RACEMETYROSINE

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National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	RACEMIC
Molecular Formula	C10H13NO3
Molecular Weight	195.2151
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of RACEMETYROSINE

Structure Search

SMILES

CC(N)(CC1=CC=C(O)C=C1)C(O)=O

InChI

InChIKey=NHTGHBARYWONDQ-UHFFFAOYSA-N

InChI=1S/C10H13NO3/c1-10(11,9(13)14)6-7-2-4-8(12)5-3-7/h2-5,12H,6,11H2,1H3,(H,13,14)

HIDE SMILES / InChI

Molecular Formula	C10H13NO3
Molecular Weight	195.2151
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 `Fri Dec 15 16:19:23 UTC 2023` Edited by `admin` on `Fri Dec 15 16:19:23 UTC 2023`
Record UNII	X88TTO174Z
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

RACEMETYROSINE

Official Name

English

TYROSINE, .ALPHA.-METHYL-

Systematic Name

English

DNP-01

Code

English

RACEMETYROSINE [USAN]

Common Name

English

D,L-METYROSINE

Common Name

English

Racemetirosine [WHO-DD]

Common Name

English

RACEMETIROSINE

Official Name

English

ALPHA-METHYLTYROSINE

Systematic Name

English

DL-2-METHYL-P-TYROSINE

Common Name

English

2-(4-HYDROXYBENZYL)-2-AMINOPROPANOIC ACID

Systematic Name

English

DL-METYROSINE

Common Name

English

ALPHA-METHYL-P-TYROSINE

Common Name

English

L1-79

Code

English

.ALPHA.-METHYL-P-TYROSINE

Common Name

English

AMPT

Common Name

English

racemetirosine [INN]

Common Name

English

SM-88 COMPONENT RACEMETYROSINE

Code

English

Classification Tree Code System Code

NCI_THESAURUS

C270

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

FDA ORPHAN DRUG

677819

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

NCI_THESAURUS

C471

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

Code System Code Type Description

ECHA (EC/EINECS)

211-523-0

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

INN

4292

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

IUPHAR

6956

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

NCI_THESAURUS

C74152

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

EPA CompTox

DTXSID90859529

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

CHEBI

6912

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

WIKIPEDIA

AMPT

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

PUBCHEM

3125

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

FDA UNII

X88TTO174Z

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

EVMPD

SUB10234MIG

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

CAS

620-30-4

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

SUPERSEDED

SMS_ID

100000080287

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

ChEMBL

CHEMBL1330596

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

USAN

GH-55

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

CAS

658-48-0

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

PRIMARY

ECHA (EC/EINECS)

210-635-7

Created by admin on Fri Dec 15 16:19:23 UTC 2023 , Edited by admin on Fri Dec 15 16:19:23 UTC 2023

ALTERNATIVE

Related Record Type Details


					EPW0V0G4N1

TYROSINE 3-MONOOXYGENASE

TARGET -> INHIBITOR

Comments:

Inhibition of tyrosine hydroxylase, the rate-limiting step for catecholamine synthesis in the CNS using oral metyrosine (α-methyltyrosine or AMPT), has been reported to reduce VCFS-related psychosis.

Amount:


					DOQ0J0TPF7

ENANTIOMER -> RACEMATE

Amount:


					7510J153OT

METYROSINE, (R)-

ENANTIOMER -> RACEMATE

Amount:


					4J3KR6645M

RACEMETYROSINE HYDROCHLORIDE

SALT/SOLVATE -> PARENT

Amount:

Related Record Type Details


					X88TTO174Z

ACTIVE MOIETY

Amount: