MYCAROSE, DL-

Details

Stereochemistry	RACEMIC
Molecular Formula	C7H14O4
Molecular Weight	162.1837
Optical Activity	( + / - )
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

SMILES

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

InChI

InChIKey=JYAQWANEOPJVEY-LYFYHCNISA-N

InChI=1S/C7H14O4/c1-5(9)6(10)7(2,11)3-4-8/h4-6,9-11H,3H2,1-2H3/t5-,6-,7+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C7H14O4
Molecular Weight	162.1837
Charge	0
Count	MOL RATIO 1 MOL RATIO (average)

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

Approval Year

PubMed

Show entries

Title	Date	PubMed
Isolation and structure elucidation of vicenistatin M, and importance of the vicenisamine aminosugar for exerting cytotoxicity of vicenistatin.	2001 Mar	11372778
Ketopremithramycins and ketomithramycins, four new aureolic acid-type compounds obtained upon inactivation of two genes involved in the biosynthesis of the deoxysugar moieties of the antitumor drug mithramycin by Streptomyces argillaceus, reveal novel insights into post-PKS tailoring steps of the mithramycin biosynthetic pathway.	2002 Feb 27	11853433
Biosynthesis of TDP-l-mycarose: the specificity of a single enzyme governs the outcome of the pathway.	2005 Jul 6	15984840
A two-stage one-pot enzymatic synthesis of TDP-L-mycarose from thymidine and glucose-1-phosphate.	2006 Feb 8	16448097
Bioassay-guided evolution of glycosylated macrolide antibiotics in Escherichia coli.	2007 Feb	17298179

Showing 1 to 5 of 7 entries

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Patents

Substance Class	Chemical
Record UNII	I71I3DG1W1
Record Status	`Validated (UNII)`
Record Version

Show entries

Name

Type

Language

MYCAROSE, DL-

Common Name

English

MYCAROSE DL- FORM [MI]

Preferred Name

English

MYCAROSE, (±)-

Common Name

English

RIBO-HEXOSE, 2,6-DIDEOXY-3-C-METHYL-

Systematic Name

English

Showing 1 to 4 of 4 entries

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Code System

Code

Type

Description

FDA UNII

I71I3DG1W1

PRIMARY

CAS

92345-04-5

PRIMARY

Showing 1 to 2 of 2 entries

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