Viomycin sulfate , 70S ribosome inhibitor, CAS No.24356-69-2, 70S ribosome inhibitor

CAS: 24356-69-2 Cat. No.: V671345 Molecular Weight: 783.8 PubChem CID: 135524783
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Synonyms
VIOMYCIN SULFATE | DSSTox_CID_26290 | Viomycin-sulfat | VIOMYCIN SULFATE [ORANGE BOOK] | NSC-760360 | DTXSID8046290 | UNII-LKO141R05V | (3S)-3,6-diamino-N-[(3S,6Z,9S,12S,15S)-3-[(4R,6S)-2-amino-6-hydroxy-1,4,5,6-tetrahydropyrimidin-4-yl]-6-[(carbamoylamin
Storage
Room temperature
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Size
Status
Price
Qty
1mg
V671345-1mg
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
$999.90
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Why this grade

for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
VIOMYCIN SULFATE | DSSTox_CID_26290 | Viomycin-sulfat | VIOMYCIN SULFATE [ORANGE BOOK] | NSC-760360 | DTXSID8046290 | UNII-LKO141R05V | (3S)-3, 6-diamino-N-[(3S, 6Z, 9S, 12S, 15S)-3-[(4R, 6S)-2-amino-6-hydroxy-1, 4, 5, 6-tetrahydropyrimidin-4-yl]-6-[(carbamoylamin
Storage
Room temperature
Action Type
INHIBITOR
Mechanism of action
70S ribosome inhibitor
Names and Identifiers
Canonical SmilesC1C(N=C(NC1O)N)C2C(=O)NCC(C(=O)NC(C(=O)NC(C(=O)NC(=CNC(=O)N)C(=O)N2)CO)CO)NC(=O)CC(CCCN)N.OS(=O)(=O)O
IUPAC Name(3S)-3,6-diamino-N-[(3S,6Z,9S,12S,15S)-3-[(4R,6S)-2-amino-6-hydroxy-1,4,5,6-tetrahydropyrimidin-4-yl]-6-[(carbamoylamino)methylidene]-9,12-bis(hydroxymethyl)-2,5,8,11,14-pentaoxo-1,4,7,10,13-pentazacyclohexadec-15-yl]hexanamide;sulfuric acid
InChIKeyAQONYROJHRNYQQ-QMAPKBLTSA-N
INCHI1S/C25H43N13O10.H2O4S/c26-3-1-2-10(27)4-16(41)32-12-6-30-23(47)18(11-5-17(42)37-24(28)36-11)38-20(44)13(7-31-25(29)48)33-21(45)14(8-39)35-22(46)15(9-40)34-19(12)43;1-5(2,3)4/h7,10-12,14-15,17-18,39-40,42H,1-6,8-9,26-27H2,(H,30,47)(H,32,41)(H,33,45)(
Isomeric SMILES C1[C@@H](N=C(N[C@H]1O)N)[C@H]2C(=O)NC[C@@H](C(=O)N[C@H](C(=O)N[C@H](C(=O)N/C(=C\NC(=O)N)/C(=O)N2)CO)CO)NC(=O)C[C@H](CCCN)N.OS(=O)(=O)O
PubChem CID 135524783
Molecular Weight 783.8

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.

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🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

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Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganic acids and derivatives
ClassPeptidomimetics
SubclassHybrid peptides
Intermediate Tree Nodes Not available
Direct ParentHybrid peptides
Alternative Parents N-acyl-alpha amino acids and derivatives  Macrolactams  Beta amino acids and derivatives  Organic sulfuric acids  N-acyl amines  Hydropyrimidines  Vinylogous amides  Ureas  Secondary carboxylic acid amides  Lactams  Guanidines  Propargyl-type 1,3-dipolar organic compounds  Alkanolamines  Azacyclic compounds  Carboximidamides  Hydrocarbon derivatives  Monoalkylamines  Carbonyl compounds  Organic oxides  Organopnictogen compounds  Primary alcohols  
Molecular FrameworkAliphatic heteromonocyclic compounds
Substituents Hybrid peptide - Macrolactam - N-acyl-alpha amino acid or derivatives - Beta amino acid or derivatives - Alpha-amino acid or derivatives - Sulfuric acid - Fatty amide - Hydropyrimidine - 1,4,5,6-tetrahydropyrimidine - Fatty acyl - N-acyl-amine - Vinylogous amide - Organic sulfuric acid or derivatives - Amino acid or derivatives - Carboxamide group - Guanidine - Lactam - Carbonic acid derivative - Urea - Secondary carboxylic acid amide - Carboximidamide - Propargyl-type 1,3-dipolar organic compound - Organic 1,3-dipolar compound - Carboxylic acid derivative - Organoheterocyclic compound - Alkanolamine - Azacycle - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organic nitrogen compound - Organopnictogen compound - Primary aliphatic amine - Carbonyl group - Amine - Alcohol - Organonitrogen compound - Organooxygen compound - Primary alcohol - Primary amine - Aliphatic heteromonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as hybrid peptides. These are compounds containing at least two different types of amino acids (alpha, beta, gamma, delta) linked to each other through a peptide bond.
External Descriptors Not available
3D Structure
Interactive Chemical Structure Model





Mechanisms of Action
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Solution Calculators
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