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Streptomycin sulfate - 720 I.U./mg, high purity , CAS No.3810-74-0

    Grade & Purity:
  • 720 I.U./mg
In stock
Item Number
S105491
Grouped product items
SKU Size
Availability
Price Qty
S105491-25g
25g
≥10
$22.90
S105491-100g
100g
4
$82.90
S105491-500g
500g
3
$198.90

Basic Description

Synonyms STREP SOL | STREPTOMYCIN SULFATE [GREEN BOOK] | D-STREPTAMINE, O-2-DEOXY-2-(METHYLAMINO)-alpha-L-GLUCOPYRANOSYL-(1->2)-O-5-DEOXY-3-C-FORMYL-alpha-L-LYXOFURANOSYL-(1->4)-N,N'-BIS(AMINOIMINOMETHYL)-, SULPHATE (2:3) (SALT) | Streptomycin A sulfate | CCRIS 5
Specifications & Purity 720 I.U./mg
Biochemical and Physiological Mechanisms Mode of Action: Inhibits prokaryote protein synthesis. Binds to S12 protein of 30S ribosomal subunit, preventing the transition from initiation complex to chain-elongating ribosome, causing miscoding or inhibiting initiation. Mode of Resistance: Mutation
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.
Product Description

Streptomycin sulfate is an aminocyclitol glycoside antibiotic which interferes with protein synthesis in prokaryotes. This antibiotic is effective against both gram-positive and gram-negative bacteria and is frequently used in cell culture media. Streptomycin inhibits protein synthesis by binding to the 30S ribosomal subunit at the S12 protein thereby inducing a misreading of the genetic code, inhibiting the initiation of translation of DNA which then results in death for a susceptible bacterium.
An antibiotic for cell culture.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organic oxygen compounds
Class Organooxygen compounds
Subclass Carbohydrates and carbohydrate conjugates
Intermediate Tree Nodes Aminosaccharides - Aminoglycosides
Direct Parent Aminocyclitol glycosides
Alternative Parents O-glycosyl compounds  Cyclohexanols  Cyclitols and derivatives  Monosaccharides  Organic sulfuric acids  Oxanes  Tetrahydrofurans  Tertiary alcohols  Guanidines  1,2-aminoalcohols  Oxacyclic compounds  Acetals  Dialkylamines  Carboximidamides  Polyols  Propargyl-type 1,3-dipolar organic compounds  Organopnictogen compounds  Aldehydes  Organic oxides  Hydrocarbon derivatives  Primary alcohols  
Molecular Framework Not available
Substituents Amino cyclitol glycoside - Glycosyl compound - O-glycosyl compound - Cyclohexanol - Sulfuric acid - Cyclitol or derivatives - Monosaccharide - Oxane - Cyclic alcohol - Organic sulfuric acid or derivatives - Tertiary alcohol - Tetrahydrofuran - Secondary alcohol - 1,2-aminoalcohol - Guanidine - Carboximidamide - Secondary amine - Secondary aliphatic amine - Polyol - Oxacycle - Organoheterocyclic compound - Organic 1,3-dipolar compound - Acetal - Propargyl-type 1,3-dipolar organic compound - Organic oxide - Primary alcohol - Alcohol - Hydrocarbon derivative - Aldehyde - Amine - Organic nitrogen compound - Organopnictogen compound - Organonitrogen compound - Carbonyl group - Aliphatic heteromonocyclic compound
Description This 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

Associated Targets(non-human)

Salmonella paratyphi (588 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Agrobacterium tumefaciens (620 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Micrococcus luteus (7463 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Staphylococcus haemolyticus (1695 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Salmonella typhi (4293 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Streptococcus mutans (2687 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Bacillus subtilis (32866 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mycobacterium tuberculosis (203094 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mycolicibacterium smegmatis (8003 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Xanthomonas euvesicatoria (74 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 488182553
Pubchem Sid Url https://pubchem.ncbi.nlm.nih.gov/substance/488182553
IUPAC Name 2-[(1R,2R,3S,4R,5R,6S)-3-(diaminomethylideneamino)-4-[(2R,3R,4R,5S)-3-[(2S,3S,4S,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-(methylamino)oxan-2-yl]oxy-4-formyl-4-hydroxy-5-methyloxolan-2-yl]oxy-2,5,6-trihydroxycyclohexyl]guanidine;sulfuric acid
INCHI InChI=1S/2C21H39N7O12.3H2O4S/c2*1-5-21(36,4-30)16(40-17-9(26-2)13(34)10(31)6(3-29)38-17)18(37-5)39-15-8(28-20(24)25)11(32)7(27-19(22)23)12(33)14(15)35;3*1-5(2,3)4/h2*4-18,26,29,31-36H,3H2,1-2H3,(H4,22,23,27)(H4,24,25,28);3*(H2,1,2,3,4)/t2*5-,6-,7+,8-,9-,10-,11+,12-,13-,14+,15+,16-,17-,18-,21+;;;/m00.../s1
InChIKey QTENRWWVYAAPBI-YCRXJPFRSA-N
Smiles CC1C(C(C(O1)OC2C(C(C(C(C2O)O)N=C(N)N)O)N=C(N)N)OC3C(C(C(C(O3)CO)O)O)NC)(C=O)O.CC1C(C(C(O1)OC2C(C(C(C(C2O)O)N=C(N)N)O)N=C(N)N)OC3C(C(C(C(O3)CO)O)O)NC)(C=O)O.OS(=O)(=O)O.OS(=O)(=O)O.OS(=O)(=O)O
Isomeric SMILES C[C@H]1[C@@]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H]([C@@H]([C@H]2O)O)N=C(N)N)O)N=C(N)N)O[C@H]3[C@H]([C@@H]([C@H]([C@@H](O3)CO)O)O)NC)(C=O)O.C[C@H]1[C@@]([C@H]([C@@H](O1)O[C@@H]2[C@H]([C@@H]([C@H]([C@@H]([C@H]2O)O)N=C(N)N)O)N=C(N)N)O[C@H]3[C@H]([C@@H]([C@H]([C@@H](O3)CO)O)O)NC)(C=O)O.OS(=O)(=O)O.OS(=O)(=O)O.OS(=O)(=O)O
WGK Germany 3
RTECS WK4990000
Alternate CAS 57-92-1
PubChem CID 19648
Molecular Weight 1457.38
Beilstein 3894995

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.

28 results found

Lot Number Certificate Type Date Item
A2508344 Certificate of Analysis Dec 20, 2024 S105491
A2508334 Certificate of Analysis Dec 20, 2024 S105491
A2508345 Certificate of Analysis Dec 20, 2024 S105491
H2423129 Certificate of Analysis Aug 12, 2024 S105491
H2423130 Certificate of Analysis Aug 12, 2024 S105491
F2418058 Certificate of Analysis Jun 11, 2024 S105491
F2418059 Certificate of Analysis Jun 11, 2024 S105491
C2419516 Certificate of Analysis Mar 01, 2024 S105491
C2419376 Certificate of Analysis Mar 01, 2024 S105491
J2309607 Certificate of Analysis Sep 18, 2023 S105491
J2309623 Certificate of Analysis Sep 18, 2023 S105491
G23131273 Certificate of Analysis Jul 08, 2023 S105491
G23131232 Certificate of Analysis Jul 08, 2023 S105491
G23131235 Certificate of Analysis Jul 08, 2023 S105491
G23131236 Certificate of Analysis Jul 08, 2023 S105491
C23031285 Certificate of Analysis Feb 13, 2023 S105491
C23031284 Certificate of Analysis Feb 13, 2023 S105491
C23031267 Certificate of Analysis Feb 13, 2023 S105491
A2303543 Certificate of Analysis Nov 23, 2022 S105491
A2303545 Certificate of Analysis Nov 23, 2022 S105491
A2303229 Certificate of Analysis Nov 23, 2022 S105491
A2303238 Certificate of Analysis Nov 23, 2022 S105491
H2209633 Certificate of Analysis Jul 22, 2022 S105491
H2209631 Certificate of Analysis Jul 22, 2022 S105491
H2209632 Certificate of Analysis Jul 22, 2022 S105491
F2116369 Certificate of Analysis Jun 21, 2021 S105491
F2116368 Certificate of Analysis Jun 21, 2021 S105491
F2118118 Certificate of Analysis Jun 21, 2021 S105491

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Chemical and Physical Properties

Solubility Soluble in water (50 mg/ml).
Specific Rotation[α] -85° (C=1,H2O)
Melt Point(°C) 250 °C
Molecular Weight 1457.400 g/mol
XLogP3
Hydrogen Bond Donor Count 30
Hydrogen Bond Acceptor Count 42
Rotatable Bond Count 18
Exact Mass 1456.43 Da
Monoisotopic Mass 1456.43 Da
Topological Polar Surface Area 922.000 Ų
Heavy Atom Count 95
Formal Charge 0
Complexity 1020.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 30
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 5

Citations of This Product

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4. Li Daoyuan, Wang Run, You Meng, Chen Naidong, Sun Li, Chen Naifu.  (2023)  The antimicrobial effect and mechanism of the Artemisia argyi essential oil against bacteria and fungus.  BRAZILIAN JOURNAL OF MICROBIOLOGY,    (1-9). 
5. Dongxu Yuan, Bingbing Liu, Xinsong Yuan, Leilei Feng, Xudong Xu, Jialin Zhu, Zhengjie Chen, Renhao Xu, Jiao Chen, Gang Xu, Jianping Lin, Lirong Yang, Mian Li, Jiazhang Lian, Mianbin Wu.  (2023)  Multisite Mutation of the Escherichia coli cAMP Receptor Protein: Enhancing Xylitol Biosynthesis by Activating Xylose Catabolism and Improving Strain Tolerance.  JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY,  71  (45): (17226–17234). 
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28. Yunyan Ren, Zhefeng Fan.  (2023)  Synthesis of fluorescent probe based on molecularly imprinted polymers on nitrogen-doped carbon dots for determination of tobramycin in milk.  FOOD CHEMISTRY,  416  (135792). 
29. Chuanyu Zhu, Zhongmin Feng, Yupu Meng, Min Wang, Zhuqing Wang.  (2023)  Effective removal of lead and copper ions from water using a novel sodium alginate–streptomycin sulfate composite aerogel.  NEW JOURNAL OF CHEMISTRY,  47  (14): (6739-6748). 
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