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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

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

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
ATP-binding cassette transporters as pitfalls in selection of transgenic cells.
2010-04-15
Stop codon read-through of a methylmalonic aciduria mutation.
2009-08
Translational readthrough by the aminoglycoside geneticin (G418) modulates SMN stability in vitro and improves motor function in SMA mice in vivo.
2009-04-01
G418-mediated ribosomal read-through of a nonsense mutation causing autosomal recessive proximal renal tubular acidosis.
2008-09
Restoration of W1282X CFTR activity by enhanced expression.
2007-09
Intracellular readthrough of nonsense mutations by aminoglycosides in coagulation factor VII.
2006-06
Aminoglycosides decrease glutathione peroxidase-1 activity by interfering with selenocysteine incorporation.
2006-02-10
Correction of ATM gene function by aminoglycoside-induced read-through of premature termination codons.
2004-11-02
Cytochrome c release and endoplasmic reticulum stress are involved in caspase-dependent apoptosis induced by G418.
2004-07
Aminoglycoside-mediated rescue of a disease-causing nonsense mutation in the V2 vasopressin receptor gene in vitro and in vivo.
2004-05-01
Classification and rescue of ROMK mutations underlying hyperprostaglandin E syndrome/antenatal Bartter syndrome.
2003-09
Aminoglycoside pretreatment partially restores the function of truncated V(2) vasopressin receptors found in patients with nephrogenic diabetes insipidus.
2002-11
Paromomycin and geneticin inhibit intracellular Cryptosporidium parvum without trafficking through the host cell cytoplasm: implications for drug delivery.
1998-08
Inhibition of HIV type 1 production by hygromycin B.
1998-07-01
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
ANTIBIOTIC G 418
Preferred 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
G-418
Common Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 204605
Created by admin on Mon Mar 31 17:47:15 GMT 2025 , Edited by admin on Mon Mar 31 17:47:15 GMT 2025
Code System Code Type Description
PUBCHEM
123865
Created by admin on Mon Mar 31 17:47:15 GMT 2025 , Edited by admin on Mon Mar 31 17:47:15 GMT 2025
PRIMARY
EPA CompTox
DTXSID10198129
Created by admin on Mon Mar 31 17:47:15 GMT 2025 , Edited by admin on Mon Mar 31 17:47:15 GMT 2025
PRIMARY
FDA UNII
A08F5XTI6G
Created by admin on Mon Mar 31 17:47:15 GMT 2025 , Edited by admin on Mon Mar 31 17:47:15 GMT 2025
PRIMARY
CHEBI
42768
Created by admin on Mon Mar 31 17:47:15 GMT 2025 , Edited by admin on Mon Mar 31 17:47:15 GMT 2025
PRIMARY
WIKIPEDIA
G418
Created by admin on Mon Mar 31 17:47:15 GMT 2025 , Edited by admin on Mon Mar 31 17:47:15 GMT 2025
PRIMARY
CAS
49863-47-0
Created by admin on Mon Mar 31 17:47:15 GMT 2025 , Edited by admin on Mon Mar 31 17:47:15 GMT 2025
PRIMARY
DRUG BANK
DB04263
Created by admin on Mon Mar 31 17:47:15 GMT 2025 , Edited by admin on Mon Mar 31 17:47:15 GMT 2025
PRIMARY