INDOPINE HYDROCHLORIDE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C23H28N2.ClH
Molecular Weight	368.943
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of INDOPINE HYDROCHLORIDE

Structure Search

SMILES

Cl.C(CC1=CNC2=C1C=CC=C2)C3CCN(CCC4=CC=CC=C4)CC3

InChI

InChIKey=HMVPYHOOYHEFEZ-UHFFFAOYSA-N

InChI=1S/C23H28N2.ClH/c1-2-6-19(7-3-1)12-15-25-16-13-20(14-17-25)10-11-21-18-24-23-9-5-4-8-22(21)23;/h1-9,18,20,24H,10-17H2;1H

HIDE SMILES / InChI

Molecular Formula	ClH
Molecular Weight	36.461
Charge	0
Count

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

Molecular Formula	C23H28N2
Molecular Weight	332.4818
Charge	0
Count

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

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/15921464 | https://pubs.acs.org/doi/abs/10.1021/jo01067a084
Curator's Comment: FRM1693

Indopine is indolylalkyl derivative patented by Irwin, Neisler and Co as potent analgesic.

Originator

Approval Year

PubMed

PubMed

Title	Date	PubMed
Classification of substrates and inhibitors of P-glycoprotein using unsupervised machine learning approach.	2005-06-01	15921464

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:19:31 GMT 2025` Edited by `admin` on `Mon Mar 31 18:19:31 GMT 2025`
Record UNII	CZ5QG07777
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

INDOPINE HYDROCHLORIDE

Common Name

English

NSC-84972

Preferred Name

English

INDOPINE HCL

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C257

Created by admin on Mon Mar 31 18:19:31 GMT 2025 , Edited by admin on Mon Mar 31 18:19:31 GMT 2025

Code System Code Type Description

PUBCHEM

216378

Created by admin on Mon Mar 31 18:19:31 GMT 2025 , Edited by admin on Mon Mar 31 18:19:31 GMT 2025

PRIMARY

CAS

24361-13-5

Created by admin on Mon Mar 31 18:19:31 GMT 2025 , Edited by admin on Mon Mar 31 18:19:31 GMT 2025

PRIMARY

EPA CompTox

DTXSID80179107

Created by admin on Mon Mar 31 18:19:31 GMT 2025 , Edited by admin on Mon Mar 31 18:19:31 GMT 2025

PRIMARY

FDA UNII

CZ5QG07777

Created by admin on Mon Mar 31 18:19:31 GMT 2025 , Edited by admin on Mon Mar 31 18:19:31 GMT 2025

PRIMARY

NSC

84972

Created by admin on Mon Mar 31 18:19:31 GMT 2025 , Edited by admin on Mon Mar 31 18:19:31 GMT 2025

PRIMARY

NCI_THESAURUS

C77359

Created by admin on Mon Mar 31 18:19:31 GMT 2025 , Edited by admin on Mon Mar 31 18:19:31 GMT 2025

PRIMARY

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