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BDBM50153495 CHEMBL3774594

SMILES: CCCCC(NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc1cccc2ccccc12)C(=O)N[C@@H](CCC(O)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(N)=O

InChI Key: InChIKey=FHOSQSIFQMKBAO-POKSWYTKSA-N

Data: 2 KI

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50153495   
Target/Host
(Institution)		LigandTarget/Host
Links		Ligand
Links		Trg + Lig
Links		Ki
nM		ΔG°
kcal/mole		IC50
nM		Kd
nM		EC50/IC50
nM		koff
s-1		kon
M-1s-1		pHTemp
°C
Corticotropin releasing factor receptor 1


(Homo sapiens (Human))		BDBM50153495
PNG
(CHEMBL3774594)
Show SMILES CCCCC(NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc1cccc2ccccc12)C(=O)N[C@@H](CCC(O)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(N)=O |r|
Show InChI InChI=1S/C186H298N52O49/c1-28-30-50-113(214-163(269)122(60-67-142(247)248)221-166(272)129(78-95(9)10)232-178(284)146(99(17)18)234-164(270)123(61-68-143(249)250)220-158(264)118(55-43-74-203-184(196)197)217-165(271)126(75-92(3)4)226-167(273)128(77-94(7)8)227-172(278)134(83-111-89-199-91-205-111)230-169(275)131(80-107-44-32-31-33-45-107)233-179(285)148(105(24)239)235-175(281)130(79-96(11)12)228-174(280)136(85-145(253)254)210-106(25)240)154(260)206-101(20)150(256)211-116(53-41-72-201-182(192)193)155(261)207-102(21)151(257)213-121(59-66-141(245)246)162(268)222-124(57-64-138(189)242)176(282)237-185(26,86-97(13)14)180(286)209-104(23)153(259)212-119(56-63-137(188)241)161(267)219-120-58-65-140(244)200-71-39-37-52-115(216-171(277)133(82-110-88-198-90-204-110)224-152(258)103(22)208-156(120)262)160(266)231-135(84-139(190)243)173(279)218-117(54-42-73-202-183(194)195)157(263)215-114(51-36-38-70-187)159(265)225-127(76-93(5)6)168(274)229-132(81-109-48-40-47-108-46-34-35-49-112(108)109)170(276)223-125(62-69-144(251)252)177(283)238-186(27,87-98(15)16)181(287)236-147(149(191)255)100(19)29-2/h31-35,40,44-49,88-105,113-136,146-148,239H,28-30,36-39,41-43,50-87,187H2,1-27H3,(H2,188,241)(H2,189,242)(H2,190,243)(H2,191,255)(H,198,204)(H,199,205)(H,200,244)(H,206,260)(H,207,261)(H,208,262)(H,209,286)(H,210,240)(H,211,256)(H,212,259)(H,213,257)(H,214,269)(H,215,263)(H,216,277)(H,217,271)(H,218,279)(H,219,267)(H,220,264)(H,221,272)(H,222,268)(H,223,276)(H,224,258)(H,225,265)(H,226,273)(H,227,278)(H,228,280)(H,229,274)(H,230,275)(H,231,266)(H,232,284)(H,233,285)(H,234,270)(H,235,281)(H,236,287)(H,237,282)(H,238,283)(H,245,246)(H,247,248)(H,249,250)(H,251,252)(H,253,254)(H4,192,193,201)(H4,194,195,202)(H4,196,197,203)/t100-,101-,102-,103-,104-,105+,113?,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129-,130-,131+,132?,133-,134-,135-,136-,146-,147-,148-,185?,186?/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
PubMed
 0.5n/an/an/an/an/an/an/an/a



Salk Institute

Curated by ChEMBL


Assay Description
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in human CRF-R1 expressed in COS-M6 cells after 90 mins by gamma counting assay

J Med Chem 59: 854-66 (2016)


BindingDB Entry DOI: 10.7270/Q2WQ05NH
More data for this
Ligand-Target Pair
Corticotropin releasing factor receptor 2


(Mus musculus)		BDBM50153495
PNG
(CHEMBL3774594)
Show SMILES CCCCC(NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(O)=O)NC(C)=O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CCC(N)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@H]1CCC(=O)NCCCC[C@H](NC(=O)[C@H](Cc2cnc[nH]2)NC(=O)[C@H](C)NC1=O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)NC(Cc1cccc2ccccc12)C(=O)N[C@@H](CCC(O)=O)C(=O)NC(C)(CC(C)C)C(=O)N[C@@H]([C@@H](C)CC)C(N)=O |r|
Show InChI InChI=1S/C186H298N52O49/c1-28-30-50-113(214-163(269)122(60-67-142(247)248)221-166(272)129(78-95(9)10)232-178(284)146(99(17)18)234-164(270)123(61-68-143(249)250)220-158(264)118(55-43-74-203-184(196)197)217-165(271)126(75-92(3)4)226-167(273)128(77-94(7)8)227-172(278)134(83-111-89-199-91-205-111)230-169(275)131(80-107-44-32-31-33-45-107)233-179(285)148(105(24)239)235-175(281)130(79-96(11)12)228-174(280)136(85-145(253)254)210-106(25)240)154(260)206-101(20)150(256)211-116(53-41-72-201-182(192)193)155(261)207-102(21)151(257)213-121(59-66-141(245)246)162(268)222-124(57-64-138(189)242)176(282)237-185(26,86-97(13)14)180(286)209-104(23)153(259)212-119(56-63-137(188)241)161(267)219-120-58-65-140(244)200-71-39-37-52-115(216-171(277)133(82-110-88-198-90-204-110)224-152(258)103(22)208-156(120)262)160(266)231-135(84-139(190)243)173(279)218-117(54-42-73-202-183(194)195)157(263)215-114(51-36-38-70-187)159(265)225-127(76-93(5)6)168(274)229-132(81-109-48-40-47-108-46-34-35-49-112(108)109)170(276)223-125(62-69-144(251)252)177(283)238-186(27,87-98(15)16)181(287)236-147(149(191)255)100(19)29-2/h31-35,40,44-49,88-105,113-136,146-148,239H,28-30,36-39,41-43,50-87,187H2,1-27H3,(H2,188,241)(H2,189,242)(H2,190,243)(H2,191,255)(H,198,204)(H,199,205)(H,200,244)(H,206,260)(H,207,261)(H,208,262)(H,209,286)(H,210,240)(H,211,256)(H,212,259)(H,213,257)(H,214,269)(H,215,263)(H,216,277)(H,217,271)(H,218,279)(H,219,267)(H,220,264)(H,221,272)(H,222,268)(H,223,276)(H,224,258)(H,225,265)(H,226,273)(H,227,278)(H,228,280)(H,229,274)(H,230,275)(H,231,266)(H,232,284)(H,233,285)(H,234,270)(H,235,281)(H,236,287)(H,237,282)(H,238,283)(H,245,246)(H,247,248)(H,249,250)(H,251,252)(H,253,254)(H4,192,193,201)(H4,194,195,202)(H4,196,197,203)/t100-,101-,102-,103-,104-,105+,113?,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129-,130-,131+,132?,133-,134-,135-,136-,146-,147-,148-,185?,186?/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars
PubMed
 4n/an/an/an/an/an/an/an/a



Salk Institute

Curated by ChEMBL


Assay Description
Displacement of [125ITyr0-Glu1,Nle17]-PS-Svg in mouse CRF-R2 beta expressed in COS-M6 cells after 90 mins by gamma counting assay

J Med Chem 59: 854-66 (2016)


BindingDB Entry DOI: 10.7270/Q2WQ05NH
More data for this
Ligand-Target Pair