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Sambutoxin, a toxic chemical compound produced by the bacterium Burkholderia thailandensis, is a member of the macrocyclic polyketides class. It exhibits potent cytotoxic effects on mammalian cells and is considered a virulence factor for the bacterium, aiding its competition with other microorganisms in the soil. Sambutoxin is also under investigation for its potential pharmaceutical applications, particularly in inhibiting the growth of cancer cells, and has been identified as a potential chemical warfare agent.

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  • 160047-56-3 Structure
  • Basic information

    1. Product Name: sambutoxin
    2. Synonyms: sambutoxin
    3. CAS NO:160047-56-3
    4. Molecular Formula: C28H39NO4
    5. Molecular Weight: 453.61356
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160047-56-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 592°C at 760 mmHg
    3. Flash Point: 311.8°C
    4. Appearance: /
    5. Density: 1.118g/cm3
    6. Vapor Pressure: 7.35E-15mmHg at 25°C
    7. Refractive Index: 1.564
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: sambutoxin(CAS DataBase Reference)
    11. NIST Chemistry Reference: sambutoxin(160047-56-3)
    12. EPA Substance Registry System: sambutoxin(160047-56-3)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 160047-56-3(Hazardous Substances Data)

160047-56-3 Usage

Uses

Used in Pharmaceutical Applications:
Sambutoxin is used as a potential anticancer agent for its ability to inhibit the growth of cancer cells in laboratory studies.
Used in Chemical Warfare Defense:
Sambutoxin is used as a target for the development of detection and neutralization methods due to its identification as a potential chemical warfare agent.

Check Digit Verification of cas no

The CAS Registry Mumber 160047-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,0,4 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 160047-56:
(8*1)+(7*6)+(6*0)+(5*0)+(4*4)+(3*7)+(2*5)+(1*6)=103
103 % 10 = 3
So 160047-56-3 is a valid CAS Registry Number.
InChI:InChI=1/C28H39NO4/c1-7-17(2)14-18(3)15-20(5)27-19(4)8-13-24(33-27)25-26(31)23(16-29(6)28(25)32)21-9-11-22(30)12-10-21/h9-12,15-19,24,27,30,32H,7-8,13-14H2,1-6H3/b20-15+/t17-,18+,19+,24-,27+/m0/s1

160047-56-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-[(2S,5R,6R)-6-[(E,4R,6S)-4,6-dimethyloct-2-en-2-yl]-5-methyloxan-2-yl]-4-hydroxy-5-(4-hydroxyphenyl)-1-methylpyridin-2-one

1.2 Other means of identification

Product number -
Other names Sambutoxin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:160047-56-3 SDS

160047-56-3Upstream product

160047-56-3Downstream Products

160047-56-3Relevant articles and documents

Biomimetic conversion of (-)-fusoxypyridone and (-)-oxysporidinone to (-)-sambutoxin: Further evidence for the structure of the tricyclic pyridone alkaloid, (-)-fusoxypyridone

Wijeratne, E.M. Kithsiri,Gunatilaka, A.A. Leslie

, p. 2327 - 2329 (2011)

Biomimetic-type reactions of the tricyclic pyridone alkaloid, (-)-fusoxypyridone [(-)-4,6′-anhydrooxysporidinone] (1), recently encountered in an endophytic strain of Fusarium oxysporum, and (-)-oxysporidinone (2) afforded (-)-sambutoxin (3) and an analog

Construction of 4-hydroxy-2-pyridinones. Total synthesis of (+)-sambutoxin

Williams, David R.,Turske, Regis A.

, p. 3217 - 3220 (2007/10/03)

(Matrix presented) Total synthesis of (+)-sambutoxin has been achieved, establishing the relative and absolute stereochemistry of the naturally occurring mycotoxin. Efforts feature methodology for enantiocontrolled construction of 1,3-anti-dimethyl arrays

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