RACEPINEPHRINE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C9H13NO3
Molecular Weight	183.2044
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of RACEPINEPHRINE

Structure Search

SMILES

CNCC(O)C1=CC(O)=C(O)C=C1

InChI

InChIKey=UCTWMZQNUQWSLP-UHFFFAOYSA-N

InChI=1S/C9H13NO3/c1-10-5-9(13)6-2-3-7(11)8(12)4-6/h2-4,9-13H,5H2,1H3

HIDE SMILES / InChI

Molecular Formula	C9H13NO3
Molecular Weight	183.2044
Charge	0
Count

Stereochemistry	RACEMIC
Additional Stereochemistry	No
Defined Stereocenters	0 / 1
E/Z Centers	0
Optical Activity	( + / - )

Approval Year

Substance Class	Chemical Created by `admin` on `Sat Dec 16 17:01:50 UTC 2023` Edited by `admin` on `Sat Dec 16 17:01:50 UTC 2023`
Record UNII	GR0L9S3J0F
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

RACEPINEPHRINE

Common Name

English

2-(METHYLAMINO)-1-(3,4-DIHYDROXYPHENYL)ETHANOL

Systematic Name

English

RACEPINEPHRINE [USP MONOGRAPH]

Common Name

English

DL-ADRENALINE

Common Name

English

EPINEPHRINE, DL-

Common Name

English

BENZYL ALCOHOL, 3,4-DIHYDROXY-.ALPHA.-((METHYLAMINO)METHYL)-, (±)-

Systematic Name

English

EPIRENAMINE

Common Name

English

EPINEPHRINE DL-FORM

Common Name

English

1,2-BENZENEDIOL, 4-(1-HYDROXY-2-(METHYLAMINO)ETHYL)-

Systematic Name

English

racepinefrine [INN]

Common Name

English

EPINEPHRINE DL-FORM [MI]

Common Name

English

EPINEPHRINE RACEMIC

Common Name

English

1-(3,4-DIHYDROXY)PHENYL-2-METHYLAMINOETHANOL

Common Name

English

RACEPINEFRINE

Official Name

English

Racepinefrine [WHO-DD]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C48149

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

Code System Code Type Description

RXCUI

66887

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

RxNorm

EPA CompTox

DTXSID80858965

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

INN

4553

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

CAS

8059-19-6

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

SUPERSEDED

ChEMBL

CHEMBL1740

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

SMS_ID

100000085694

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

DAILYMED

GR0L9S3J0F

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

EVMPD

SUB10238MIG

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

DRUG CENTRAL

4508

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

ECHA (EC/EINECS)

206-347-6

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

NCI_THESAURUS

C76546

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

DRUG BANK

DB11124

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

CHEBI

33568

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

CAS

329-65-7

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

MERCK INDEX

m4944

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

Merck Index

CAS

6912-68-1

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

SUPERSEDED

CAS

8060-13-7

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

SUPERSEDED

PUBCHEM

838

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

FDA UNII

GR0L9S3J0F

Created by admin on Sat Dec 16 17:01:51 UTC 2023 , Edited by admin on Sat Dec 16 17:01:51 UTC 2023

PRIMARY

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RACEPINEPHRINE HYDROCHLORIDE

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					YKH834O4BH

ENANTIOMER -> RACEMATE


					22Q832K2UN

CATECHOL O-METHYLTRANSFERASE

METABOLIC ENZYME -> SUBSTRATE


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AMINE OXIDASE (FLAVIN-CONTAINING) A

METABOLIC ENZYME -> SUBSTRATE


					NA71GR3TNV

RACEPINEFRINE, (S)-

ENANTIOMER -> RACEMATE

Related Record Type Details


					1ZE0530JEJ

METANEPHRINE, (+/-)

METABOLITE -> PARENT

Amount:

Related Record Type Details


					GR0L9S3J0F

ACTIVE MOIETY