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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H40N4O10
Molecular Weight 496.5524
Optical Activity UNSPECIFIED
Defined Stereocenters 15 / 15
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of GENETICIN

SMILES

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

InChI

InChIKey=BRZYSWJRSDMWLG-DJWUNRQOSA-N
InChI=1S/C20H40N4O10/c1-6(25)14-11(27)10(26)9(23)18(32-14)33-15-7(21)4-8(22)16(12(15)28)34-19-13(29)17(24-3)20(2,30)5-31-19/h6-19,24-30H,4-5,21-23H2,1-3H3/t6-,7+,8-,9-,10-,11+,12+,13-,14-,15-,16+,17-,18-,19-,20+/m1/s1

HIDE SMILES / InChI

Description
Curator's Comment: description was created based on several sources, including: http://www.invivogen.com/g418 | http://www.g418-evopure.com/Technical.html

Geneticin (G-418) is produced by Micromonospora phodorangea. The antibiotic has brad spectrum antibacterial activity similar to gentamicins and other previously described aminoglycosides but of particular interest because of its high activity against protozoa, amoebae, tapeworm and pinworm infections in mice. G418 blocks polypeptide synthesis by inhibiting the elongation step in both prokaryotic and eukaryotic cells. G418 is commonly used in laboratory research to select genetically engineered cells.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Paromomycin and geneticin inhibit intracellular Cryptosporidium parvum without trafficking through the host cell cytoplasm: implications for drug delivery.
1998 Aug
Inhibition of HIV type 1 production by hygromycin B.
1998 Jul 1
Aminoglycoside pretreatment partially restores the function of truncated V(2) vasopressin receptors found in patients with nephrogenic diabetes insipidus.
2002 Nov
Classification and rescue of ROMK mutations underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome.
2003 Sep
Cytochrome c release and endoplasmic reticulum stress are involved in caspase-dependent apoptosis induced by G418.
2004 Jul
Aminoglycoside-mediated rescue of a disease-causing nonsense mutation in the V2 vasopressin receptor gene in vitro and in vivo.
2004 May 1
Correction of ATM gene function by aminoglycoside-induced read-through of premature termination codons.
2004 Nov 2
Aminoglycosides decrease glutathione peroxidase-1 activity by interfering with selenocysteine incorporation.
2006 Feb 10
Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII.
2006 Jun
Restoration of W1282X CFTR activity by enhanced expression.
2007 Sep
G418-mediated ribosomal read-through of a nonsense mutation causing autosomal recessive proximal renal tubular acidosis.
2008 Sep
Translational readthrough by the aminoglycoside geneticin (G418) modulates SMN stability in vitro and improves motor function in SMA mice in vivo.
2009 Apr 1
Stop codon read-through of a methylmalonic aciduria mutation.
2009 Aug
ATP-binding cassette transporters as pitfalls in selection of transgenic cells.
2010 Apr 15
Patents

Patents

Sample Use Guides

4 mg/kg to neonatal mice from postnatal day (PND) 5–13.
Route of Administration: Intraperitoneal
In Vitro Use Guide
All of the Saccharomyces sp. strains, including the brewing strains, were found to be susceptible to G418 in the concentration range of 150 to 500 ug/ml. Of the three Schwanniomyces species investigated, only Schwanniomyces castellii (strain 1402) was found to be resistant to G418 at concentrations up to 1 mg/ml.
Name Type Language
GENETICIN
Common Name English
G418
Common Name English
ANTIBIOTIC G-418
Common Name English
D-STREPTAMINE, O-2-AMINO-2,7-DIDEOXY-D-GLYCERO-.ALPHA.-D-GLUCO-HEPTOPYRANOSYL-(1->4)-O-(3-DEOXY-4-C-METHYL-3-(METHYLAMINO)-.BETA.-L-ARABINOPYRANOSYL-(1->6))-2-DEOXY-
Common Name English
ANTIBIOTIC G 418
Common Name English
G-418
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 204605
Created by admin on Fri Dec 15 15:07:23 GMT 2023 , Edited by admin on Fri Dec 15 15:07:23 GMT 2023
Code System Code Type Description
PUBCHEM
123865
Created by admin on Fri Dec 15 15:07:23 GMT 2023 , Edited by admin on Fri Dec 15 15:07:23 GMT 2023
PRIMARY
EPA CompTox
DTXSID10198129
Created by admin on Fri Dec 15 15:07:23 GMT 2023 , Edited by admin on Fri Dec 15 15:07:23 GMT 2023
PRIMARY
FDA UNII
A08F5XTI6G
Created by admin on Fri Dec 15 15:07:23 GMT 2023 , Edited by admin on Fri Dec 15 15:07:23 GMT 2023
PRIMARY
CHEBI
42768
Created by admin on Fri Dec 15 15:07:23 GMT 2023 , Edited by admin on Fri Dec 15 15:07:23 GMT 2023
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WIKIPEDIA
G418
Created by admin on Fri Dec 15 15:07:23 GMT 2023 , Edited by admin on Fri Dec 15 15:07:23 GMT 2023
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CAS
49863-47-0
Created by admin on Fri Dec 15 15:07:23 GMT 2023 , Edited by admin on Fri Dec 15 15:07:23 GMT 2023
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DRUG BANK
DB04263
Created by admin on Fri Dec 15 15:07:23 GMT 2023 , Edited by admin on Fri Dec 15 15:07:23 GMT 2023
PRIMARY