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Compile Data Set for Download or QSAR

Found 2 hits Enz. Inhib. hit(s) with Target = 'Pituitary adenylate cyclase-activating polypeptide type I receptor' and Ligand = 'BDBM50250075'   
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
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50250075
PNG
(CHEMBL526315 | [Bip6]PACAP38)
Show SMILES CC[C@H](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](Cc1ccc(cc1)-c1ccccc1)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](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C209H335N63O53S/c1-18-113(12)168(268-162(285)103-236-176(296)153(99-163(286)287)261-199(319)155(104-273)265-174(294)130(217)97-125-101-230-107-237-125)204(324)263-151(92-118-53-63-124(64-54-118)123-40-20-19-21-41-123)197(317)272-169(117(16)276)205(325)264-154(100-164(288)289)196(316)267-157(106-275)200(320)259-150(96-122-61-71-129(280)72-62-122)194(314)266-156(105-274)198(318)249-140(51-38-87-233-208(226)227)186(306)257-148(94-120-57-67-127(278)68-58-120)192(312)248-138(49-36-85-231-206(222)223)182(302)243-133(44-24-31-80-212)179(299)251-143(74-76-159(219)282)188(308)252-144(77-89-326-17)177(297)239-116(15)173(293)269-165(110(6)7)201(321)253-136(47-27-34-83-215)181(301)244-135(46-26-33-82-214)183(303)258-149(95-121-59-69-128(279)70-60-121)193(313)255-146(91-109(4)5)190(310)240-114(13)171(291)238-115(14)172(292)270-166(111(8)9)203(323)262-145(90-108(2)3)175(295)235-102-161(284)241-132(43-23-30-79-211)178(298)245-139(50-37-86-232-207(224)225)185(305)256-147(93-119-55-65-126(277)66-56-119)191(311)247-134(45-25-32-81-213)180(300)250-142(73-75-158(218)281)187(307)246-141(52-39-88-234-209(228)229)189(309)271-167(112(10)11)202(322)254-137(48-28-35-84-216)184(304)260-152(98-160(220)283)195(315)242-131(170(221)290)42-22-29-78-210/h19-21,40-41,53-72,101,107-117,130-157,165-169,273-280H,18,22-39,42-52,73-100,102-106,210-217H2,1-17H3,(H2,218,281)(H2,219,282)(H2,220,283)(H2,221,290)(H,230,237)(H,235,295)(H,236,296)(H,238,291)(H,239,297)(H,240,310)(H,241,284)(H,242,315)(H,243,302)(H,244,301)(H,245,298)(H,246,307)(H,247,311)(H,248,312)(H,249,318)(H,250,300)(H,251,299)(H,252,308)(H,253,321)(H,254,322)(H,255,313)(H,256,305)(H,257,306)(H,258,303)(H,259,320)(H,260,304)(H,261,319)(H,262,323)(H,263,324)(H,264,325)(H,265,294)(H,266,314)(H,267,316)(H,268,285)(H,269,293)(H,270,292)(H,271,309)(H,272,317)(H,286,287)(H,288,289)(H4,222,223,231)(H4,224,225,232)(H4,226,227,233)(H4,228,229,234)/t113-,114-,115-,116-,117+,130-,131-,132-,133-,134-,135-,136-,137-,138-,139-,140-,141-,142-,143-,144-,145-,146-,147-,148-,149-,150-,151-,152-,153-,154-,155-,156-,157-,165-,166-,167-,168-,169-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 5.40n/an/an/an/an/an/a



Institut National de la Recherche Scientifique

Curated by ChEMBL


Assay Description
Displacement of [125I]Ac-PACAP27 from human recombinant PAC1 receptor expressed in CHO cells by gamma- counter


J Med Chem 52: 3308-16 (2009)


Article DOI: 10.1021/jm900291j
BindingDB Entry DOI: 10.7270/Q29023PC
More data for this
Ligand-Target Pair
Pituitary adenylate cyclase-activating polypeptide type I receptor


(Homo sapiens (Human))
BDBM50250075
PNG
(CHEMBL526315 | [Bip6]PACAP38)
Show SMILES CC[C@H](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](Cc1ccc(cc1)-c1ccccc1)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](CCCNC(N)=N)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCCCN)C(N)=O |r|
Show InChI InChI=1S/C209H335N63O53S/c1-18-113(12)168(268-162(285)103-236-176(296)153(99-163(286)287)261-199(319)155(104-273)265-174(294)130(217)97-125-101-230-107-237-125)204(324)263-151(92-118-53-63-124(64-54-118)123-40-20-19-21-41-123)197(317)272-169(117(16)276)205(325)264-154(100-164(288)289)196(316)267-157(106-275)200(320)259-150(96-122-61-71-129(280)72-62-122)194(314)266-156(105-274)198(318)249-140(51-38-87-233-208(226)227)186(306)257-148(94-120-57-67-127(278)68-58-120)192(312)248-138(49-36-85-231-206(222)223)182(302)243-133(44-24-31-80-212)179(299)251-143(74-76-159(219)282)188(308)252-144(77-89-326-17)177(297)239-116(15)173(293)269-165(110(6)7)201(321)253-136(47-27-34-83-215)181(301)244-135(46-26-33-82-214)183(303)258-149(95-121-59-69-128(279)70-60-121)193(313)255-146(91-109(4)5)190(310)240-114(13)171(291)238-115(14)172(292)270-166(111(8)9)203(323)262-145(90-108(2)3)175(295)235-102-161(284)241-132(43-23-30-79-211)178(298)245-139(50-37-86-232-207(224)225)185(305)256-147(93-119-55-65-126(277)66-56-119)191(311)247-134(45-25-32-81-213)180(300)250-142(73-75-158(218)281)187(307)246-141(52-39-88-234-209(228)229)189(309)271-167(112(10)11)202(322)254-137(48-28-35-84-216)184(304)260-152(98-160(220)283)195(315)242-131(170(221)290)42-22-29-78-210/h19-21,40-41,53-72,101,107-117,130-157,165-169,273-280H,18,22-39,42-52,73-100,102-106,210-217H2,1-17H3,(H2,218,281)(H2,219,282)(H2,220,283)(H2,221,290)(H,230,237)(H,235,295)(H,236,296)(H,238,291)(H,239,297)(H,240,310)(H,241,284)(H,242,315)(H,243,302)(H,244,301)(H,245,298)(H,246,307)(H,247,311)(H,248,312)(H,249,318)(H,250,300)(H,251,299)(H,252,308)(H,253,321)(H,254,322)(H,255,313)(H,256,305)(H,257,306)(H,258,303)(H,259,320)(H,260,304)(H,261,319)(H,262,323)(H,263,324)(H,264,325)(H,265,294)(H,266,314)(H,267,316)(H,268,285)(H,269,293)(H,270,292)(H,271,309)(H,272,317)(H,286,287)(H,288,289)(H4,222,223,231)(H4,224,225,232)(H4,226,227,233)(H4,228,229,234)/t113-,114-,115-,116-,117+,130-,131-,132-,133-,134-,135-,136-,137-,138-,139-,140-,141-,142-,143-,144-,145-,146-,147-,148-,149-,150-,151-,152-,153-,154-,155-,156-,157-,165-,166-,167-,168-,169-/m0/s1
PDB

Reactome pathway
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 1.10n/an/an/an/a



Institut National de la Recherche Scientifique

Curated by ChEMBL


Assay Description
Agonist activity at human recombinant PAC1 receptor expressed in CHO cells assessed as PACAP38-induced calcium mobilization by FLIPR assay


J Med Chem 52: 3308-16 (2009)


Article DOI: 10.1021/jm900291j
BindingDB Entry DOI: 10.7270/Q29023PC
More data for this
Ligand-Target Pair