Found 2 hits for monomerid = 50183898 Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
Glucagon-like peptide 2 receptor
(Homo sapiens (Human)) | BDBM50183898
![PNG](/data/jpeg/tenK5018/BindingDB_50183898.png) (CHEMBL3824179)Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)CC)[C@@H](C)CC)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(N)=O |r| Show InChI InChI=1S/C150H230N42O48S/c1-18-72(10)117(145(236)174-88(40-42-106(153)197)130(221)191-120(77(15)195)148(239)170-86(122(157)213)38-29-30-45-151)188-140(231)93(50-71(8)9)176-134(225)96(53-81-62-162-85-37-28-27-36-83(81)85)179-136(227)98(56-108(155)199)186-146(237)118(73(11)19-2)189-141(232)95(52-80-34-25-22-26-35-80)177-138(229)102(60-115(209)210)182-127(218)87(39-31-46-161-150(158)159)171-124(215)76(14)166-123(214)75(13)167-131(222)91(48-69(4)5)175-135(226)97(55-107(154)198)181-139(230)103(61-116(211)212)183-132(223)92(49-70(6)7)185-147(238)119(74(12)20-3)190-149(240)121(78(16)196)192-142(233)99(57-109(156)200)180-129(220)90(44-47-241-17)173-128(219)89(41-43-112(203)204)172-137(228)101(59-114(207)208)184-144(235)105(67-194)187-133(224)94(51-79-32-23-21-24-33-79)178-143(234)104(66-193)169-111(202)65-164-126(217)100(58-113(205)206)168-110(201)64-163-125(216)84(152)54-82-63-160-68-165-82/h21-28,32-37,62-63,68-78,84,86-105,117-121,162,193-196H,18-20,29-31,38-61,64-67,151-152H2,1-17H3,(H2,153,197)(H2,154,198)(H2,155,199)(H2,156,200)(H2,157,213)(H,160,165)(H,163,216)(H,164,217)(H,166,214)(H,167,222)(H,168,201)(H,169,202)(H,170,239)(H,171,215)(H,172,228)(H,173,219)(H,174,236)(H,175,226)(H,176,225)(H,177,229)(H,178,234)(H,179,227)(H,180,220)(H,181,230)(H,182,218)(H,183,223)(H,184,235)(H,185,238)(H,186,237)(H,187,224)(H,188,231)(H,189,232)(H,190,240)(H,191,221)(H,192,233)(H,203,204)(H,205,206)(H,207,208)(H,209,210)(H,211,212)(H4,158,159,161)/t72-,73-,74-,75-,76-,77+,78+,84-,86-,87-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,117-,118-,119-,120-,121-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt UniProtKB/TrEMBL
DrugBank antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | n/a | n/a | 0.220 | n/a | n/a | n/a | n/a |
Ferring Research Institute Inc.
Curated by ChEMBL
| Assay Description Agonist activity at human GLP2R expressed in HEK293 cells after 5 hrs by luciferase reporter gene assay |
J Med Chem 59: 3129-39 (2016)
BindingDB Entry DOI: 10.7270/Q23R0VT7 |
More data for this Ligand-Target Pair | |
Glucagon-like peptide 1 receptor (GLP-1)
(Homo sapiens (Human)) | BDBM50183898
![PNG](/data/jpeg/tenK5018/BindingDB_50183898.png) (CHEMBL3824179)Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCCNC(N)=N)NC(=O)[C@H](C)NC(=O)[C@H](C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCSC)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](CO)NC(=O)CNC(=O)[C@H](CC(O)=O)NC(=O)CNC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)CC)[C@@H](C)CC)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CCCCN)C(N)=O |r| Show InChI InChI=1S/C150H230N42O48S/c1-18-72(10)117(145(236)174-88(40-42-106(153)197)130(221)191-120(77(15)195)148(239)170-86(122(157)213)38-29-30-45-151)188-140(231)93(50-71(8)9)176-134(225)96(53-81-62-162-85-37-28-27-36-83(81)85)179-136(227)98(56-108(155)199)186-146(237)118(73(11)19-2)189-141(232)95(52-80-34-25-22-26-35-80)177-138(229)102(60-115(209)210)182-127(218)87(39-31-46-161-150(158)159)171-124(215)76(14)166-123(214)75(13)167-131(222)91(48-69(4)5)175-135(226)97(55-107(154)198)181-139(230)103(61-116(211)212)183-132(223)92(49-70(6)7)185-147(238)119(74(12)20-3)190-149(240)121(78(16)196)192-142(233)99(57-109(156)200)180-129(220)90(44-47-241-17)173-128(219)89(41-43-112(203)204)172-137(228)101(59-114(207)208)184-144(235)105(67-194)187-133(224)94(51-79-32-23-21-24-33-79)178-143(234)104(66-193)169-111(202)65-164-126(217)100(58-113(205)206)168-110(201)64-163-125(216)84(152)54-82-63-160-68-165-82/h21-28,32-37,62-63,68-78,84,86-105,117-121,162,193-196H,18-20,29-31,38-61,64-67,151-152H2,1-17H3,(H2,153,197)(H2,154,198)(H2,155,199)(H2,156,200)(H2,157,213)(H,160,165)(H,163,216)(H,164,217)(H,166,214)(H,167,222)(H,168,201)(H,169,202)(H,170,239)(H,171,215)(H,172,228)(H,173,219)(H,174,236)(H,175,226)(H,176,225)(H,177,229)(H,178,234)(H,179,227)(H,180,220)(H,181,230)(H,182,218)(H,183,223)(H,184,235)(H,185,238)(H,186,237)(H,187,224)(H,188,231)(H,189,232)(H,190,240)(H,191,221)(H,192,233)(H,203,204)(H,205,206)(H,207,208)(H,209,210)(H,211,212)(H4,158,159,161)/t72-,73-,74-,75-,76-,77+,78+,84-,86-,87-,88-,89-,90-,91-,92-,93-,94-,95-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,117-,118-,119-,120-,121-/m0/s1 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet ![](/images/AffyNet_logo.png)
| CHEMBL PC cid PC sid UniChem
Similars
| PubMed
| n/a | n/a | n/a | n/a | >1.00E+3 | n/a | n/a | n/a | n/a |
Ferring Research Institute Inc.
Curated by ChEMBL
| Assay Description Agonist activity at human GLP1R expressed in HEK293 cells after 5 hrs by luciferase reporter gene assay |
J Med Chem 59: 3129-39 (2016)
BindingDB Entry DOI: 10.7270/Q23R0VT7 |
More data for this Ligand-Target Pair | |