BROMOCRIPTINE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C32H40BrN5O5
Molecular Weight	654.594
Optical Activity	UNSPECIFIED
Defined Stereocenters	6 / 6
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of BROMOCRIPTINE

Structure Search

SMILES

[H][C@@]12CCCN1C(=O)[C@H](CC(C)C)N3C(=O)[C@](NC(=O)[C@H]4CN(C)[C@]5([H])CC6=C(Br)NC7=C6C(=CC=C7)C5=C4)(O[C@@]23O)C(C)C

InChI

InChIKey=OZVBMTJYIDMWIL-AYFBDAFISA-N

InChI=1S/C32H40BrN5O5/c1-16(2)12-24-29(40)37-11-7-10-25(37)32(42)38(24)30(41)31(43-32,17(3)4)35-28(39)18-13-20-19-8-6-9-22-26(19)21(27(33)34-22)14-23(20)36(5)15-18/h6,8-9,13,16-18,23-25,34,42H,7,10-12,14-15H2,1-5H3,(H,35,39)/t18-,23-,24+,25+,31-,32+/m1/s1

HIDE SMILES / InChI

Molecular Formula	C32H40BrN5O5
Molecular Weight	654.594
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	6 / 6
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 17:06:16 UTC 2023` Edited by `admin` on `Sat Dec 16 17:06:16 UTC 2023`
Record UNII	3A64E3G5ZO
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

BROMOCRIPTINE

Official Name

English

SANDOZ 15-754

Code

English

2-Bromo-α-ergocryptine

Common Name

English

BROMOCRIPTINE [USAN]

Common Name

English

ERGOTAMAN-3',6',18-TRIONE, 2-BROMO-12'-HYDROXY-2'-(1-METHYLETHYL)-5'-(2-METHYLPROPYL)-, (5'.ALPHA.)-

Common Name

English

ERGOCRYPTINE, 2-BROMO-

Common Name

English

Bromocriptine [WHO-DD]

Common Name

English

BROMOCRIPTINE [MI]

Common Name

English

BROMOCRIPTINE [VANDF]

Common Name

English

bromocriptine [INN]

Common Name

English

(+)-BROMOCRIPTINE

Systematic Name

English

BROMERGOCRYPTINE

Common Name

English

Classification Tree Code System Code

LIVERTOX

NBK548601

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

NDF-RT

N0000175827

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

WHO-ATC

N04BC01

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

NDF-RT

N0000007618

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

NDF-RT

N0000007618

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

NCI_THESAURUS

C1509

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

WHO-ATC

G02CB01

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

WHO-VATC

QG02CB01

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

NCI_THESAURUS

C66884

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

Code System Code Type Description

MESH

D001971

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

CHEBI

3181

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

EPA CompTox

DTXSID1022687

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

IUPHAR

35

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

FDA UNII

3A64E3G5ZO

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

PUBCHEM

31101

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

SMS_ID

100000088678

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

ECHA (EC/EINECS)

247-128-5

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

NCI_THESAURUS

C62010

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

EVMPD

SUB05918MIG

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

RXCUI

1760

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

RxNorm

WIKIPEDIA

BROMOCRIPTINE

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

INN

3365

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

CAS

25614-03-3

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

ChEMBL

CHEMBL493

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

DRUG BANK

DB01200

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

MERCK INDEX

m2694

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

Merck Index

LACTMED

Bromocriptine

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

DAILYMED

3A64E3G5ZO

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

DRUG CENTRAL

403

Created by admin on Sat Dec 16 17:06:17 UTC 2023 , Edited by admin on Sat Dec 16 17:06:17 UTC 2023

PRIMARY

Related Record Type Details


					6D53G0FD0Z

PLASMA PROTEIN FRACTION (HUMAN)

BINDER->LIGAND

Interaction Type:

BINDING

Amount:


					19GBD6T9L7

D(2) DOPAMINE RECEPTOR

TARGET -> AGONIST

Amount:


					G9XQ9S7T2F

D(3) DOPAMINE RECEPTOR

TARGET -> AGONIST


					FFP983J3OD

BROMOCRIPTINE MESYLATE

SALT/SOLVATE -> PARENT

Related Record Type Details


					3A64E3G5ZO

ACTIVE MOIETY

Name	Property Type	Amount	Referenced Substance	Defining	Parameters	References
Volume of Distribution	PHARMACOKINETIC

Biological Half-life	PHARMACOKINETIC