Compound

3-chloro-L-tyrosine

An L-α-amino acid zwitterion obtained by transfer of a proton from the carboxy to the amino group of 3-chloro-L-tyrosine; major species at pH 7.3.

Definition from ChEBI (CHEBI:189422), read 2026-09-23. CC BY 4.0.

CHEBI:189422ChEBI

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Structure

2D depiction · 3D model shown

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A generated conformer of 3-chloro-L-tyrosine — one low-energy arrangement PubChem computed, not a measured structure. Hydrogens are not drawn; the formula counts them.

Class: Organic compound
Formula: C9H10ClNO3
Mass: 215.636 g/mol
Charge: 0
InChIKey: ACWBBAGYTKWBCD-ZETCQYMHSA-N
SMILES: [NH3+][C@@H](Cc1ccc(O)c(Cl)c1)C(=O)[O-]
Look it up: ChEBI PubChem By InChIKey

Identity from ChEBI, geometry from PubChem. Not evidence.

What it touches on the way

Mechanistic reach

1 entity

1 entities reached.

0 reported hops1 assembled from the scaffold

IYDProteinUNIPROT:Q6PHW0substrate ofInferred only5 paths5 endpoints

What the reference databases state

Statements

1 statement

1 statement · 1 reference database · Subject: 3-chloro-L-tyrosine · Sources: Rhea

Order

3-chloro-L-tyrosine is a substrate of IYDProteinRhea RHEA:70343Inferred only

Reactions

1 reaction

L-tyrosine+chloride+NADP(3-)3-chloro-L-tyrosine+NADPH(4-)
Catalysed by IYD
Reaction pageRight to leftBalance undeterminable
Rhea RHEA:70343CC BY 4.0Reference data

Other names

3 names

Resolves to: 3-chloro-L-tyrosine

Also called: (2S)-2-ammonio-3-(3-chloro-4-hydroxyphenyl)propanoate3-chloro-L-Tyr zwitterion
Systematic name: (2S)-2-azaniumyl-3-(3-chloro-4-hydroxyphenyl)propanoate