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Uttronin A, a natural product derived from marine-derived fungi, is a unique polyketide with a molecular formula of C29H21O7. It exhibits potential anti-cancer properties, particularly in inhibiting the proliferation of human cancer cells in vitro. Its cytotoxic effects are notable on a range of cancer cell lines, especially those related to lung and colon cancers. Uttronin A disrupts microtubule dynamics in cancer cells, leading to cell cycle arrest and inducing apoptosis, making it a promising candidate for further development as a therapeutic agent for cancer treatment.

39941-51-0

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39941-51-0 Usage

Uses

Used in Pharmaceutical Industry:
Uttronin A is used as an anti-cancer agent for its ability to inhibit the proliferation of human cancer cells, particularly those associated with lung and colon cancers. Its mechanism of action involves disrupting microtubule dynamics, leading to cell cycle arrest and apoptosis.
Used in Cancer Research:
Uttronin A is used as a research tool for studying the effects of microtubule disruption on cancer cells and its potential as a therapeutic agent in cancer treatment. Its unique polyketide structure and molecular formula provide insights into the development of novel anti-cancer compounds.
Used in Drug Development:
Uttronin A is used as a lead compound in the development of new anti-cancer drugs. Its promising anti-cancer activities and cytotoxic effects on various cancer cell lines make it a valuable candidate for further research and development to improve cancer treatment options.

Check Digit Verification of cas no

The CAS Registry Mumber 39941-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,9,4 and 1 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 39941-51:
(7*3)+(6*9)+(5*9)+(4*4)+(3*1)+(2*5)+(1*1)=150
150 % 10 = 0
So 39941-51-0 is a valid CAS Registry Number.

39941-51-0 Well-known Company Product Price

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  • Sigma-Aldrich

  • (92056)  Degalactotigonin  analytical standard

  • 39941-51-0

  • 92056-10MG

  • 8,172.45CNY

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39941-51-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Desgalactotigonin

1.2 Other means of identification

Product number -
Other names DEGALACTOTIGONIN

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:39941-51-0 SDS

39941-51-0Upstream product

39941-51-0Downstream Products

39941-51-0Relevant academic research and scientific papers

Further Studies on Steroidal Glycosides from Bulbs, Roots and Leaves of Allium sativum L.

Matsuura, Hiromichi,Ushiroguchi, Tsuyoshi,Itakura, Yoichi,Fuwa, Toru

, p. 2741 - 2743 (2007/10/02)

A new furostanol glycoside (2), named sativoside-B1, was isolated from garlic, bulbs of Allium sativum L., along with proto-desgalactotigonin (3).The structure of 2 was established to be (25R)-26-O-β-D-glucopyranosyl-22-hydroxy-5α-furostane-3β,6β,26-triol 3-O-β-D-glucopyranosyl-(1->3)-O-β-D-glucopyranosyl-(1->2)-O-3)-O-β-D-glucopyranosyl-(1->4)-O-β-D-galactopyranoside.From roots of this plant, two new steroidal glycosides, named sativoside-R1 (16) and sativoside-R2 (15) were isolated and their structures were determined to be (25R)-26-O-β-D-glucopyranosyl-22-hydroxy-5α-furostane-3β,26-diol 3-O-β-D-glucopyranosyl-(1->3)-O-β-D-glucopyranosyl-(1->2)-O-3)>-O-β-D-glucopyranosyl-(1->4)-O-β-D-galactopyranosyde (16) and its corresponding spirostanol glycoside (15).Besides these glycosides, three known glycosides, 3, desgalactotigonin (13) and F-gitonin (14) were isolated and identified.In a glycoside fraction of the leaves of A. sativum, steroidal glycosides were not detected by thin layer chromatography analysis.

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