(H,183,203)(H,184,206)(H,185,202)(H,186,207)(H,216,217)(H4,153,154,165)(H4,155,156,166)(H4,157,158,167)(H4,159,160,168)(H4,161,162,169)/t99-,100-,101-,102-,103-,104-,105-,106+,107-,108-,109-,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/an/an/a 207n/an/an/an/a



Universit£ de Sherbrooke

Curated by ChEMBL


Assay Description
Agonist activity at HA-tagged human CXCR4 receptor expressed in HEK293 cells co-transfected with Galphai1-91-RlucII, Gbeta1, and GFP10-G-gamma1 incub...


J Med Chem 59: 7512-24 (2016)


Article DOI: 10.1021/acs.jmedchem.6b00566
BindingDB Entry DOI: 10.7270/Q2MP5576
More data for this
Ligand-Target Pair