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SMILES: CCC(C)[C@H](NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)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](CCSC)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CS)C(N)=O

InChI Key: InChIKey=FNPWTVDCPMRARS-VMRMJYOXSA-N

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 1 hit for monomerid = 81824   
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
Pituitary adenylate cyclase-activating polypeptide


(RAT)
BDBM81824
PNG
(PACAP(1-33,Cys34))
Show SMILES CCC(C)[C@H](NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](N)Cc1cnc[nH]1)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)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](CCSC)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CC(C)C)C(=O)NCC(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CS)C(N)=O |r|
Show InChI InChI=1S/C179H285N53O48S2/c1-16-95(10)143(229-138(244)85-200-151(255)129(81-139(245)246)221-171(275)131(86-233)225-149(253)110(185)80-105-83-195-90-201-105)175(279)223-128(75-100-33-18-17-19-34-100)169(273)232-144(99(14)236)176(280)224-130(82-140(247)248)168(272)227-133(88-235)172(276)220-127(79-104-49-57-109(240)58-50-104)167(271)226-132(87-234)170(274)211-118(42-32-71-198-179(193)194)160(264)218-125(77-102-45-53-107(238)54-46-102)165(269)210-116(40-30-69-196-177(189)190)157(261)206-112(36-21-26-65-181)154(258)212-119(59-61-135(186)241)161(265)214-121(63-72-282-15)152(256)203-98(13)148(252)230-141(93(6)7)173(277)215-115(39-24-29-68-184)156(260)207-114(38-23-28-67-183)158(262)219-126(78-103-47-55-108(239)56-48-103)166(270)216-123(74-92(4)5)163(267)204-96(11)146(250)202-97(12)147(251)231-142(94(8)9)174(278)222-122(73-91(2)3)150(254)199-84-137(243)205-111(35-20-25-64-180)153(257)208-117(41-31-70-197-178(191)192)159(263)217-124(76-101-43-51-106(237)52-44-101)164(268)209-113(37-22-27-66-182)155(259)213-120(60-62-136(187)242)162(266)228-134(89-281)145(188)249/h17-19,33-34,43-58,83,90-99,110-134,141-144,233-240,281H,16,20-32,35-42,59-82,84-89,180-185H2,1-15H3,(H2,186,241)(H2,187,242)(H2,188,249)(H,195,201)(H,199,254)(H,200,255)(H,202,250)(H,203,256)(H,204,267)(H,205,243)(H,206,261)(H,207,260)(H,208,257)(H,209,268)(H,210,269)(H,211,274)(H,212,258)(H,213,259)(H,214,265)(H,215,277)(H,216,270)(H,217,263)(H,218,264)(H,219,262)(H,220,276)(H,221,275)(H,222,278)(H,223,279)(H,224,280)(H,225,253)(H,226,271)(H,227,272)(H,228,266)(H,229,244)(H,230,252)(H,231,251)(H,232,273)(H,245,246)(H,247,248)(H4,189,190,196)(H4,191,192,197)(H4,193,194,198)/t95?,96-,97-,98-,99+,110-,111-,112-,113-,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129-,130-,131-,132-,133-,134-,141-,142-,143-,144-/m0/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
6.40n/an/an/an/an/an/an/an/a



Georg-August-University

Curated by PDSP Ki Database




Eur J Biochem 202: 951-8 (1991)


Article DOI: 10.1111/j.1432-1033.1991.tb16455.x
BindingDB Entry DOI: 10.7270/Q2PR7TG8
More data for this
Ligand-Target Pair