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BDBM50099174 4-Chloro-N-[(R)-2-(1H-indol-3-yl)-1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-benzamidine::CHEMBL362859

SMILES: NC(=N[C@H](Cc1c[nH]c2ccccc12)c1nc(c[nH]1)-c1ccccc1)c1ccc(Cl)cc1

InChI Key: InChIKey=UEBYNWAHMKBMAT-HSZRJFAPSA-N

Data: 5 KI

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 5 hits for monomerid = 50099174   
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
Somatostatin receptor type 3


(Homo sapiens (Human))
BDBM50099174
PNG
(4-Chloro-N-[(R)-2-(1H-indol-3-yl)-1-(4-phenyl-1H-i...)
Show SMILES NC(=N[C@H](Cc1c[nH]c2ccccc12)c1nc(c[nH]1)-c1ccccc1)c1ccc(Cl)cc1 |w:1.0|
Show InChI InChI=1S/C26H22ClN5/c27-20-12-10-18(11-13-20)25(28)31-23(14-19-15-29-22-9-5-4-8-21(19)22)26-30-16-24(32-26)17-6-2-1-3-7-17/h1-13,15-16,23,29H,14H2,(H2,28,31)(H,30,32)/t23-/m1/s1
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PC cid
PC sid
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PubMed
79n/an/an/an/an/an/an/an/a



Institut Henri Beaufour

Curated by ChEMBL


Assay Description
Inhibition of human sst3 receptor expressed in CHO cells


Bioorg Med Chem Lett 11: 991-5 (2001)


BindingDB Entry DOI: 10.7270/Q2D50NHN
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50099174
PNG
(4-Chloro-N-[(R)-2-(1H-indol-3-yl)-1-(4-phenyl-1H-i...)
Show SMILES NC(=N[C@H](Cc1c[nH]c2ccccc12)c1nc(c[nH]1)-c1ccccc1)c1ccc(Cl)cc1 |w:1.0|
Show InChI InChI=1S/C26H22ClN5/c27-20-12-10-18(11-13-20)25(28)31-23(14-19-15-29-22-9-5-4-8-21(19)22)26-30-16-24(32-26)17-6-2-1-3-7-17/h1-13,15-16,23,29H,14H2,(H2,28,31)(H,30,32)/t23-/m1/s1
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PubMed
691n/an/an/an/an/an/an/an/a



Institut Henri Beaufour

Curated by ChEMBL


Assay Description
Inhibition of human sst5 receptor expressed in CHO cells


Bioorg Med Chem Lett 11: 991-5 (2001)


BindingDB Entry DOI: 10.7270/Q2D50NHN
More data for this
Ligand-Target Pair
Somatostatin receptor type 1


(Homo sapiens (Human))
BDBM50099174
PNG
(4-Chloro-N-[(R)-2-(1H-indol-3-yl)-1-(4-phenyl-1H-i...)
Show SMILES NC(=N[C@H](Cc1c[nH]c2ccccc12)c1nc(c[nH]1)-c1ccccc1)c1ccc(Cl)cc1 |w:1.0|
Show InChI InChI=1S/C26H22ClN5/c27-20-12-10-18(11-13-20)25(28)31-23(14-19-15-29-22-9-5-4-8-21(19)22)26-30-16-24(32-26)17-6-2-1-3-7-17/h1-13,15-16,23,29H,14H2,(H2,28,31)(H,30,32)/t23-/m1/s1
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PubMed
1.73E+3n/an/an/an/an/an/an/an/a



Institut Henri Beaufour

Curated by ChEMBL


Assay Description
Inhibition of human sst1 receptor expressed in CHO cells


Bioorg Med Chem Lett 11: 991-5 (2001)


BindingDB Entry DOI: 10.7270/Q2D50NHN
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50099174
PNG
(4-Chloro-N-[(R)-2-(1H-indol-3-yl)-1-(4-phenyl-1H-i...)
Show SMILES NC(=N[C@H](Cc1c[nH]c2ccccc12)c1nc(c[nH]1)-c1ccccc1)c1ccc(Cl)cc1 |w:1.0|
Show InChI InChI=1S/C26H22ClN5/c27-20-12-10-18(11-13-20)25(28)31-23(14-19-15-29-22-9-5-4-8-21(19)22)26-30-16-24(32-26)17-6-2-1-3-7-17/h1-13,15-16,23,29H,14H2,(H2,28,31)(H,30,32)/t23-/m1/s1
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3.47E+3n/an/an/an/an/an/an/an/a



Institut Henri Beaufour

Curated by ChEMBL


Assay Description
Inhibition of human sst2 receptor expressed in CHO cells


Bioorg Med Chem Lett 11: 991-5 (2001)


BindingDB Entry DOI: 10.7270/Q2D50NHN
More data for this
Ligand-Target Pair
Somatostatin receptor type 4


(Homo sapiens (Human))
BDBM50099174
PNG
(4-Chloro-N-[(R)-2-(1H-indol-3-yl)-1-(4-phenyl-1H-i...)
Show SMILES NC(=N[C@H](Cc1c[nH]c2ccccc12)c1nc(c[nH]1)-c1ccccc1)c1ccc(Cl)cc1 |w:1.0|
Show InChI InChI=1S/C26H22ClN5/c27-20-12-10-18(11-13-20)25(28)31-23(14-19-15-29-22-9-5-4-8-21(19)22)26-30-16-24(32-26)17-6-2-1-3-7-17/h1-13,15-16,23,29H,14H2,(H2,28,31)(H,30,32)/t23-/m1/s1
KEGG

UniProtKB/SwissProt

antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

PubMed
3.84E+3n/an/an/an/an/an/an/an/a



Institut Henri Beaufour

Curated by ChEMBL


Assay Description
Inhibition of human sst4 receptor expressed in CHO cells


Bioorg Med Chem Lett 11: 991-5 (2001)


BindingDB Entry DOI: 10.7270/Q2D50NHN
More data for this
Ligand-Target Pair