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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H26N4O6.4ClH
Molecular Weight 468.202
Optical Activity UNSPECIFIED
Defined Stereocenters 10 / 10
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NEAMINE HYDROCHLORIDE

SMILES

Cl.Cl.Cl.Cl.[H][C@]2(O[C@@H]1[C@@H](N)C[C@@H](N)[C@H](O)[C@H]1O)O[C@H](CN)[C@@H](O)[C@H](O)[C@H]2N

InChI

InChIKey=YHGAXELMYJIVJN-OXGCEHIISA-N
InChI=1S/C12H26N4O6.4ClH/c13-2-5-8(18)9(19)6(16)12(21-5)22-11-4(15)1-3(14)7(17)10(11)20;;;;/h3-12,17-20H,1-2,13-16H2;4*1H/t3-,4+,5-,6-,7+,8-,9-,10-,11-,12-;;;;/m1..../s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C12H26N4O6
Molecular Weight 322.358
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 10 / 10
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Screening for new compounds with antiherpes activity.
1984 Oct
Small molecules that selectively block RNA binding of HIV-1 Rev protein inhibit Rev function and viral production.
1993 Sep 24
Synthesis of biomimetic analogs of neomycin B: potential inhibitors of the HIV RNA Rev response element.
2000 Jan-Feb
Study of aminoglycoside-nucleic acid interactions by an HPLC method.
2001 Apr 23
Aminoglycoside antibiotics, neamine and its derivatives as potent inhibitors for the RNA-protein interactions derived from HIV-1 activators.
2001 Feb 26
An efficient synthesis of mimetics of neamine for RNA recognition.
2001 May 31
Design of novel antibiotics that bind to the ribosomal acyltransfer site.
2002 Apr 3
Crystal structure of geneticin bound to a bacterial 16S ribosomal RNA A site oligonucleotide.
2003 Feb 28
Regioselective glycosylation of neamine core: a facile entry to kanamycin B related analogues.
2004 Feb 19
Neamine inhibits xenografic human tumor growth and angiogenesis in athymic mice.
2005 Dec 15
Neamine derivatives having a nucleobase with a lysine or an arginine as a linker, their synthesis and evaluation as potential inhibitors for HIV TAR-Tat.
2006 Apr 15
A molecular dynamics simulation study of an aminoglycoside/A-site RNA complex: conformational and hydration patterns.
2006 Aug
Cationic polyamines inhibit anthrax lethal factor protease.
2006 Jun 8
Selectively guanidinylated derivatives of neamine. Syntheses and inhibition of anthrax lethal factor protease.
2006 Oct 1
Mechanism of RNA cleavage catalyzed by sequence specific polyamide nucleic acid-neamine conjugate.
2007 Fall
Synthesis of a neamine dimer targeting the dimerization initiation site of HIV-1 RNA.
2007 Oct 25
Fluorescence correlation spectroscopy at single molecule level on the Tat-TAR complex and its inhibitors.
2008 Jan
Studies on the synthesis of neamine-dinucleosides and neamine-PNA conjugates and their interaction with RNA.
2008 Oct 15
Chiral ligand-exchange chromatography of amino acids using porous graphitic carbon coated with a dinaphthyl derivative of neamine.
2009 Jan
Neamine inhibits cell proliferation, migration, and invasion in H7402 human hepatoma cells.
2010 Dec
Aminoglycoside binding to Oxytricha nova telomeric DNA.
2010 Nov 16
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:03:17 GMT 2023
Edited
by admin
on Fri Dec 15 15:03:17 GMT 2023
Record UNII
EIU453IDVS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NEAMINE HYDROCHLORIDE
Common Name English
D-STREPTAMINE, 2-DEOXY-4-O-(2,6-DIAMINO-2,6-DIDEOXY-.ALPHA.-D-GLUCOPYRANOSYL)-, HYDROCHLORIDE (1:4)
Common Name English
NEOMYCIN A, TETRAHYDROCHLORIDE
Common Name English
NEOMYCIN A TETRAHYDROCHLORIDE
Common Name English
D-STREPTAMINE, 2-DEOXY-4-O-(2,6-DIAMINO-2,6-DIDEOXY-.ALPHA.-D-GLUCOPYRANOSYL)-, TETRAHYDROCHLORIDE
Common Name English
Code System Code Type Description
FDA UNII
EIU453IDVS
Created by admin on Fri Dec 15 15:03:17 GMT 2023 , Edited by admin on Fri Dec 15 15:03:17 GMT 2023
PRIMARY
PUBCHEM
11784617
Created by admin on Fri Dec 15 15:03:17 GMT 2023 , Edited by admin on Fri Dec 15 15:03:17 GMT 2023
PRIMARY
CAS
15446-43-2
Created by admin on Fri Dec 15 15:03:17 GMT 2023 , Edited by admin on Fri Dec 15 15:03:17 GMT 2023
PRIMARY
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ACTIVE MOIETY