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Actinomycin V

Base Information
  • Chemical Name:Actinomycin V
  • CAS No.:18865-48-0
  • Molecular Formula:C62H84N12O17
  • Molecular Weight:1269.40
  • Hs Code.:
  • European Community (EC) Number:242-636-3
  • Wikidata:Q105015625
  • ChEMBL ID:CHEMBL4287110
  • Mol file:18865-48-0.mol
Actinomycin V

Synonyms:actinomycin V

Suppliers and Price of Actinomycin V
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • 5''-Deoxy-5''-(methylthio)adenosine-d3
  • 2.5mg
  • $ 185.00
  • Medical Isotopes, Inc.
  • 5??-Deoxy-5??-(methylthio)adenosine-d3
  • 25 mg
  • $ 2200.00
  • Medical Isotopes, Inc.
  • 5??-Deoxy-5??-(methylthio)adenosine-d3
  • 2.5 mg
  • $ 650.00
  • Cayman Chemical
  • 5''-Deoxy-5''-methylthioadenosine-d3
  • 1mg
  • $ 45.00
  • American Custom Chemicals Corporation
  • ACTINOMYCIN V 95.00%
  • 10MG
  • $ 550.00
  • Adipogen Life Sciences
  • ActinomycinX2 ≥98%(HPLC)
  • 1 mg
  • $ 90.00
Total 49 raw suppliers
Chemical Property of Actinomycin V
Chemical Property:
  • Vapor Pressure:0mmHg at 25°C 
  • Melting Point:250°C 
  • Refractive Index:1.661 
  • Boiling Point:1411.4 °C at 760 mmHg 
  • Flash Point:807.4 °C 
  • PSA:377.05000 
  • Density:1.44 g/cm3 
  • LogP:1.55260 
  • Storage Temp.:2-8°C 
  • Solubility.:DMSO (Slightly), Methanol (Slightly, Heated) 
  • XLogP3:2.8
  • Hydrogen Bond Donor Count:5
  • Hydrogen Bond Acceptor Count:19
  • Rotatable Bond Count:8
  • Exact Mass:1268.60773926
  • Heavy Atom Count:91
  • Complexity:3120
Purity/Quality:

99%, *data from raw suppliers

5''-Deoxy-5''-(methylthio)adenosine-d3 *data from reagent suppliers

Safty Information:
  • Pictogram(s): VeryT+ 
  • Hazard Codes:T+ 
  • Statements: 26/27/28-63 
  • Safety Statements: 22-36/37/39-45 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1C(C(=O)NC(C(=O)N2CCCC2C(=O)N(CC(=O)N(C(C(=O)O1)C(C)C)C)C)C(C)C)NC(=O)C3=C4C(=C(C=C3)C)OC5=C(C(=O)C(=C(C5=N4)C(=O)NC6C(OC(=O)C(N(C(=O)CN(C(=O)C7CC(=O)CN7C(=O)C(NC6=O)C(C)C)C)C)C(C)C)C)N)C
  • Isomeric SMILES:C[C@@H]1[C@@H](C(=O)N[C@@H](C(=O)N2CCC[C@H]2C(=O)N(CC(=O)N([C@H](C(=O)O1)C(C)C)C)C)C(C)C)NC(=O)C3=C4C(=C(C=C3)C)OC5=C(C(=O)C(=C(C5=N4)C(=O)N[C@H]6[C@H](OC(=O)[C@@H](N(C(=O)CN(C(=O)[C@@H]7CC(=O)CN7C(=O)[C@H](NC6=O)C(C)C)C)C)C(C)C)C)N)C
  • Uses Labelled 5''-Deoxy-5''-(methylthio)adenosine (D242600). 5′-Deoxy-5′-(methylthio)adenosine (Methylthioadenosine) may be used as a substrate to study the specificity and kinetics of 5′-methylthioadenosinephosphorylase (MTAP) (EC2.4.2.28), a tumor suppressor gene expressed enzyme that supports the S-adenosylmethionine (AdoMet) and methionine salvage pathways. Methylthioadenosine is used in studies on bacterial quorum sensing pathways that envolve enzymes such as 5′-Methylthioadenosine/S-adenosylhomocysteine nucleosidase (MTAN).
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