GENTAMICIN C2

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C20H41N5O7
Molecular Weight	463.5688
Optical Activity	UNSPECIFIED
Defined Stereocenters	13 / 13
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CN[C@@H]1[C@@H](O)[C@@H](O[C@H]2[C@H](N)C[C@H](N)[C@@H](O[C@H]3O[C@@H](CC[C@H]3N)[C@@H](C)N)[C@@H]2O)OC[C@]1(C)O

InChI

InChIKey=XUFIWSHGXVLULG-IDLVJFIQSA-N

InChI=1S/C20H41N5O7/c1-8(21)12-5-4-9(22)18(30-12)31-15-10(23)6-11(24)16(13(15)26)32-19-14(27)17(25-3)20(2,28)7-29-19/h8-19,25-28H,4-7,21-24H2,1-3H3/t8-,9-,10+,11-,12+,13+,14-,15-,16+,17-,18-,19-,20+/m1/s1

HIDE SMILES / InChI

Molecular Formula	C20H41N5O7
Molecular Weight	463.5688
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	13 / 13
E/Z Centers	0
Optical Activity	UNSPECIFIED

Description
Sources: https://www.ncbi.nlm.nih.gov/pubmed/26083124 | https://www.ncbi.nlm.nih.gov/pubmed/10817690

Gentamicin C2 together with epimer C2a is a part of the antibiotic of the aminoglycoside group, gentamicin. Gentamicin C2 has a methyl group in the 6′ position. Gentamicin is a broad-spectrum antibiotic that binds to the prokaryotic ribosome, inhibiting protein synthesis in susceptible bacteria. Gentamicin is bactericidal in vitro against Gram-positive and Gram-negative bacteria.

Approval Year

PubMed

Title	Date	PubMed
Small molecules that selectively block RNA binding of HIV-1 Rev protein inhibit Rev function and viral production.	1993-09-24	8402886

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:28:28 GMT 2025` Edited by `admin` on `Mon Mar 31 18:28:28 GMT 2025`
Record UNII	3P99H114B8
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

GENTAMICIN C2

Common Name

English

GENTAMICIN C2 [MI]

Preferred Name

English

Classification Tree Code System Code

NCI_THESAURUS

C2363