AMD-3329

Details

Stereochemistry	ACHIRAL
Molecular Formula	C34H50N8.8BrH
Molecular Weight	1218.11
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

Br.Br.Br.Br.Br.Br.Br.Br.C(N1CCNCCC2=CC=CC(CCNCC1)=N2)C3=CC=C(CN4CCNCCC5=CC=CC(CCNCC4)=N5)C=C3

InChI

InChIKey=PTUYNGRETVWEER-UHFFFAOYSA-N

InChI=1S/C34H50N8.8BrH/c1-3-31-11-15-35-19-23-41(24-20-36-16-12-32(4-1)39-31)27-29-7-9-30(10-8-29)28-42-25-21-37-17-13-33-5-2-6-34(40-33)14-18-38-22-26-42;;;;;;;;/h1-10,35-38H,11-28H2;8*1H

HIDE SMILES / InChI

Molecular Formula	C34H50N8
Molecular Weight	570.8144
Charge	0
Count

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

Molecular Formula	BrH
Molecular Weight	80.912
Charge	0
Count

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

Approval Year

PubMed

Title	Date	PubMed
Synthesis and structure-activity relationships of phenylenebis(methylene)-linked bis-azamacrocycles that inhibit HIV-1 and HIV-2 replication by antagonism of the chemokine receptor CXCR4.	1999-09-23	10508445

Substance Class	Chemical Created by `admin` on `Mon Mar 31 22:12:02 GMT 2025` Edited by `admin` on `Mon Mar 31 22:12:02 GMT 2025`
Record UNII	3EUZ070LLN
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

AMD-3329

Common Name

English

4,7,10,17-TETRAAZABICYCLO(11.3.1)HEPTADECA-1(17),13,15-TRIENE, 7,7'-(1,4-PHENYLENEBIS(METHYLENE))BIS-, OCTAHYDROBROMIDE

Preferred Name

English

Code System Code Type Description

PUBCHEM

10725033

Created by admin on Mon Mar 31 22:12:02 GMT 2025 , Edited by admin on Mon Mar 31 22:12:02 GMT 2025

PRIMARY

EPA CompTox

DTXSID20168959

Created by admin on Mon Mar 31 22:12:02 GMT 2025 , Edited by admin on Mon Mar 31 22:12:02 GMT 2025

PRIMARY

FDA UNII

3EUZ070LLN

Created by admin on Mon Mar 31 22:12:02 GMT 2025 , Edited by admin on Mon Mar 31 22:12:02 GMT 2025

PRIMARY

CAS

170861-77-5

Created by admin on Mon Mar 31 22:12:02 GMT 2025 , Edited by admin on Mon Mar 31 22:12:02 GMT 2025

PRIMARY

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