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Taxinine J, a complex natural product from the taxine family, is derived from Taxus plants. It features a tetracyclic core with multiple oxygen-containing functional groups, which contributes to its unique chemical structure and potent cytotoxic activity against cancer cell lines. Taxinine J is known to interfere with microtubule dynamics, a critical process in cell division, making it a promising candidate for the development of new anti-cancer drugs.

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  • 18457-46-0 Structure
  • Basic information

    1. Product Name: Taxinine J
    2. Synonyms: Taxinine J;Cuspidatin C;Taxinin J
    3. CAS NO:18457-46-0
    4. Molecular Formula: C37H46O10
    5. Molecular Weight: 650.75514
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 18457-46-0.mol
  • Chemical Properties

    1. Melting Point: 249-251℃
    2. Boiling Point: 673.8°Cat760mmHg
    3. Flash Point: 273.8°C
    4. Appearance: /
    5. Density: 1.21g/cm3
    6. Vapor Pressure: 5.17E-18mmHg at 25°C
    7. Refractive Index: 1.553
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: Taxinine J(CAS DataBase Reference)
    11. NIST Chemistry Reference: Taxinine J(18457-46-0)
    12. EPA Substance Registry System: Taxinine J(18457-46-0)
  • 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: 18457-46-0(Hazardous Substances Data)

18457-46-0 Usage

Uses

Used in Pharmaceutical Industry:
Taxinine J is used as a potential lead compound for the development of new anti-cancer drugs due to its potent cytotoxic activity against various cancer cell lines. Its ability to interfere with microtubule dynamics makes it a valuable asset in the fight against cancer.
Used in Cancer Research:
Taxinine J is utilized as a research tool to study the effects of microtubule dynamics on cell division and the development of cancer. Understanding its mechanism of action can provide insights into the development of novel therapeutic strategies targeting cancer cells.
Used in Drug Synthesis:
Due to its complex and unique chemical structure, Taxinine J presents a challenging target for chemical synthesis. Researchers are interested in developing efficient synthetic routes to produce this compound, which can facilitate its use in drug development and cancer treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 18457-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,4,5 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18457-46:
(7*1)+(6*8)+(5*4)+(4*5)+(3*7)+(2*4)+(1*6)=130
130 % 10 = 0
So 18457-46-0 is a valid CAS Registry Number.
InChI:InChI=1/C37H46O10/c1-20-28-17-27-18-29(43-22(3)38)21(2)33(36(27,7)8)34(45-24(5)40)35(46-25(6)41)37(28,9)31(44-23(4)39)19-30(20)47-32(42)16-15-26-13-11-10-12-14-26/h10-16,27-31,34-35H,1,17-19H2,2-9H3/b16-15+

18457-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Cuspidatin C

1.2 Other means of identification

Product number -
Other names -

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:18457-46-0 SDS

18457-46-0Upstream product

18457-46-0Downstream Products

18457-46-0Relevant articles and documents

New taxanes from the needles of Taxus canadensis

Zhang,Sauriol,Mamer,Zamir, Lolita O.

, p. 929 - 933 (2007/10/03)

Nine minor taxanes were identified for the first time in the Canadian yew needles. Four of these metabolites are new: 5-epi-cinnamoylcanadensene (1), 2,9,10,13-tetraacetoxy-20-cinnamoyloxy-taxa-4(5),11(12)-diene (2), 2'-acetyl-epi-taxol (3), and 9-deacety

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