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Hygromycin B from Streptomyces hygroscopicus - powder, BioReagent, suitable for cell culture, suitable for insect cell culture, high purity , CAS No.31282-04-9

In stock
Item Number
H432610
Grouped product items
SKU Size
Availability
Price Qty
H432610-50mg
50mg
3
$28.90
H432610-250mg
250mg
3
$99.90
H432610-1g
1g
5
$289.90
H432610-5g
5g
2
$999.90

Basic Description

Synonyms SMP1_000163 | BCBcMAP01_000235 | O-6-Amino-6-deoxy-L-glycero-D-galacto-heptopyranosylidene-(1-2-3)-O-beta-D-talopyranosyl(1-5)-2-deoxy-N3-methyl-D-streptamine | Hygromycin B, from Streptomyces hygroscopicus | GS-5543 | (2S,3R,3A'S,4S,4'S,5R,6R,6'R,7'S,7a'
Specifications & Purity BioReagent, for cell culture, for insect cell culture, powder
Biochemical and Physiological Mechanisms Mode of Action: The product acts by inhibiting protein synthesis by inducing the misreading of the m-RNA template in the prokaryote, with the potency to inhibit translation. Antimicrobial Spectrum: Hygromycin B acts against bacteria, fungi and higher euk
Storage Temp Store at 2-8°C
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade BioReagent, for cell culture, for insect cell culture
Note 注意: 潮霉素B产品应在Store at 2-8°C的温度下保存,其干燥固定形式可在Store at 2-8°C的温度下保存至少五年。其在37°C下可稳定30天。 (对于溶液)如果在Store at 2-8°C下保存,该溶液可在两年内保持稳定。
Product Description

Chemical structure: aminoglycoside Aminoglycosides are the most widely used class of antibiotics that target ribosome. Hygromycin B is an aminocyclitol antibiotic. The organism, S. hygroscopicus contains phosphotransferase (HPH) activity, which phosphorylates hygromycin B helping in autoimmunity against the toxic effects of the drug.


Application

Hygromycin B antibiotic was used for hygro resistance effect in the following cells: transfected 293T cells with mixture of plasmids at 160 μg/ml. MCF-7 ALOX12 cells at 150 μg/ml. MSCV Luciferase PGK-hygro plasmid. STAT3 Reporter HeLa Stable Cell Line (stably transfected with Luciferase gene under the control of STAT3 promoter) maintained in DMEM supplemented with 10% FBS. Hygromycin B is an aminoglycoside antibiotic isolated from Streptomyces hygroscopicus. It has been used to study protein synthesis at the level of the 70S ribosome translocation and mRNA template misreading, as an antiviral agent by selectively penetrating cells rendered permeable by virus infection and inhibiting translation, and as a selection agent for hygromycin resistance gene transformed cells. It is recommended for use as a selection agent at 100-800 μg/mL, specifically at 100 μg/mL for prokaryotes, 200 μg/mL for lower eukaryotes and 150-400 μg/mL for higher eukaryotes.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class Organooxygen compounds
Subclass Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Aminosaccharides - Aminoglycosides - Aminocyclitol glycosides
Direct Parent 2-deoxystreptamine aminoglycosides
Alternative Parents O-glycosyl compounds  Disaccharides  Dioxolopyrans  Aminocyclitols and derivatives  Ortho esters  Cyclohexylamines  Cyclohexanols  Carboxylic acid orthoesters  Oxanes  1,3-dioxolanes  1,2-aminoalcohols  Polyols  Oxacyclic compounds  Dialkylamines  Acetals  Primary alcohols  Organopnictogen compounds  Monoalkylamines  Hydrocarbon derivatives  
Molecular Framework Aliphatic heteropolycyclic compounds
Substituents 2-deoxystreptamine aminoglycoside - O-glycosyl compound - Glycosyl compound - Disaccharide - Dioxolopyran - Aminocyclitol or derivatives - Ortho ester - Cyclohexylamine - Cyclohexanol - Carboxylic acid orthoester - Oxane - Cyclitol or derivatives - Cyclic alcohol - Meta-dioxolane - Secondary alcohol - Orthocarboxylic acid derivative - 1,2-aminoalcohol - Oxacycle - Organoheterocyclic compound - Secondary amine - Polyol - Secondary aliphatic amine - Acetal - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Primary alcohol - Organonitrogen compound - Primary aliphatic amine - Amine - Alcohol - Aliphatic heteropolycyclic compound
Description This compound belongs to the class of organic compounds known as 2-deoxystreptamine aminoglycosides. These are aminoglycosides containing the 2-deoxystreptamine (1,3-diaminocyclohexane-4,5,6-triol) core.
External Descriptors Not available

Associated Targets(non-human)

Saccharomyces cerevisiae (19171 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Ustilago maydis (75 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

Pubchem Sid 504769727
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/504769727
IUPAC Name (2S,3'R,3aS,4S,4'S,5'R,6R,6'R,7S,7aS)-4-[(1R,2S,3R,5S,6R)-3-amino-2,6-dihydroxy-5-(methylamino)cyclohexyl]oxy-6'-[(1R)-1-amino-2-hydroxyethyl]-6-(hydroxymethyl)spiro[4,6,7,7a-tetrahydro-3aH-[1,3]dioxolo[4,5-c]pyran-2,2'-oxane]-3',4',5',7-tetrol
INCHI InChI=1S/C20H37N3O13/c1-23-7-2-5(21)9(26)15(10(7)27)33-19-17-16(11(28)8(4-25)32-19)35-20(36-17)18(31)13(30)12(29)14(34-20)6(22)3-24/h5-19,23-31H,2-4,21-22H2,1H3/t5-,6-,7+,8-,9+,10-,11+,12-,13+,14-,15-,16+,17+,18-,19+,20+/m1/s1
InChIKey GRRNUXAQVGOGFE-XKIAHZFYSA-N
Smiles CNC1CC(C(C(C1O)OC2C3C(C(C(O2)CO)O)OC4(O3)C(C(C(C(O4)C(CO)N)O)O)O)O)N
Isomeric SMILES CN[C@H]1C[C@H]([C@@H]([C@H]([C@@H]1O)O[C@H]2[C@@H]3[C@H]([C@H]([C@H](O2)CO)O)O[C@]4(O3)[C@@H]([C@H]([C@H]([C@H](O4)[C@@H](CO)N)O)O)O)O)N
UN Number 3462
Packing Group I
Molecular Weight 527.52
Reaxy-Rn 1335986
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1335986&ln=

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

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.

9 results found

Lot Number Certificate Type Date Item
G2315532 Certificate of Analysis May 29, 2023 H432610
G2315533 Certificate of Analysis May 29, 2023 H432610
G2315534 Certificate of Analysis May 29, 2023 H432610
G2315535 Certificate of Analysis May 29, 2023 H432610
G2315536 Certificate of Analysis May 29, 2023 H432610
G2315538 Certificate of Analysis May 29, 2023 H432610
G2315582 Certificate of Analysis May 29, 2023 H432610
G2315537 Certificate of Analysis May 29, 2023 H432610
I2410152 Certificate of Analysis May 29, 2023 H432610

Chemical and Physical Properties

Solubility H2O: 50mg/mL (As a stock solution. Stock solutions should be stored at Store at 2-8°C. Stable at 37°C for 30 days.)
Specific Rotation[α] 20° (C=1,H2O)
Melt Point(°C) 160-180°C
Molecular Weight 527.500 g/mol
XLogP3 -6.600
Hydrogen Bond Donor Count 11
Hydrogen Bond Acceptor Count 16
Rotatable Bond Count 6
Exact Mass 527.233 Da
Monoisotopic Mass 527.233 Da
Topological Polar Surface Area 272.000 Ų
Heavy Atom Count 36
Formal Charge 0
Complexity 756.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 16
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

1. Hao Zhou, Jiangbo Huang, Fang Wang.  (2023)  Increased transcription of hsa_circ_0000644 upon RUNX family transcription factor 3 downregulation participates in the malignant development of bladder cancer.  CELLULAR SIGNALLING,  104  (110590). 
2. Yong Sun, Tingting Guo, Dawei Guo, Li Guo, Li Chen, Yu Zhang, Liping Wang.  (2016)  Establishment and characterization of an MDCK cell line stably-transfected with chicken Abcb1 encoding P-glycoprotein.  RESEARCH IN VETERINARY SCIENCE,  106  (37). 

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