BindingDB logo
myBDB logout

BDBM50273764 (4S,7S,10S,13S,16S,22S,25S,28S,31S,34S,37S,40S,43S,46S,49S,52S,58S)-4-((6S,12S,15S,18S,21S,24S,27S,30S,31S)-21-((1H-indol-3-yl)methyl)-1-amino-12-(4-aminobutyl)-27-benzyl-6-carbamoyl-1-imino-18-isobutyl-15-isopropyl-24,31-dimethyl-8,11,14,17,20,23,26,29-octaoxo-2,7,10,13,16,19,22,25,28-nonaazatritriacontan-30-ylcarbamoyl)-22-(4-acetamidobutyl)-58-((S)-2-((S)-2-amino-3-(1H-imidazol-5-yl)propanamido)propanamido)-10,16-bis(3-amino-3-oxopropyl)-7-(4-aminobutyl)-49-benzyl-40-(carboxymethyl)-28-(4-hyd::CHEMBL500483

SMILES: CC[C@H](C)[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCCCNC(C)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCN=C(N)N)C(N)=O

InChI Key: InChIKey=DYYIVFGWEORZKN-VOKUODBCSA-N

Data: 2 IC50  1 EC50

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 3 hits for monomerid = 50273764   
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
Glucagon-like peptide 1 receptor (GLP-1)


(Homo sapiens (Human))
BDBM50273764
PNG
((4S,7S,10S,13S,16S,22S,25S,28S,31S,34S,37S,40S,43S...)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCCCNC(C)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCN=C(N)N)C(N)=O |r,wU:152.154,138.145,130.132,160.164,115.116,163.167,101.106,91.94,73.82,53.61,40.45,26.31,8.13,2.2,172.174,188.191,210.215,wD:147.149,119.128,109.112,97.98,85.88,65.69,35.35,17.22,4.4,183.187,202.207,217.222,230.235,(75.33,-7.95,;75.33,-6.4,;76.66,-5.64,;78,-6.41,;76.66,-4.1,;75.33,-3.33,;73.99,-4.1,;73.99,-5.64,;72.66,-3.33,;72.66,-1.79,;73.99,-1.02,;73.99,.52,;72.65,1.29,;75.32,1.29,;71.33,-4.11,;69.99,-3.34,;69.99,-1.8,;68.65,-4.1,;68.65,-5.64,;69.99,-6.41,;69.99,-7.95,;71.33,-8.73,;71.33,-10.26,;67.33,-3.34,;65.99,-4.11,;65.99,-5.65,;64.66,-3.35,;64.66,-1.8,;65.99,-1.03,;65.99,.52,;64.65,1.29,;67.32,1.28,;63.32,-4.12,;61.99,-3.34,;61.99,-1.8,;60.65,-4.12,;60.65,-5.66,;59.33,-3.35,;57.98,-4.12,;57.98,-5.66,;56.66,-3.35,;56.66,-1.81,;57.98,-1.04,;57.98,.5,;56.65,1.28,;59.32,1.27,;55.32,-4.12,;53.99,-3.36,;53.99,-1.81,;52.65,-4.13,;51.32,-3.36,;49.98,-4.13,;49.98,-5.67,;48.65,-3.36,;48.65,-1.82,;49.98,-1.05,;49.98,.49,;51.32,1.26,;51.32,2.81,;52.65,3.57,;52.65,5.11,;53.98,2.81,;47.32,-4.14,;45.98,-3.37,;45.98,-1.83,;44.65,-4.14,;44.65,-5.67,;45.98,-6.44,;45.98,-7.98,;47.32,-5.67,;43.31,-3.37,;41.98,-4.14,;41.98,-5.68,;40.65,-3.38,;40.65,-1.83,;41.98,-1.06,;43.31,-1.83,;44.64,-1.05,;44.64,.48,;45.98,1.26,;43.31,1.25,;41.98,.48,;39.31,-4.15,;37.99,-3.37,;37.99,-1.83,;36.65,-4.15,;36.65,-5.69,;37.99,-6.46,;35.31,-3.38,;33.98,-4.15,;33.98,-5.69,;32.65,-3.38,;32.65,-1.84,;33.98,-1.07,;31.31,-4.15,;29.98,-3.39,;29.98,-1.84,;28.64,-4.16,;27.31,-3.39,;25.98,-4.16,;25.98,-5.7,;24.64,-3.39,;24.64,-1.85,;25.98,-1.09,;27.31,-1.85,;25.98,.46,;23.31,-4.17,;21.98,-3.4,;21.98,-1.86,;20.64,-4.17,;20.64,-5.7,;21.98,-6.48,;19.31,-3.4,;17.97,-4.17,;17.97,-5.71,;16.64,-3.41,;15.31,-4.18,;13.97,-3.41,;13.97,-1.86,;12.64,-4.18,;12.64,-5.72,;13.97,-6.49,;15.3,-5.71,;16.64,-6.48,;16.65,-8.02,;15.31,-8.79,;13.98,-8.02,;11.31,-3.41,;9.97,-4.19,;9.97,-5.72,;8.64,-3.41,;7.3,-4.18,;5.97,-3.42,;5.97,-1.87,;4.64,-4.19,;3.31,-3.42,;1.97,-4.19,;1.97,-5.73,;.64,-3.42,;.64,-1.88,;1.97,-1.12,;1.97,.43,;.63,1.2,;3.3,1.2,;-.7,-4.2,;-2.03,-3.42,;-2.03,-1.89,;-3.37,-4.2,;-3.37,-5.73,;-4.7,-3.43,;-6.03,-4.19,;-6.03,-5.74,;-7.37,-3.43,;-8.71,-4.2,;-7.37,-1.89,;-6.03,-1.12,;-4.63,-1.74,;-3.6,-.6,;-4.37,.73,;-5.87,.41,;8.64,-1.87,;7.3,-1.09,;9.97,-1.1,;16.64,-1.86,;15.31,-1.09,;17.97,-1.09,;28.64,-5.7,;29.98,-6.47,;27.31,-6.46,;78,-3.33,;78,-1.78,;79.32,-4.09,;80.66,-3.32,;80.66,-1.78,;82,-1.01,;83.33,-1.78,;84.66,-1.01,;84.66,.53,;83.32,1.3,;81.99,.53,;82,-4.09,;82,-5.63,;83.33,-3.32,;84.66,-4.09,;84.66,-5.63,;86,-3.31,;86,-1.77,;87.33,-4.09,;88.67,-3.32,;88.67,-1.78,;90,-1,;91.4,-1.62,;92.43,-.47,;91.66,.85,;92.14,2.32,;91.11,3.46,;89.6,3.14,;89.13,1.67,;90.16,.53,;90,-4.08,;90,-5.62,;91.33,-3.31,;92.67,-4.08,;92.67,-5.62,;94,-6.38,;94,-7.92,;95.34,-5.62,;94,-3.3,;94,-1.76,;95.33,-4.08,;96.67,-3.31,;96.67,-1.76,;98,-.99,;95.33,-.99,;98,-4.07,;98,-5.61,;99.34,-3.3,;100.67,-4.07,;100.67,-5.61,;102,-6.38,;102,-7.91,;103.34,-8.68,;103.34,-10.22,;102,-3.3,;102,-1.76,;103.34,-4.06,;104.67,-3.29,;106,-4.07,;106,-5.6,;107.34,-3.29,;108.67,-4.06,;108.67,-5.6,;110.01,-6.37,;110.01,-7.91,;111.35,-8.68,;111.35,-10.21,;110.01,-10.98,;112.68,-10.98,;110.01,-3.29,;111.34,-4.05,;110.01,-1.74,)|
Show InChI InChI=1S/C154H236N42O45/c1-17-80(10)124(151(239)187-106(61-87-33-20-18-21-34-87)139(227)173-83(13)130(218)182-109(64-90-67-166-95-38-25-24-37-93(90)95)142(230)184-105(60-77(4)5)143(231)193-122(78(6)7)149(237)181-98(39-26-29-55-155)133(221)167-69-116(206)174-96(127(160)215)42-32-58-165-154(161)162)195-138(226)103(50-54-120(211)212)180-136(224)99(40-27-30-56-156)179-137(225)102(48-52-115(159)205)177-129(217)82(12)172-135(223)101(47-51-114(158)204)175-117(207)70-168-132(220)97(41-28-31-57-164-86(16)202)178-140(228)104(59-76(2)3)183-141(229)107(63-89-43-45-92(203)46-44-89)185-146(234)111(72-197)189-148(236)113(74-199)190-150(238)123(79(8)9)194-145(233)110(66-121(213)214)186-147(235)112(73-198)191-153(241)126(85(15)201)196-144(232)108(62-88-35-22-19-23-36-88)188-152(240)125(84(14)200)192-118(208)71-169-134(222)100(49-53-119(209)210)176-128(216)81(11)171-131(219)94(157)65-91-68-163-75-170-91/h18-25,33-38,43-46,67-68,75-85,94,96-113,122-126,166,197-201,203H,17,26-32,39-42,47-66,69-74,155-157H2,1-16H3,(H2,158,204)(H2,159,205)(H2,160,215)(H,163,170)(H,164,202)(H,167,221)(H,168,220)(H,169,222)(H,171,219)(H,172,223)(H,173,227)(H,174,206)(H,175,207)(H,176,216)(H,177,217)(H,178,228)(H,179,225)(H,180,224)(H,181,237)(H,182,218)(H,183,229)(H,184,230)(H,185,234)(H,186,235)(H,187,239)(H,188,240)(H,189,236)(H,190,238)(H,191,241)(H,192,208)(H,193,231)(H,194,233)(H,195,226)(H,196,232)(H,209,210)(H,211,212)(H,213,214)(H4,161,162,165)/t80-,81-,82-,83-,84+,85+,94-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,122-,123-,124-,125-,126-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.60E+3n/an/an/an/an/an/a



University of Texas at Dallas

Curated by ChEMBL


Assay Description
Displacement of [125I]exendin(9-39) from human GLP1R expressed in HEK293 cells


Bioorg Med Chem 16: 10106-12 (2008)


Article DOI: 10.1016/j.bmc.2008.10.006
BindingDB Entry DOI: 10.7270/Q2B857ZT
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor (GLP-1)


(Homo sapiens (Human))
BDBM50273764
PNG
((4S,7S,10S,13S,16S,22S,25S,28S,31S,34S,37S,40S,43S...)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCCCNC(C)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCN=C(N)N)C(N)=O |r,wU:152.154,138.145,130.132,160.164,115.116,163.167,101.106,91.94,73.82,53.61,40.45,26.31,8.13,2.2,172.174,188.191,210.215,wD:147.149,119.128,109.112,97.98,85.88,65.69,35.35,17.22,4.4,183.187,202.207,217.222,230.235,(75.33,-7.95,;75.33,-6.4,;76.66,-5.64,;78,-6.41,;76.66,-4.1,;75.33,-3.33,;73.99,-4.1,;73.99,-5.64,;72.66,-3.33,;72.66,-1.79,;73.99,-1.02,;73.99,.52,;72.65,1.29,;75.32,1.29,;71.33,-4.11,;69.99,-3.34,;69.99,-1.8,;68.65,-4.1,;68.65,-5.64,;69.99,-6.41,;69.99,-7.95,;71.33,-8.73,;71.33,-10.26,;67.33,-3.34,;65.99,-4.11,;65.99,-5.65,;64.66,-3.35,;64.66,-1.8,;65.99,-1.03,;65.99,.52,;64.65,1.29,;67.32,1.28,;63.32,-4.12,;61.99,-3.34,;61.99,-1.8,;60.65,-4.12,;60.65,-5.66,;59.33,-3.35,;57.98,-4.12,;57.98,-5.66,;56.66,-3.35,;56.66,-1.81,;57.98,-1.04,;57.98,.5,;56.65,1.28,;59.32,1.27,;55.32,-4.12,;53.99,-3.36,;53.99,-1.81,;52.65,-4.13,;51.32,-3.36,;49.98,-4.13,;49.98,-5.67,;48.65,-3.36,;48.65,-1.82,;49.98,-1.05,;49.98,.49,;51.32,1.26,;51.32,2.81,;52.65,3.57,;52.65,5.11,;53.98,2.81,;47.32,-4.14,;45.98,-3.37,;45.98,-1.83,;44.65,-4.14,;44.65,-5.67,;45.98,-6.44,;45.98,-7.98,;47.32,-5.67,;43.31,-3.37,;41.98,-4.14,;41.98,-5.68,;40.65,-3.38,;40.65,-1.83,;41.98,-1.06,;43.31,-1.83,;44.64,-1.05,;44.64,.48,;45.98,1.26,;43.31,1.25,;41.98,.48,;39.31,-4.15,;37.99,-3.37,;37.99,-1.83,;36.65,-4.15,;36.65,-5.69,;37.99,-6.46,;35.31,-3.38,;33.98,-4.15,;33.98,-5.69,;32.65,-3.38,;32.65,-1.84,;33.98,-1.07,;31.31,-4.15,;29.98,-3.39,;29.98,-1.84,;28.64,-4.16,;27.31,-3.39,;25.98,-4.16,;25.98,-5.7,;24.64,-3.39,;24.64,-1.85,;25.98,-1.09,;27.31,-1.85,;25.98,.46,;23.31,-4.17,;21.98,-3.4,;21.98,-1.86,;20.64,-4.17,;20.64,-5.7,;21.98,-6.48,;19.31,-3.4,;17.97,-4.17,;17.97,-5.71,;16.64,-3.41,;15.31,-4.18,;13.97,-3.41,;13.97,-1.86,;12.64,-4.18,;12.64,-5.72,;13.97,-6.49,;15.3,-5.71,;16.64,-6.48,;16.65,-8.02,;15.31,-8.79,;13.98,-8.02,;11.31,-3.41,;9.97,-4.19,;9.97,-5.72,;8.64,-3.41,;7.3,-4.18,;5.97,-3.42,;5.97,-1.87,;4.64,-4.19,;3.31,-3.42,;1.97,-4.19,;1.97,-5.73,;.64,-3.42,;.64,-1.88,;1.97,-1.12,;1.97,.43,;.63,1.2,;3.3,1.2,;-.7,-4.2,;-2.03,-3.42,;-2.03,-1.89,;-3.37,-4.2,;-3.37,-5.73,;-4.7,-3.43,;-6.03,-4.19,;-6.03,-5.74,;-7.37,-3.43,;-8.71,-4.2,;-7.37,-1.89,;-6.03,-1.12,;-4.63,-1.74,;-3.6,-.6,;-4.37,.73,;-5.87,.41,;8.64,-1.87,;7.3,-1.09,;9.97,-1.1,;16.64,-1.86,;15.31,-1.09,;17.97,-1.09,;28.64,-5.7,;29.98,-6.47,;27.31,-6.46,;78,-3.33,;78,-1.78,;79.32,-4.09,;80.66,-3.32,;80.66,-1.78,;82,-1.01,;83.33,-1.78,;84.66,-1.01,;84.66,.53,;83.32,1.3,;81.99,.53,;82,-4.09,;82,-5.63,;83.33,-3.32,;84.66,-4.09,;84.66,-5.63,;86,-3.31,;86,-1.77,;87.33,-4.09,;88.67,-3.32,;88.67,-1.78,;90,-1,;91.4,-1.62,;92.43,-.47,;91.66,.85,;92.14,2.32,;91.11,3.46,;89.6,3.14,;89.13,1.67,;90.16,.53,;90,-4.08,;90,-5.62,;91.33,-3.31,;92.67,-4.08,;92.67,-5.62,;94,-6.38,;94,-7.92,;95.34,-5.62,;94,-3.3,;94,-1.76,;95.33,-4.08,;96.67,-3.31,;96.67,-1.76,;98,-.99,;95.33,-.99,;98,-4.07,;98,-5.61,;99.34,-3.3,;100.67,-4.07,;100.67,-5.61,;102,-6.38,;102,-7.91,;103.34,-8.68,;103.34,-10.22,;102,-3.3,;102,-1.76,;103.34,-4.06,;104.67,-3.29,;106,-4.07,;106,-5.6,;107.34,-3.29,;108.67,-4.06,;108.67,-5.6,;110.01,-6.37,;110.01,-7.91,;111.35,-8.68,;111.35,-10.21,;110.01,-10.98,;112.68,-10.98,;110.01,-3.29,;111.34,-4.05,;110.01,-1.74,)|
Show InChI InChI=1S/C154H236N42O45/c1-17-80(10)124(151(239)187-106(61-87-33-20-18-21-34-87)139(227)173-83(13)130(218)182-109(64-90-67-166-95-38-25-24-37-93(90)95)142(230)184-105(60-77(4)5)143(231)193-122(78(6)7)149(237)181-98(39-26-29-55-155)133(221)167-69-116(206)174-96(127(160)215)42-32-58-165-154(161)162)195-138(226)103(50-54-120(211)212)180-136(224)99(40-27-30-56-156)179-137(225)102(48-52-115(159)205)177-129(217)82(12)172-135(223)101(47-51-114(158)204)175-117(207)70-168-132(220)97(41-28-31-57-164-86(16)202)178-140(228)104(59-76(2)3)183-141(229)107(63-89-43-45-92(203)46-44-89)185-146(234)111(72-197)189-148(236)113(74-199)190-150(238)123(79(8)9)194-145(233)110(66-121(213)214)186-147(235)112(73-198)191-153(241)126(85(15)201)196-144(232)108(62-88-35-22-19-23-36-88)188-152(240)125(84(14)200)192-118(208)71-169-134(222)100(49-53-119(209)210)176-128(216)81(11)171-131(219)94(157)65-91-68-163-75-170-91/h18-25,33-38,43-46,67-68,75-85,94,96-113,122-126,166,197-201,203H,17,26-32,39-42,47-66,69-74,155-157H2,1-16H3,(H2,158,204)(H2,159,205)(H2,160,215)(H,163,170)(H,164,202)(H,167,221)(H,168,220)(H,169,222)(H,171,219)(H,172,223)(H,173,227)(H,174,206)(H,175,207)(H,176,216)(H,177,217)(H,178,228)(H,179,225)(H,180,224)(H,181,237)(H,182,218)(H,183,229)(H,184,230)(H,185,234)(H,186,235)(H,187,239)(H,188,240)(H,189,236)(H,190,238)(H,191,241)(H,192,208)(H,193,231)(H,194,233)(H,195,226)(H,196,232)(H,209,210)(H,211,212)(H,213,214)(H4,161,162,165)/t80-,81-,82-,83-,84+,85+,94-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,122-,123-,124-,125-,126-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/an/an/a 0.123n/an/an/an/a



University of Texas at Dallas

Curated by ChEMBL


Assay Description
Activation of human GLP1R expressed in HEK293 cells assessed as effect on cAMP responsive element promoter driven luciferase expression


Bioorg Med Chem 16: 10106-12 (2008)


Article DOI: 10.1016/j.bmc.2008.10.006
BindingDB Entry DOI: 10.7270/Q2B857ZT
More data for this
Ligand-Target Pair
Glucagon-like peptide 1 receptor (GLP-1)


(Homo sapiens (Human))
BDBM50273764
PNG
((4S,7S,10S,13S,16S,22S,25S,28S,31S,34S,37S,40S,43S...)
Show SMILES CC[C@H](C)[C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)CNC(=O)[C@H](CCCCNC(C)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)[C@H](CO)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](CC(O)=O)NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)CNC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](C)NC(=O)[C@@H](N)Cc1cnc[nH]1)[C@@H](C)O)[C@@H](C)O)C(C)C)C(=O)N[C@@H](Cc1ccccc1)C(=O)N[C@@H](C)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C(C)C)C(=O)N[C@@H](CCCCN)C(=O)NCC(=O)N[C@@H](CCCN=C(N)N)C(N)=O |r,wU:152.154,138.145,130.132,160.164,115.116,163.167,101.106,91.94,73.82,53.61,40.45,26.31,8.13,2.2,172.174,188.191,210.215,wD:147.149,119.128,109.112,97.98,85.88,65.69,35.35,17.22,4.4,183.187,202.207,217.222,230.235,(75.33,-7.95,;75.33,-6.4,;76.66,-5.64,;78,-6.41,;76.66,-4.1,;75.33,-3.33,;73.99,-4.1,;73.99,-5.64,;72.66,-3.33,;72.66,-1.79,;73.99,-1.02,;73.99,.52,;72.65,1.29,;75.32,1.29,;71.33,-4.11,;69.99,-3.34,;69.99,-1.8,;68.65,-4.1,;68.65,-5.64,;69.99,-6.41,;69.99,-7.95,;71.33,-8.73,;71.33,-10.26,;67.33,-3.34,;65.99,-4.11,;65.99,-5.65,;64.66,-3.35,;64.66,-1.8,;65.99,-1.03,;65.99,.52,;64.65,1.29,;67.32,1.28,;63.32,-4.12,;61.99,-3.34,;61.99,-1.8,;60.65,-4.12,;60.65,-5.66,;59.33,-3.35,;57.98,-4.12,;57.98,-5.66,;56.66,-3.35,;56.66,-1.81,;57.98,-1.04,;57.98,.5,;56.65,1.28,;59.32,1.27,;55.32,-4.12,;53.99,-3.36,;53.99,-1.81,;52.65,-4.13,;51.32,-3.36,;49.98,-4.13,;49.98,-5.67,;48.65,-3.36,;48.65,-1.82,;49.98,-1.05,;49.98,.49,;51.32,1.26,;51.32,2.81,;52.65,3.57,;52.65,5.11,;53.98,2.81,;47.32,-4.14,;45.98,-3.37,;45.98,-1.83,;44.65,-4.14,;44.65,-5.67,;45.98,-6.44,;45.98,-7.98,;47.32,-5.67,;43.31,-3.37,;41.98,-4.14,;41.98,-5.68,;40.65,-3.38,;40.65,-1.83,;41.98,-1.06,;43.31,-1.83,;44.64,-1.05,;44.64,.48,;45.98,1.26,;43.31,1.25,;41.98,.48,;39.31,-4.15,;37.99,-3.37,;37.99,-1.83,;36.65,-4.15,;36.65,-5.69,;37.99,-6.46,;35.31,-3.38,;33.98,-4.15,;33.98,-5.69,;32.65,-3.38,;32.65,-1.84,;33.98,-1.07,;31.31,-4.15,;29.98,-3.39,;29.98,-1.84,;28.64,-4.16,;27.31,-3.39,;25.98,-4.16,;25.98,-5.7,;24.64,-3.39,;24.64,-1.85,;25.98,-1.09,;27.31,-1.85,;25.98,.46,;23.31,-4.17,;21.98,-3.4,;21.98,-1.86,;20.64,-4.17,;20.64,-5.7,;21.98,-6.48,;19.31,-3.4,;17.97,-4.17,;17.97,-5.71,;16.64,-3.41,;15.31,-4.18,;13.97,-3.41,;13.97,-1.86,;12.64,-4.18,;12.64,-5.72,;13.97,-6.49,;15.3,-5.71,;16.64,-6.48,;16.65,-8.02,;15.31,-8.79,;13.98,-8.02,;11.31,-3.41,;9.97,-4.19,;9.97,-5.72,;8.64,-3.41,;7.3,-4.18,;5.97,-3.42,;5.97,-1.87,;4.64,-4.19,;3.31,-3.42,;1.97,-4.19,;1.97,-5.73,;.64,-3.42,;.64,-1.88,;1.97,-1.12,;1.97,.43,;.63,1.2,;3.3,1.2,;-.7,-4.2,;-2.03,-3.42,;-2.03,-1.89,;-3.37,-4.2,;-3.37,-5.73,;-4.7,-3.43,;-6.03,-4.19,;-6.03,-5.74,;-7.37,-3.43,;-8.71,-4.2,;-7.37,-1.89,;-6.03,-1.12,;-4.63,-1.74,;-3.6,-.6,;-4.37,.73,;-5.87,.41,;8.64,-1.87,;7.3,-1.09,;9.97,-1.1,;16.64,-1.86,;15.31,-1.09,;17.97,-1.09,;28.64,-5.7,;29.98,-6.47,;27.31,-6.46,;78,-3.33,;78,-1.78,;79.32,-4.09,;80.66,-3.32,;80.66,-1.78,;82,-1.01,;83.33,-1.78,;84.66,-1.01,;84.66,.53,;83.32,1.3,;81.99,.53,;82,-4.09,;82,-5.63,;83.33,-3.32,;84.66,-4.09,;84.66,-5.63,;86,-3.31,;86,-1.77,;87.33,-4.09,;88.67,-3.32,;88.67,-1.78,;90,-1,;91.4,-1.62,;92.43,-.47,;91.66,.85,;92.14,2.32,;91.11,3.46,;89.6,3.14,;89.13,1.67,;90.16,.53,;90,-4.08,;90,-5.62,;91.33,-3.31,;92.67,-4.08,;92.67,-5.62,;94,-6.38,;94,-7.92,;95.34,-5.62,;94,-3.3,;94,-1.76,;95.33,-4.08,;96.67,-3.31,;96.67,-1.76,;98,-.99,;95.33,-.99,;98,-4.07,;98,-5.61,;99.34,-3.3,;100.67,-4.07,;100.67,-5.61,;102,-6.38,;102,-7.91,;103.34,-8.68,;103.34,-10.22,;102,-3.3,;102,-1.76,;103.34,-4.06,;104.67,-3.29,;106,-4.07,;106,-5.6,;107.34,-3.29,;108.67,-4.06,;108.67,-5.6,;110.01,-6.37,;110.01,-7.91,;111.35,-8.68,;111.35,-10.21,;110.01,-10.98,;112.68,-10.98,;110.01,-3.29,;111.34,-4.05,;110.01,-1.74,)|
Show InChI InChI=1S/C154H236N42O45/c1-17-80(10)124(151(239)187-106(61-87-33-20-18-21-34-87)139(227)173-83(13)130(218)182-109(64-90-67-166-95-38-25-24-37-93(90)95)142(230)184-105(60-77(4)5)143(231)193-122(78(6)7)149(237)181-98(39-26-29-55-155)133(221)167-69-116(206)174-96(127(160)215)42-32-58-165-154(161)162)195-138(226)103(50-54-120(211)212)180-136(224)99(40-27-30-56-156)179-137(225)102(48-52-115(159)205)177-129(217)82(12)172-135(223)101(47-51-114(158)204)175-117(207)70-168-132(220)97(41-28-31-57-164-86(16)202)178-140(228)104(59-76(2)3)183-141(229)107(63-89-43-45-92(203)46-44-89)185-146(234)111(72-197)189-148(236)113(74-199)190-150(238)123(79(8)9)194-145(233)110(66-121(213)214)186-147(235)112(73-198)191-153(241)126(85(15)201)196-144(232)108(62-88-35-22-19-23-36-88)188-152(240)125(84(14)200)192-118(208)71-169-134(222)100(49-53-119(209)210)176-128(216)81(11)171-131(219)94(157)65-91-68-163-75-170-91/h18-25,33-38,43-46,67-68,75-85,94,96-113,122-126,166,197-201,203H,17,26-32,39-42,47-66,69-74,155-157H2,1-16H3,(H2,158,204)(H2,159,205)(H2,160,215)(H,163,170)(H,164,202)(H,167,221)(H,168,220)(H,169,222)(H,171,219)(H,172,223)(H,173,227)(H,174,206)(H,175,207)(H,176,216)(H,177,217)(H,178,228)(H,179,225)(H,180,224)(H,181,237)(H,182,218)(H,183,229)(H,184,230)(H,185,234)(H,186,235)(H,187,239)(H,188,240)(H,189,236)(H,190,238)(H,191,241)(H,192,208)(H,193,231)(H,194,233)(H,195,226)(H,196,232)(H,209,210)(H,211,212)(H,213,214)(H4,161,162,165)/t80-,81-,82-,83-,84+,85+,94-,96-,97-,98-,99-,100-,101-,102-,103-,104-,105-,106-,107-,108-,109-,110-,111-,112-,113-,122-,123-,124-,125-,126-/m0/s1
PDB

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
KEGG
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.60E+3n/an/an/an/an/an/a



University of Texas at Dallas

Curated by ChEMBL


Assay Description
Displacement of [125I]exendin(9-39) from human GLP1R expressed in HEK293 cells


Bioorg Med Chem 16: 10106-12 (2008)


Article DOI: 10.1016/j.bmc.2008.10.006
BindingDB Entry DOI: 10.7270/Q2B857ZT
More data for this
Ligand-Target Pair