BROMADOLINE

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C15H21BrN2O
Molecular Weight	325.244
Optical Activity	( + / - )
Defined Stereocenters	2 / 2
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of BROMADOLINE

Structure Search

SMILES

CN(C)[C@H]1CCCC[C@@H]1NC(=O)C2=CC=C(Br)C=C2

InChI

InChIKey=UFDJFJYMMIZKLG-KBPBESRZSA-N

InChI=1S/C15H21BrN2O/c1-18(2)14-6-4-3-5-13(14)17-15(19)11-7-9-12(16)10-8-11/h7-10,13-14H,3-6H2,1-2H3,(H,17,19)/t13-,14-/m0/s1

HIDE SMILES / InChI

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4009438 | https://www.ncbi.nlm.nih.gov/pubmed/3559988 | https://worldwide.espacenet.com/publicationDetails/biblio?DB=EPODOC&II=0&ND=3&adjacent=true&locale=en_EP&FT=D&date=19780518&CC=DE&NR=2749984A1&KC=A1

Bromadoline is a selective agonist of a μ-opioid receptor with potent analgesic activity developed by the Upjohn company in the 1970s for pain management.

CNS Activity

Originator

Approval Year

PubMed

PubMed

Title	Date	PubMed
Evaluation of the receptor selectivities of opioid drugs by investigating the block of their effect on urine output by beta-funaltrexamine.	1987-03	3559988

Patents

Patents

Name

Type

Language

BROMADOLINE

Official Name

English

BENZAMIDE, 4-BROMO-N-(2-(DIMETHYLAMINO)CYCLOHEXYL)-, TRANS-

Preferred Name

English

U-47931E

Common Name

English

trans-4-bromo-N-2-(dimethylamino)cyclohexyl]-benzamide

Common Name

English

TRANS-P-BROMO-N-(2-(DIMETHYLAMINO)CYCLOHEXYL)BENZAMIDE

Common Name

English

Bromadoline [WHO-DD]

Common Name

English

bromadoline [INN]

Common Name

English

Classification Tree Code System Code

WIKIPEDIA

Designer-drugs-Bromadoline

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

NCI_THESAURUS

C241

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

Code System Code Type Description

EPA CompTox

DTXSID40217897

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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EVMPD

SUB05905MIG

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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WIKIPEDIA

BROMADOLINE

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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NCI_THESAURUS

C79931

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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MESH

C045811

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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ChEMBL

CHEMBL2110893

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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CAS

67579-24-2

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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CAYMAN

20530

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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SMS_ID

100000088652

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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PUBCHEM

54753

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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FDA UNII

R8DWN01P1M

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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INN

5355

Created by admin on Wed Apr 02 07:52:35 GMT 2025 , Edited by admin on Wed Apr 02 07:52:35 GMT 2025

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ACTIVE MOIETY


					R8DWN01P1M

SALT/SOLVATE (PARENT)


					0NLD148UB3

BROMADOLINE MALEATE