HYDROXYISOLEUCINE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C6H13NO3
Molecular Weight	147.1723
Optical Activity	UNSPECIFIED
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of HYDROXYISOLEUCINE

Structure Search

SMILES

C[C@H](O)[C@H](C)[C@H](N)C(O)=O

InChI

InChIKey=OSCCDBFHNMXNME-YUPRTTJUSA-N

InChI=1S/C6H13NO3/c1-3(4(2)8)5(7)6(9)10/h3-5,8H,7H2,1-2H3,(H,9,10)/t3-,4-,5-/m0/s1

HIDE SMILES / InChI

Molecular Formula	C6H13NO3
Molecular Weight	147.1723
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	3 / 3
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

PubMed

PubMed

Title	Date	PubMed
Metabolic engineering of Escherichia coli to produce (2S, 3R, 4S)-4-hydroxyisoleucine.	2010-10	20665018
An Organocatalyzed enantioselective synthesis of (2S,3R,4S)-4-hydroxyisoleucine and its stereoisomers.	2010-04-16	20307090
A novel l-isoleucine hydroxylating enzyme, l-isoleucine dioxygenase from Bacillus thuringiensis, produces (2S,3R,4S)-4-hydroxyisoleucine.	2009-12-18	19850012
Synthesis of hydantoin analogues of (2S,3R,4S)-4-hydroxyisoleucine with insulinotropic properties.	2008-08-01	18621529

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:02:44 GMT 2025` Edited by `admin` on `Mon Mar 31 21:02:44 GMT 2025`
Record UNII	4SWT01T54O
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

4-HYDROXYISOLEUCINE (CONSTITUENT OF FENUGREEK SEED) [DSC]

Preferred Name

English

HYDROXYISOLEUCINE

Official Name

English

(4S)-4-HYDROXY-L-ISOLEUCINE

Systematic Name

English

(2S,3R,4S)-4-HYDROXYISOLEUCINE

Systematic Name

English

L-RIBONIC ACID, 2-AMINO-2,3,5-TRIDEOXY-3-METHYL-

Common Name

English

4-HYDROXYISOLEUCINE, (+)-

Systematic Name

English

4-HYDROXYISOLEUCINE [USP-RS]

Common Name

English

Classification Tree Code System Code

DSLD

3221 (Number of products:9)

Created by admin on Mon Mar 31 21:02:44 GMT 2025 , Edited by admin on Mon Mar 31 21:02:44 GMT 2025

Code System Code Type Description

MESH

C502516

Created by admin on Mon Mar 31 21:02:44 GMT 2025 , Edited by admin on Mon Mar 31 21:02:44 GMT 2025

PRIMARY

CAS

781658-23-9

Created by admin on Mon Mar 31 21:02:44 GMT 2025 , Edited by admin on Mon Mar 31 21:02:44 GMT 2025

NON-SPECIFIC STEREOCHEMISTRY

FDA UNII

4SWT01T54O

Created by admin on Mon Mar 31 21:02:44 GMT 2025 , Edited by admin on Mon Mar 31 21:02:44 GMT 2025

PRIMARY

CHEBI

78247

Created by admin on Mon Mar 31 21:02:44 GMT 2025 , Edited by admin on Mon Mar 31 21:02:44 GMT 2025

PRIMARY

RS_ITEM_NUM

1327319

Created by admin on Mon Mar 31 21:02:44 GMT 2025 , Edited by admin on Mon Mar 31 21:02:44 GMT 2025

PRIMARY

PUBCHEM

6918732

Created by admin on Mon Mar 31 21:02:44 GMT 2025 , Edited by admin on Mon Mar 31 21:02:44 GMT 2025

PRIMARY

CAS

55399-93-4

Created by admin on Mon Mar 31 21:02:44 GMT 2025 , Edited by admin on Mon Mar 31 21:02:44 GMT 2025

PRIMARY

EPA CompTox

DTXSID90203947

Created by admin on Mon Mar 31 21:02:44 GMT 2025 , Edited by admin on Mon Mar 31 21:02:44 GMT 2025

PRIMARY

CHEBI

79079

Created by admin on Mon Mar 31 21:02:44 GMT 2025 , Edited by admin on Mon Mar 31 21:02:44 GMT 2025

PRIMARY

Related Record Type Details


					654825W09Z

PARENT -> CONSTITUENT ALWAYS PRESENT

Qualification:

USP

Amount: