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Details

Stereochemistry ABSOLUTE
Molecular Formula C76H104N18O19S2
Molecular Weight 1637.878
Optical Activity UNSPECIFIED
Defined Stereocenters 15 / 15
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SOMATOSTATIN

SMILES

[H][C@]1(NC(=O)[C@H](CCCCN)NC(=O)[C@H](CC2=CNC3=C2C=CC=C3)NC(=O)[C@H](CC4=CC=CC=C4)NC(=O)[C@H](CC5=CC=CC=C5)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CSSC[C@H](NC(=O)[C@H](CO)NC(=O)[C@@]([H])(NC(=O)[C@H](CC6=CC=CC=C6)NC1=O)[C@@H](C)O)C(O)=O)NC(=O)CNC(=O)[C@H](C)N)[C@@H](C)O

InChI

InChIKey=NHXLMOGPVYXJNR-ATOGVRKGSA-N
InChI=1S/C76H104N18O19S2/c1-41(79)64(100)82-37-61(99)83-58-39-114-115-40-59(76(112)113)92-72(108)57(38-95)91-75(111)63(43(3)97)94-71(107)54(33-46-23-11-6-12-24-46)90-74(110)62(42(2)96)93-66(102)51(28-16-18-30-78)84-69(105)55(34-47-36-81-49-26-14-13-25-48(47)49)88-68(104)53(32-45-21-9-5-10-22-45)86-67(103)52(31-44-19-7-4-8-20-44)87-70(106)56(35-60(80)98)89-65(101)50(85-73(58)109)27-15-17-29-77/h4-14,19-26,36,41-43,50-59,62-63,81,95-97H,15-18,27-35,37-40,77-79H2,1-3H3,(H2,80,98)(H,82,100)(H,83,99)(H,84,105)(H,85,109)(H,86,103)(H,87,106)(H,88,104)(H,89,101)(H,90,110)(H,91,111)(H,92,108)(H,93,102)(H,94,107)(H,112,113)/t41-,42+,43+,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-,62-,63-/m0/s1

HIDE SMILES / InChI

Molecular Formula C76H104N18O19S2
Molecular Weight 1637.878
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 15 / 15
E/Z Centers 2
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 19:47:46 UTC 2023
Edited
by admin
on Sat Dec 16 19:47:46 UTC 2023
Record UNII
6E20216Q0L
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SOMATOSTATIN
EP   INN   MART.   MI   WHO-DD  
INN  
Official Name English
SOMATOSTATIN [MART.]
Common Name English
SRIF-14
Code English
SOMATOSTATIN-14
Common Name English
Somatostatin [WHO-DD]
Common Name English
SOMATOSTATIN [MI]
Common Name English
somatostatin [INN]
Common Name English
SOMATOSTATIN [EP MONOGRAPH]
Common Name English
ALA-GLY-CYS-LYS-ASN-PHE-PHE-TRP-LYS-THR-PHE-THR-SER-CYS 3,14-disulfide
Systematic Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 21587
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
FDA ORPHAN DRUG 86094
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
LOINC 2960-3
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
LOINC 49792-5
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
WHO-VATC QH01CB01
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
WHO-ATC H01CB01
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
LOINC 2961-1
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
Code System Code Type Description
FDA UNII
6E20216Q0L
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
CAS
51110-01-1
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
NO STRUCTURE GIVEN
SMS_ID
100000092022
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
DRUG BANK
DB09099
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
DRUG CENTRAL
2997
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
ChEMBL
CHEMBL1823872
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
CAS
38916-34-6
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
EVMPD
SUB12320MIG
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
MERCK INDEX
m10111
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY Merck Index
PUBCHEM
16129706
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
INN
4311
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
CHEBI
64628
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
ECHA (EC/EINECS)
254-186-5
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
EPA CompTox
DTXSID8046793
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
RXCUI
9939
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY RxNorm
ECHA (EC/EINECS)
256-969-7
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
ALTERNATIVE
MESH
D013004
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
NCI_THESAURUS
C836
Created by admin on Sat Dec 16 19:47:48 UTC 2023 , Edited by admin on Sat Dec 16 19:47:48 UTC 2023
PRIMARY
Related Record Type Details
DERIVATIVE -> PARENT
DERIVATIVE -> PARENT
AGONIST -> TARGET
INDUCER -> TARGET
ACTIVATES RELEASE OF SOMATOSTAIN
INGREDIENT -> STARTING MATERIAL
DERIVATIVE -> PARENT
DERIVATIVE -> PARENT
DERIVATIVE -> PARENT
DERIVATIVE -> PARENT
DERIVATIVE -> PARENT
DERIVATIVE -> PARENT
Related Record Type Details
IMPURITY -> PARENT
Related Record Type Details
ACTIVE MOIETY