MITOTENAMINE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C13H15BrClNS
Molecular Weight	332.687
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of MITOTENAMINE

Structure Search

SMILES

CCN(CCCl)CC1=CSC2=C1C=C(Br)C=C2

InChI

InChIKey=SZLHBBCRNVPTRZ-UHFFFAOYSA-N

InChI=1S/C13H15BrClNS/c1-2-16(6-5-15)8-10-9-17-13-4-3-11(14)7-12(10)13/h3-4,7,9H,2,5-6,8H2,1H3

HIDE SMILES / InChI

Molecular Formula	C13H15BrClNS
Molecular Weight	332.687
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Description
Sources: https://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&ND=3&adjacent=true&locale=en_EP&FT=D&date=20050831&CC=CN&NR=1660436A&KC=A | https://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&ND=3&adjacent=true&locale=en_EP&FT=D&date=20051012&CC=CN&NR=1679950A&KC=A | https://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&ND=3&adjacent=true&locale=en_EP&FT=D&date=20051012&CC=CN&NR=1679950A&KC=A

Mitotenamine is benzo[b]thiophene derivative with nucleotoxic activity patented by Shandong Lanjin Biotech Co. for cancer chemotherapy.

Originator

Approval Year

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:26:03 GMT 2025` Edited by `admin` on `Mon Mar 31 18:26:03 GMT 2025`
Record UNII	2879S26V4P
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

mitotenamine [INN]

Preferred Name

English

MITOTENAMINE

Official Name

English

5-BROMO-N-(2-CHLOROETHYL)-N-ETHYLBENZO(B)THIOPHENE-3-METHYLAMINE

Systematic Name

English

Classification Tree Code System Code

NCI_THESAURUS

C1590

Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025

Code System Code Type Description

ChEMBL

CHEMBL2104935

Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025

PRIMARY

EPA CompTox

DTXSID10227741

Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025

PRIMARY

FDA UNII

2879S26V4P

Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025

PRIMARY

PUBCHEM

23793

Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025

PRIMARY

CAS

7696-00-6

Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025

PRIMARY

SMS_ID

100000080900

Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025

PRIMARY

EVMPD

SUB09011MIG

Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025

PRIMARY

INN

2304

Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025

PRIMARY

NCI_THESAURUS

C66167

Created by admin on Mon Mar 31 18:26:03 GMT 2025 , Edited by admin on Mon Mar 31 18:26:03 GMT 2025

PRIMARY

Related Record Type Details


					2879S26V4P

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