PRENISTEINE

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NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C8H15NO2S
Molecular Weight	189.275
Optical Activity	UNSPECIFIED
Defined Stereocenters	1 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of PRENISTEINE

Structure Search

SMILES

CC(C)=CCSC[C@H](N)C(O)=O

InChI

InChIKey=ULHWZNASVJIOEM-ZETCQYMHSA-N

InChI=1S/C8H15NO2S/c1-6(2)3-4-12-5-7(9)8(10)11/h3,7H,4-5,9H2,1-2H3,(H,10,11)/t7-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C8H15NO2S
Molecular Weight	189.275
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	1 / 1
E/Z Centers	0
Optical Activity	UNSPECIFIED

Description
Sources: https://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&ND=3&adjacent=true&locale=en_EP&FT=D&date=19790401&CC=ES&NR=469060A1&KC=A1

Prenisteine is an enylhomocysteine derivative used as reagent in organic synthesis

Originator

Approval Year

PubMed

PubMed

Title	Date	PubMed
Salirasib inhibits the growth of hepatocarcinoma cell lines in vitro and tumor growth in vivo through ras and mTOR inhibition.	2010-09-22	20860815

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:03:12 GMT 2025` Edited by `admin` on `Mon Mar 31 18:03:12 GMT 2025`
Record UNII	99TA452185
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

PRENISTEINE

Official Name

English

Prenylcysteine

Preferred Name

English

prenisteine [INN]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C74536

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

Code System Code Type Description

CAS

5287-46-7

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

PRIMARY

CHEBI

47914

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

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INN

4716

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

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PUBCHEM

21359

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

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EPA CompTox

DTXSID60200908

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

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EVMPD

SUB10028MIG

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

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SMS_ID

100000081409

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

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ChEMBL

CHEMBL2105861

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

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FDA UNII

99TA452185

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

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NCI_THESAURUS

C73134

Created by admin on Mon Mar 31 18:03:12 GMT 2025 , Edited by admin on Mon Mar 31 18:03:12 GMT 2025

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Related Record Type Details


					99TA452185

ACTIVE MOIETY

Amount: