BindingDB logo
myBDB logout

BDBM50175595 (4-amino-3-iodo)-D-Phe-c[Cys-(3-iodo)-Tyr-D-Trp-Lys-Val-Cys]-Asp-NH2::CHEMBL410110

SMILES: CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)c(I)c2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](CC(O)=O)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(N)c(I)c1

InChI Key: InChIKey=KCLKKUARHZJXBX-ADLHATSZSA-N

Data: 3 IC50

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 = 50175595   
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))
BDBM50175595
PNG
((4-amino-3-iodo)-D-Phe-c[Cys-(3-iodo)-Tyr-D-Trp-Ly...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)c(I)c2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](CC(O)=O)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(N)c(I)c1
Show InChI InChI=1S/C50H64I2N12O11S2/c1-24(2)42-50(75)63-39(48(73)59-35(43(56)68)20-41(66)67)23-77-76-22-38(62-44(69)32(55)17-25-10-12-31(54)29(51)15-25)49(74)60-36(18-26-11-13-40(65)30(52)16-26)46(71)61-37(19-27-21-57-33-8-4-3-7-28(27)33)47(72)58-34(45(70)64-42)9-5-6-14-53/h3-4,7-8,10-13,15-16,21,24,32,34-39,42,57,65H,5-6,9,14,17-20,22-23,53-55H2,1-2H3,(H2,56,68)(H,58,72)(H,59,73)(H,60,74)(H,61,71)(H,62,69)(H,63,75)(H,64,70)(H,66,67)/t32-,34-,35-,36-,37+,38-,39+,42+/m0/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+3n/an/an/an/an/an/a



University of California-San Diego

Curated by ChEMBL


Assay Description
Inhibitory concentration against human somatostatin receptor type 3 in CHO-K1 cells


J Med Chem 48: 6643-52 (2005)


Article DOI: 10.1021/jm050376t
BindingDB Entry DOI: 10.7270/Q2D50NRS
More data for this
Ligand-Target Pair
Somatostatin receptor type 5


(Homo sapiens (Human))
BDBM50175595
PNG
((4-amino-3-iodo)-D-Phe-c[Cys-(3-iodo)-Tyr-D-Trp-Ly...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)c(I)c2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](CC(O)=O)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(N)c(I)c1
Show InChI InChI=1S/C50H64I2N12O11S2/c1-24(2)42-50(75)63-39(48(73)59-35(43(56)68)20-41(66)67)23-77-76-22-38(62-44(69)32(55)17-25-10-12-31(54)29(51)15-25)49(74)60-36(18-26-11-13-40(65)30(52)16-26)46(71)61-37(19-27-21-57-33-8-4-3-7-28(27)33)47(72)58-34(45(70)64-42)9-5-6-14-53/h3-4,7-8,10-13,15-16,21,24,32,34-39,42,57,65H,5-6,9,14,17-20,22-23,53-55H2,1-2H3,(H2,56,68)(H,58,72)(H,59,73)(H,60,74)(H,61,71)(H,62,69)(H,63,75)(H,64,70)(H,66,67)/t32-,34-,35-,36-,37+,38-,39+,42+/m0/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 2.90n/an/an/an/an/an/a



University of California-San Diego

Curated by ChEMBL


Assay Description
Inhibitory concentration against human somatostatin receptor type 5 in CHO-K1 cells


J Med Chem 48: 6643-52 (2005)


Article DOI: 10.1021/jm050376t
BindingDB Entry DOI: 10.7270/Q2D50NRS
More data for this
Ligand-Target Pair
Somatostatin receptor type 2


(Homo sapiens (Human))
BDBM50175595
PNG
((4-amino-3-iodo)-D-Phe-c[Cys-(3-iodo)-Tyr-D-Trp-Ly...)
Show SMILES CC(C)[C@H]1NC(=O)[C@H](CCCCN)NC(=O)[C@@H](Cc2c[nH]c3ccccc23)NC(=O)[C@H](Cc2ccc(O)c(I)c2)NC(=O)[C@H](CSSC[C@@H](NC1=O)C(=O)N[C@@H](CC(O)=O)C(N)=O)NC(=O)[C@@H](N)Cc1ccc(N)c(I)c1
Show InChI InChI=1S/C50H64I2N12O11S2/c1-24(2)42-50(75)63-39(48(73)59-35(43(56)68)20-41(66)67)23-77-76-22-38(62-44(69)32(55)17-25-10-12-31(54)29(51)15-25)49(74)60-36(18-26-11-13-40(65)30(52)16-26)46(71)61-37(19-27-21-57-33-8-4-3-7-28(27)33)47(72)58-34(45(70)64-42)9-5-6-14-53/h3-4,7-8,10-13,15-16,21,24,32,34-39,42,57,65H,5-6,9,14,17-20,22-23,53-55H2,1-2H3,(H2,56,68)(H,58,72)(H,59,73)(H,60,74)(H,61,71)(H,62,69)(H,63,75)(H,64,70)(H,66,67)/t32-,34-,35-,36-,37+,38-,39+,42+/m0/s1
PDB

KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.90n/an/an/an/an/an/a



University of California-San Diego

Curated by ChEMBL


Assay Description
Inhibitory concentration against human somatostatin receptor type 2 in CC531 cells


J Med Chem 48: 6643-52 (2005)


Article DOI: 10.1021/jm050376t
BindingDB Entry DOI: 10.7270/Q2D50NRS
More data for this
Ligand-Target Pair