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BDBM50005109 CHEMBL3086660

SMILES: CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCCN)NC(=O)C(NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)Cc1ccc(O)cc1)C(C)(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)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](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O

InChI Key: InChIKey=YWAKQNOYBHASNB-QYEWQHDOSA-N

Data: 1 KI

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50005109   
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
Dipeptidyl peptidase 4


(Homo sapiens (Human))
BDBM50005109
PNG
(CHEMBL3086660)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=O)[C@H](CCSC)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](C)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)CNC(=O)[C@@H]1CCCN1C(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCCN)NC(=O)C(NC(=O)[C@@H]1CCCN1C(=O)[C@@H](N)Cc1ccc(O)cc1)C(C)(C)C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(C)C)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](CCCNC(N)=N)C(=O)N[C@@H](Cc1ccc(O)cc1)C(N)=O |r|
Show InChI InChI=1S/C192H290N54O55S/c1-18-97(8)150(180(294)236-131(85-142(195)254)169(283)227-125(77-95(4)5)165(279)228-126(78-96(6)7)172(286)240-151(102(13)248)181(295)223-122(34-24-69-210-191(204)205)186(300)245-73-28-37-139(245)177(291)222-117(33-23-68-209-190(202)203)158(272)225-123(153(197)267)80-104-42-52-110(250)53-43-104)239-173(287)129(83-107-48-58-113(253)59-49-107)231-168(282)130(84-108-90-206-93-212-108)232-160(274)116(32-22-67-208-189(200)201)220-164(278)124(76-94(2)3)226-156(270)99(10)214-174(288)136(92-247)238-167(281)128(82-106-46-56-112(252)57-47-106)230-166(280)127(81-105-44-54-111(251)55-45-105)229-159(273)115(31-21-66-207-188(198)199)218-154(268)98(9)213-157(271)120(64-75-302-17)221-170(284)133(88-148(263)264)234-162(276)119(61-63-146(259)260)219-155(269)100(11)215-176(290)138-36-26-70-242(138)183(297)101(12)216-163(277)132(87-147(261)262)233-161(275)118(60-62-145(257)258)217-144(256)91-211-175(289)137-35-25-72-244(137)187(301)135(86-143(196)255)237-171(285)134(89-149(265)266)235-178(292)140-38-29-74-246(140)185(299)121(30-19-20-65-193)224-182(296)152(192(14,15)16)241-179(293)141-39-27-71-243(141)184(298)114(194)79-103-40-50-109(249)51-41-103/h40-59,90,93-102,114-141,150-152,247-253H,18-39,60-89,91-92,193-194H2,1-17H3,(H2,195,254)(H2,196,255)(H2,197,267)(H,206,212)(H,211,289)(H,213,271)(H,214,288)(H,215,290)(H,216,277)(H,217,256)(H,218,268)(H,219,269)(H,220,278)(H,221,284)(H,222,291)(H,223,295)(H,224,296)(H,225,272)(H,226,270)(H,227,283)(H,228,279)(H,229,273)(H,230,280)(H,231,282)(H,232,274)(H,233,275)(H,234,276)(H,235,292)(H,236,294)(H,237,285)(H,238,281)(H,239,287)(H,240,286)(H,241,293)(H,257,258)(H,259,260)(H,261,262)(H,263,264)(H,265,266)(H4,198,199,207)(H4,200,201,208)(H4,202,203,209)(H4,204,205,210)/t97-,98-,99-,100-,101-,102+,114-,115-,116-,117-,118-,119-,120-,121-,122-,123-,124-,125-,126-,127-,128-,129-,130-,131-,132-,133-,134-,135-,136-,137-,138-,139-,140-,141-,150-,151-,152?/m0/s1
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
5.00E+3n/an/an/an/an/an/an/an/a



Tufts University

Curated by ChEMBL


Assay Description
Competitive inhibition of human recombinant DPP4 using AP-pNA as substrate preincubated for 30 mins followed by substrate addition measured after 30 ...


J Med Chem 56: 8339-51 (2013)


Article DOI: 10.1021/jm400423p
BindingDB Entry DOI: 10.7270/Q2PK0HMZ
More data for this
Ligand-Target Pair