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BDBM50045509 CHEMBL3314226

SMILES: CNC(=N)NCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)NNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)C1CC1)[C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O

InChI Key: InChIKey=ROUIGZVDXBTXSV-DMVZKCHWNA-N

Data: 2 KI  2 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 4 hits for monomerid = 50045509   
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
G-protein Coupled Receptor 54


(Homo sapiens (human))
BDBM50045509
PNG
(CHEMBL3314226)
Show SMILES CNC(=N)NCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)NNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)C1CC1)[C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O
Show InChI InChI=1/C66H85N17O13/c1-35(2)27-49(59(90)74-47(19-12-26-71-65(69)70-4)58(89)75-48(56(68)87)30-40-33-72-45-17-10-8-15-43(40)45)80-66(96)83-82-63(94)51(28-37-13-6-5-7-14-37)79-64(95)55(36(3)84)81-62(93)53(32-54(67)86)78-61(92)52(31-41-34-73-46-18-11-9-16-44(41)46)77-60(91)50(76-57(88)39-22-23-39)29-38-20-24-42(85)25-21-38/h5-11,13-18,20-21,24-25,33-36,39,47-53,55,72-73,84-85H,12,19,22-23,26-32H2,1-4H3,(H2,67,86)(H2,68,87)(H,74,90)(H,75,89)(H,76,88)(H,77,91)(H,78,92)(H,79,95)(H,81,93)(H,82,94)(H3,69,70,71)(H2,80,83,96)/t36-,47+,48+,49+,50-,51+,52-,53+,55+/s2
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Article
PubMed
0.0340n/an/an/an/an/an/an/an/a



Takeda Pharmaceutical Company Ltd.

Curated by ChEMBL


Assay Description
Displacement of radioligand from human KISS1R transfected in CHO cells


J Med Chem 57: 6105-15 (2014)

More data for this
Ligand-Target Pair
KiSS-1 receptor


(Rattus norvegicus)
BDBM50045509
PNG
(CHEMBL3314226)
Show SMILES CNC(=N)NCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)NNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)C1CC1)[C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O
Show InChI InChI=1/C66H85N17O13/c1-35(2)27-49(59(90)74-47(19-12-26-71-65(69)70-4)58(89)75-48(56(68)87)30-40-33-72-45-17-10-8-15-43(40)45)80-66(96)83-82-63(94)51(28-37-13-6-5-7-14-37)79-64(95)55(36(3)84)81-62(93)53(32-54(67)86)78-61(92)52(31-41-34-73-46-18-11-9-16-44(41)46)77-60(91)50(76-57(88)39-22-23-39)29-38-20-24-42(85)25-21-38/h5-11,13-18,20-21,24-25,33-36,39,47-53,55,72-73,84-85H,12,19,22-23,26-32H2,1-4H3,(H2,67,86)(H2,68,87)(H,74,90)(H,75,89)(H,76,88)(H,77,91)(H,78,92)(H,79,95)(H,81,93)(H,82,94)(H3,69,70,71)(H2,80,83,96)/t36-,47+,48+,49+,50-,51+,52-,53+,55+/s2
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Article
PubMed
0.0870n/an/an/an/an/an/an/an/a



Takeda Pharmaceutical Company Ltd.

Curated by ChEMBL


Assay Description
Displacement of radioligand from rat KISS1R transfected in CHO cells


J Med Chem 57: 6105-15 (2014)

More data for this
Ligand-Target Pair
G-protein Coupled Receptor 54


(Homo sapiens (human))
BDBM50045509
PNG
(CHEMBL3314226)
Show SMILES CNC(=N)NCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)NNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)C1CC1)[C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O
Show InChI InChI=1/C66H85N17O13/c1-35(2)27-49(59(90)74-47(19-12-26-71-65(69)70-4)58(89)75-48(56(68)87)30-40-33-72-45-17-10-8-15-43(40)45)80-66(96)83-82-63(94)51(28-37-13-6-5-7-14-37)79-64(95)55(36(3)84)81-62(93)53(32-54(67)86)78-61(92)52(31-41-34-73-46-18-11-9-16-44(41)46)77-60(91)50(76-57(88)39-22-23-39)29-38-20-24-42(85)25-21-38/h5-11,13-18,20-21,24-25,33-36,39,47-53,55,72-73,84-85H,12,19,22-23,26-32H2,1-4H3,(H2,67,86)(H2,68,87)(H,74,90)(H,75,89)(H,76,88)(H,77,91)(H,78,92)(H,79,95)(H,81,93)(H,82,94)(H3,69,70,71)(H2,80,83,96)/t36-,47+,48+,49+,50-,51+,52-,53+,55+/s2
Reactome pathway
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antibodypedia
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Article
PubMed
n/an/an/an/a 0.820n/an/an/an/a



Takeda Pharmaceutical Company Ltd.

Curated by ChEMBL


Assay Description
Agonist activity at human KISS1R transfected in CHO cells assessed as intracellular calcium flux after 24 hrs by functional FLIPR assay


J Med Chem 57: 6105-15 (2014)

More data for this
Ligand-Target Pair
KiSS-1 receptor


(Rattus norvegicus)
BDBM50045509
PNG
(CHEMBL3314226)
Show SMILES CNC(=N)NCCC[C@H](NC(=O)[C@H](CC(C)C)NC(=O)NNC(=O)[C@H](Cc1ccccc1)NC(=O)[C@@H](NC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](Cc1c[nH]c2ccccc12)NC(=O)[C@@H](Cc1ccc(O)cc1)NC(=O)C1CC1)[C@@H](C)O)C(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(N)=O
Show InChI InChI=1/C66H85N17O13/c1-35(2)27-49(59(90)74-47(19-12-26-71-65(69)70-4)58(89)75-48(56(68)87)30-40-33-72-45-17-10-8-15-43(40)45)80-66(96)83-82-63(94)51(28-37-13-6-5-7-14-37)79-64(95)55(36(3)84)81-62(93)53(32-54(67)86)78-61(92)52(31-41-34-73-46-18-11-9-16-44(41)46)77-60(91)50(76-57(88)39-22-23-39)29-38-20-24-42(85)25-21-38/h5-11,13-18,20-21,24-25,33-36,39,47-53,55,72-73,84-85H,12,19,22-23,26-32H2,1-4H3,(H2,67,86)(H2,68,87)(H,74,90)(H,75,89)(H,76,88)(H,77,91)(H,78,92)(H,79,95)(H,81,93)(H,82,94)(H3,69,70,71)(H2,80,83,96)/t36-,47+,48+,49+,50-,51+,52-,53+,55+/s2
Reactome pathway
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Article
PubMed
n/an/an/an/a 4.20n/an/an/an/a



Takeda Pharmaceutical Company Ltd.

Curated by ChEMBL


Assay Description
Agonist activity at rat KISS1R transfected in CHO cells assessed as intracellular calcium flux after 24 hrs by functional FLIPR assay


J Med Chem 57: 6105-15 (2014)

More data for this
Ligand-Target Pair