G 418 disulfate salt - BioReagent, for cell culture, powder , CAS No.108321-42-2

CAS: 108321-42-2 Cat. No.: G431375 Peso molecular: 692.71 Número EC: 600-864-4 PubChem CID: 16218858
Disponible para pedir
GRADE & PURITY BioReagent ? BioReagent grade — tested suitable for life-science and molecular-biology use. Use for cell culture, assays, and biochemical work needing biological compatibility. for Cell culture ? Cell-culture grade — low endotoxin and contaminants to support viable cell growth. Use in mammalian/other cell culture media and supplements. powder
Synonyms
AC-32603 | G 418 disulfate salt | (2S,3S,4S,5S)-2-[(1S,2S,3R,4S,6R)-4,6-diamino-3-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(1-hydroxyethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxy-5-methyl-4-(methylamino)oxane-3,5-diol;sulfuric acid | C20H40N4O10.2H2SO4 | G
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
G431375-1g
5
102,90US$
5g
G431375-5g
1
408,90US$
25g
G431375-25g
1
1.399,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

BioReagent, for cell culture, powder BioReagent,for Cell culture for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C,Argon charged Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 11 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Chemical structure: aminoglycoside G-418 is an aminoglycoside antibiotic, which is produced by Micromonospora rhodorangea NRRL 5326 strain. It has a broad range of antibacterial activity both in vivo and in vitro . It also shows activity against protozoa, cecal amoebiasis, and helminthes. It is commonly known as geneticin selective antibiotic.


Application

G418 disulfate is an aminoglycoside that is toxic to bacteria, yeast, protozoans and helminths. It prevents protein synthesis by blocking the elongation step in prokaryotic and eukaryotic ribosomes. It is used as a selection agent for G418 resistant bacteria or fungi after transformation.


Other Notes

Keep container tightly closed in a dry and well-ventilated place. Keep in a dry place.

Specifications

Sinónimos
AC-32603 | G 418 disulfate salt | (2S, 3S, 4S, 5S)-2-[(1S, 2S, 3R, 4S, 6R)-4, 6-diamino-3-[(2S, 3R, 4R, 5S, 6R)-3-amino-4, 5-dihydroxy-6-(1-hydroxyethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxy-5-methyl-4-(methylamino)oxane-3, 5-diol;sulfuric acid | C20H40N4O10.2H2SO4 | G
Especificaciones y pureza
BioReagent, for cell culture, powder
Mecanismos bioquímicos y fisiológicos
G-418 inhibits protein synthesis at the early stages of elongation, post-initiation, at the initiation stage of translation as well as just before the initiation stage of translation.
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Argon charged
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
BioReagent, for Cell culture
Nota
Note: This product is stable for two years when stored at 2-8°C. Stock solutions are stable for 8 days at 37°C.
Nombres e identificadores
Pubchem Sid504768374
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504768374
Sonrisas canónicasCC(C1C(C(C(C(O1)OC2C(CC(C(C2O)OC3C(C(C(CO3)(C)O)NC)O)N)N)N)O)O)O.OS(=O)(=O)O.OS(=O)(=O)O
IUPAC Name(2S,3S,4S,5S)-2-[(1S,2S,3R,4S,6R)-4,6-diamino-3-[(2S,3R,4R,5S,6R)-3-amino-4,5-dihydroxy-6-(1-hydroxyethyl)oxan-2-yl]oxy-2-hydroxycyclohexyl]oxy-5-methyl-4-(methylamino)oxane-3,5-diol;sulfuric acid
InChIKeyUHEPSJJJMTWUCP-NKCAIAFTSA-N
INCHI1S/C20H40N4O10.2H2O4S/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;2*1-5(2,3)4/h6-19,24-30H,4-5,21-23H2,1-3H3;2*(H2,1,2,3,4)/t6?,7-,8+,9+,10+,11-,12-,13-,14+,15+,16-,17-,18+,19-,20+;;/m0../s1
Isómeros SMILES CC([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O[C@@H]2[C@H](C[C@H]([C@@H]([C@H]2O)O[C@H]3[C@H]([C@@H]([C@](CO3)(C)O)NC)O)N)N)N)O)O)O.OS(=O)(=O)O.OS(=O)(=O)O
WGK Alemania 3
PubChem CID 16218858
Peso molecular 692.71

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic oxygen compounds
ClaseOrganooxygen compounds
SubclassCarbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Aminosaccharides - Aminoglycosides
Direct ParentAminocyclitol glycosides
Alternative Parents 2-deoxystreptamine aminoglycosides  O-glycosyl compounds  Aminocyclitols and derivatives  Cyclohexylamines  Cyclohexanols  Oxanes  Organic sulfuric acids  Monosaccharides  Tertiary alcohols  1,2-aminoalcohols  Oxacyclic compounds  Dialkylamines  Acetals  Organopnictogen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Amino cyclitol glycoside - 2-deoxystreptamine aminoglycoside - O-glycosyl compound - Glycosyl compound - Aminocyclitol or derivatives - Sulfuric acid - Cyclohexylamine - Cyclohexanol - Oxane - Monosaccharide - Cyclitol or derivatives - Tertiary alcohol - Organic sulfuric acid or derivatives - Cyclic alcohol - Secondary alcohol - 1,2-aminoalcohol - Oxacycle - Organoheterocyclic compound - Secondary amine - Secondary aliphatic amine - Acetal - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Primary aliphatic amine - Amine - Alcohol - Aliphatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as aminocyclitol glycosides. These are organic compounds containing an amicocyclitol moiety glycosidically linked to a carbohydrate moiety. There are two major classes of aminoglycosides containing a 2-streptamine core. They are called 4,5- and 4,6-disubstituted 2-deoxystreptamines.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

16 results found

Lot NumberCertificate TypeFechaArticulo
F2320282Certificate of AnalysisApr 02, 2026 G431375
F2320289Certificate of AnalysisApr 02, 2026 G431375
B2524392Certificate of AnalysisFeb 26, 2025 G431375
B2524393Certificate of AnalysisFeb 26, 2025 G431375
B2524394Certificate of AnalysisFeb 26, 2025 G431375
I2518073Certificate of AnalysisFeb 26, 2025 G431375
A2408502Certificate of AnalysisDec 28, 2023 G431375
A2408519Certificate of AnalysisDec 28, 2023 G431375
A2408521Certificate of AnalysisDec 28, 2023 G431375
A2408522Certificate of AnalysisDec 28, 2023 G431375
A2408524Certificate of AnalysisDec 28, 2023 G431375
K2411029Certificate of AnalysisDec 28, 2023 G431375
F2320279Certificate of AnalysisMay 30, 2023 G431375
F2320284Certificate of AnalysisMay 30, 2023 G431375
F2320286Certificate of AnalysisMay 30, 2023 G431375
L2305152Certificate of AnalysisMay 30, 2023 G431375

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Propiedades químicas y físicas
SolubilidadH2O: 100mg/mL (As a stock solution. Stock solutions should be stored at Store at 2-8°C. Stable at 37°C for 8 days.)
SensibilidadMoisture,Heat sensitive
Rotación específica [α]111 ° (C=0.3, H2O)
Punto de fusión (°C)138-144°C
Peso molecular692.700 g/mol
XLogP3
Hydrogen Bond Donor Count14
Hydrogen Bond Acceptor Count22
Rotatable Bond Count6
Exact Mass692.209 Da
Monoisotopic Mass692.209 Da
Topological Polar Surface Area414.000 Ų
Heavy Atom Count44
Formal Charge0
Complexity763.000
Isotope Atom Count0
Defined Atom Stereocenter Count14
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count3
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Han Sijia, Jin Xueying, Hu Tianyu, Chi Feng.  (2023)  ARHGAP25 suppresses the development of breast cancer by an ARHGAP25/Wnt/ASCL2 feedback loop.  CARCINOGENESIS,      [PMID:37326327] [10.1093/carcin/bgad042]
2. Sijia Han, Xueying Jin, Tianyu Hu, Feng Chi.  (2023)  LAPTM5 regulated by FOXP3 promotes the malignant phenotypes of breast cancer through activating the Wnt/β‑catenin pathway.  ONCOLOGY REPORTS,  49  (3): (1-14).  [PMID:36799186] [10.3892/or.2023.8497]
3. Jing Zhou, Tongyu Wu, Chun Li, Zhuozhou Hu, Liang Han, Xiangxiang Li, Jingjing Liu, Wenyang Zhao, Jia Kang, Xinping Chen.  (2023)  Alfuzosin ameliorates diabetes by boosting PGK1 activity in diabetic mice.  LIFE SCIENCES,      [PMID:36758669] [10.1016/j.lfs.2023.121491]
4. Zhuozhou Hu, Jing Zhou, Liang Han, Xiangxiang Li, Chun Li, Tongyu Wu, Jingjing Liu, Wenyang Zhao, Jia Kang, Xinping Chen.  (2022)  Acyclovir alleviates insulin resistance via activating PKM1 in diabetic mice.  LIFE SCIENCES,      [PMID:35751919] [10.1016/j.lfs.2022.120725]
5. Jie Zhu, Kun Yang, Aijie Liu, Xiaoxue Lu, Linsong Yang, Qinghuan Zhao.  (2020)  Highly secretory expression of recombinant cowpea chlorotic mottle virus capsid proteins in Pichia pastoris and in-vitro encapsulation of ruthenium nanoparticles for catalysis.  PROTEIN EXPRESSION AND PURIFICATION,      [PMID:32534017] [10.1016/j.pep.2020.105679]
6. Wang Shuai, He Ting, Luo Ya, Ren Kexin, Shen Huanming, Hou Lingfeng, Wei Yixin, Fu Tong, Xie Wenlong, Wang Peng, Hu Jie, Zhu Yu, Huang Zhengrong, Li Qiyuan, Li Weihua, Guo Huiling, Li Boan.  (2024)  SOX4 facilitates brown fat development and maintenance through EBF2-mediated thermogenic gene program in mice.  CELL DEATH AND DIFFERENTIATION,      [PMID:39402212] [10.1038/s41418-024-01397-0]
7. Jiankun Zang, Yousheng Wu, Xuanlin Su, Kaiwei Cai, Man Ke, Niu He, Huili Zhu, Zefeng Tan, Jielin Zhu, Wensheng He, Min Peng, Shiqing Zhang, Hongcheng Mai, Anding Xu, Dan Lu.  (2024)  FUS Selectively Facilitates circRNAs Packing into Small Extracellular Vesicles within Hypoxia Neuron.  Advanced Science,      [PMID:38924471] [10.1002/advs.202404822]
8. Jiaojiao He, Haoyang Zhou, Jine Liang, Kadireya Tuerxun, Zhuoling Ding, Shishui Zhou.  (2024)  HOM2 Deletion by CRISPR-Cas9 in Saccharomyces cerevisiae for Decreasing Higher Alcohols in Whiskey.  Fermentation-Basel,  10  (11): (589).  [PMID:] [10.3390/fermentation10110589]
9. Xinrui Meng, Jingjing Liu, Jia Kang, Menghan Wang, Zhanghui Guan, Dong Tian, Xinping Chen.  (2024)  Lamivudine protects mice from gastric ulcer by activating PGK1 to suppress ferroptosis.  BIOCHEMICAL PHARMACOLOGY,      [PMID:39029631] [10.1016/j.bcp.2024.116440]
10. Wu Liang, Wen Yongdi, Chen Wenying, Yan Tongshuai, Tian Xiaofei, Zhou Shishui.  (2021)  Simultaneously deleting ADH2 and THI3 genes of Saccharomyces cerevisiae for reducing the yield of acetaldehyde and fusel alcohols.  FEMS MICROBIOLOGY LETTERS,  368  (15):   [PMID:34410369] [10.1093/femsle/fnab094]
11. Jiejing Tang, Hang Zhou, Chen Jiao, Hongye Li.  (2025)  Functional Characterization of Deubiquitinase UBP Family and Proteomic Analysis of Aaubp14-Mediated Pathogenicity Mechanism in Alternaria alternata.  Journal of Fungi,  11  (7): (495).  [PMID:40985402] [10.3390/jof11070495]
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