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30244-37-2

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  • Spiro[6,10-methanobenzocyclodecene-4(6H),2'-oxirane]-1,3,5,6,8,11,12-heptol,1,2,3,4a,5,7,8,11,12,12a-decahydro-9,12a,13,13-tetramethyl-,1,3,5,8,11,12-hexaacetate, (1S,2'R,3S,4aR,5S,6S,8S,11R,12R,12aS)

    Cas No: 30244-37-2

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  • Antimex Chemical Limied
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  • Spiro[6,10-methanobenzocyclodecene-4(6H),2'-oxirane]-1,3,5,6,8,11,12-heptol,1,2,3,4a,5,7,8,11,12,12a-decahydro-9,12a,13,13-tetramethyl-,1,3,5,8,11,12-hexaacetate, (1S,2'R,3S,4aR,5S,6S,8S,11R,12R,12aS)

    Cas No: 30244-37-2

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  • Hangzhou Fandachem Co.,Ltd
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  • Spiro[6,10-methanobenzocyclodecene-4(6H),2'-oxirane]-1,3,5,6,8,11,12-heptol,1,2,3,4a,5,7,8,11,12,12a-decahydro-9,12a,13,13-tetramethyl-,1,3,5,8,11,12-hexaacetate, (1S,2'R,3S,4aR,5S,6S,8S,11R,12R,12aS)

    Cas No: 30244-37-2

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  • shanghai Tauto Biotech Co., Ltd
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30244-37-2 Usage

General Description

1-HYDROXYBACCATIN I is a chemical compound that is a member of the taxane class of chemicals, which are known for their anti-cancer properties. It is derived from the Pacific yew tree and has been studied for its potential use in chemotherapy treatment for various types of cancer. Research has shown that 1-HYDROXYBACCATIN I has the ability to inhibit cell division and promote cell death, making it a promising candidate for cancer therapy. Its unique chemical structure allows it to target and disrupt the growth of cancer cells, making it a key focus of ongoing research into new cancer treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 30244-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,2,4 and 4 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 30244-37:
(7*3)+(6*0)+(5*2)+(4*4)+(3*4)+(2*3)+(1*7)=72
72 % 10 = 2
So 30244-37-2 is a valid CAS Registry Number.
InChI:InChI=1/C32H44O14/c1-14-21(41-15(2)33)12-32(39)28(46-20(7)38)26-30(10,22(42-16(3)34)11-23(43-17(4)35)31(26)13-40-31)27(45-19(6)37)25(44-18(5)36)24(14)29(32,8)9/h21-23,25-28,39H,11-13H2,1-10H3/t21-,22-,23-,25+,26-,27-,28-,30+,31-,32+/m0/s1

30244-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1β-hydroxybaccatin I

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

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

More Details:30244-37-2 SDS

30244-37-2Downstream Products

30244-37-2Relevant articles and documents

Taxanes from the roots of Taxus mairei

Shen, Ya-Ching,Chen, Ching-Yeu

, p. 1527 - 1533 (1997)

Extensive column chromatography of the ethanolic extracts from the roots of Taxus mairei and subsequent purification of taxanes by HPLC gave two derivatives of baccatin 1 and one derivative of taxchin. The structural assignments of the taxoids were based on their spectral data, including 2D NMR experiments and chemical correlation. X-ray crystallographic analysis of 1β-hydroxybaccatin 1 provided unambiguous characterization for the structures and relative stereochemistries of the other taxanes.

Bioactive taxoids from Japanese yew Taxus Cuspidata and taxol biosynthesis

Kobayashi, Jun'ichi,Shigemori, Hideyuki

, p. 1111 - 1133 (2007/10/03)

A series of new taxoids, named taxuspines A ~ H and J ~ Z (1 ~ 25), have been isolated together with 37 known taxoids (26 ~ 62) including taxol (42) from the Japanese yew Taxus cuspidata Sieb. et Zucc. These new taxoids possessed various skeletons containing 5/7/6, 6/10/6, 6/5/5/6, 6/8/6, or 6/12-membered ring systems. Among the new taxoids, some non-taxol-type compounds remarkably reduced CaCl2-induced depolymerization of microtubules, or increased cellular accumulation of vincristine in multidrug-resistant tumor cells as potent as verapamil. Here we describe our recent results on the isolation, structure elucidation, and bioactivity of these new and known taxoids as well as recent development of taxol biosynthesis.

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