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(2beta,9alpha,11beta,13R,14xi,20xi)-hetisan-2,11,13-triol is a complex chemical compound belonging to the hetisane group, which is a class of naturally occurring compounds found in plants and marine organisms. Its unique molecular structure, composed of carbon, hydrogen, and oxygen atoms, endows it with distinctive properties and potential biological activities. The triterpenoid nature of (2beta,9alpha,11beta,13R,14xi,20xi)-hetisan-2,11,13-triol suggests that it may possess pharmacological properties, although further research is necessary to confirm its exact biological functions and applications.

10089-23-3

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10089-23-3 Usage

Uses

Used in Pharmaceutical Research:
(2beta,9alpha,11beta,13R,14xi,20xi)-hetisan-2,11,13-triol is used as a subject of pharmaceutical research for its potential anti-inflammatory, anti-cancer, or other medicinal properties. Its unique structure and potential biological activities make it a promising candidate for further investigation and development in the fields of chemistry and medicine.
Used in Drug Discovery:
In the Drug Discovery industry, (2beta,9alpha,11beta,13R,14xi,20xi)-hetisan-2,11,13-triol is used as a lead compound for the development of new drugs. Its complex molecular structure and potential pharmacological properties make it a valuable asset for exploring novel therapeutic agents and treatments.
Used in Chemical Research:
(2beta,9alpha,11beta,13R,14xi,20xi)-hetisan-2,11,13-triol is utilized in chemical research to study its unique molecular structure and the relationship between its chemical composition and potential biological activities. This research can contribute to a better understanding of the properties of hetisane compounds and their potential applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 10089-23-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,8 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10089-23:
(7*1)+(6*0)+(5*0)+(4*8)+(3*9)+(2*2)+(1*3)=73
73 % 10 = 3
So 10089-23-3 is a valid CAS Registry Number.

10089-23-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name HETISINE

1.2 Other means of identification

Product number -
Other names Hetisan-2,11,13-triol

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:10089-23-3 SDS

10089-23-3Upstream product

10089-23-3Relevant academic research and scientific papers

Diterpenoid alkaloids and flavonoids from Delphinium trichophorum

Lin, Chao-Zhan,Zhao, Zhong-Xiang,Xie, Si-Min,Mao, Ju-Hua,Zhu, Chen-Chen,Li, Xiao-Hui,Bairi, Zeren-Dawa,Kangsa, Suolang-Qimei,Dun, Zhu,Xiong, Tian-Qin,Wu, Ai-Zhi

, p. 88 - 95 (2014)

Five hetisane-type C20-diterpenoid alkaloids, trichodelphinines A-E, one delnudine-type C20-diterpenoid alkaloid, trichodelphinine F and three known flavonoids, quercetin, quercetin 3-O-β-d-glucopyranoside, and quercetin 3-O-β-d-glucopyranoside-7-O-α-l-arabinopyranoside, were isolated from whole plants of Delphinium trichophorum Franch. Their structures were elucidated on the basis of extensive spectroscopic analysis, including HSQC, HMBC, 1H-1H COSY, NOESY and X-ray crystallographic analysis, and from chemical evidence. The cytotoxic activities of the diterpenoid alkaloids were evaluated using the MTT method, and the IC 50 values of their cytotoxicity against A549 cancer cells ranged from 12.03 to 52.79 μM.2013 Elsevier Ltd. All rights reserved.

(13)C NMR SPECTROSCOPY OF SOME HETISINE SUBTYPE C20-DITERPENOID ALKALOIDS AND THEIR DERIVATIVES

Gonzalez, A. G.,Fuente De La, G.,Reina, M.,Diaz, R.,Timon, I.

, p. 1971 - 1974 (2007/10/02)

The 13C NMR spectra of the diterpenoid alkaloids hetisine; hetisinone; 13-acetylhetisinone; cardiopetamine, and 15-acetylcardiopetamine, as well as certain of their derivatives, were obtained in the Fourier mode at 50.32 MHz.With the aid of proton decoupling techniques, SFORD and SFDS, and chemical shift comparisons, selfconsistent assignments of nearly all the resonance have been made.

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