MetaADEDB 2.0 @ LMMD
Somatostatin
(NHXLMOGPVYXJNR-ATOGVRKGSA-N)
Structure
SMILES
NCCCC[C@@H]1NC(=O)[C@H](CSSC[C@H](NC(=O)[C@H](CO)NC(=O)[C@@H](NC(=O)[C@H](Cc2ccccc2)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@@H](NC1=O)CC(=O)N)Cc1ccccc1)Cc1ccccc1)Cc1c[nH]c2c1cccc2)CCCCN)[C@H](O)C)[C@H](O)C)C(=O)O)NC(=O)CNC(=O)[C@@H](N)C
Type(s)
Approved; Investigational
ATC code(s)
H01CB01
Molecular Formula:
C76H104N18O19S2
Molecular Weight:
1637.880
Log P:
2.2862
Hydrogen Bond Acceptor:
38
Hydrogen Bond Donor:
22
TPSA:
663.83
CAS Number(s):
38916-34-6
Synonym(s)
1.
Somatostatin
2.
Cyclic Somatostatin
3.
Somatostatin-14
4.
Somatotropin Release-Inhibiting Hormone
5.
SRIH-14
6.
Somatofalk
7.
Somatostatin, Cyclic
8.
Somatotropin Release-Inhibiting Factor
9.
Stilamin
10.
Somatostatin 14
11.
Somatotropin Release Inhibiting Factor
12.
Somatotropin Release Inhibiting Hormone
External Link(s)
MeSHD013004
PubChem Compound101826531
16129706
16129681
BindingDB81767
ChEBI64628
CHEMBLCHEMBL1823872
DrugBankDB09099
DrugCentral2997
KEGGdr:D07431
Therapeutic Target DatabaseD0T5RO
Adverse Drug Event(s)
NameNumber of ReportsReference(s)Data Source
1Pain10445233CTD
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