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11-{[3,28-dioxolup-20(29)-en-28-yl]amino}undecanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

150840-33-8

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150840-33-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150840-33-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,8,4 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 150840-33:
(8*1)+(7*5)+(6*0)+(5*8)+(4*4)+(3*0)+(2*3)+(1*3)=108
108 % 10 = 8
So 150840-33-8 is a valid CAS Registry Number.

150840-33-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 11-[[(1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bR)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a-carbonyl]amino]undecanoic acid

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:150840-33-8 SDS

150840-33-8Downstream Products

150840-33-8Relevant academic research and scientific papers

Synthesis of betulonic acid derivatives containing amino-acid fragments

Petrenko,Elantseva,Petukhova,Shakirov,Shul'ts,Tolstikov

, p. 331 - 339 (2007/10/03)

New derivatives of betulonic acid containing on C-28 fragments of amino acids or their methyl esters were prepared as potential biologically active agents.

Betulinic acid derivatives: A new class of human immunodeficiency virus type 1 specific inhibitors with a new mode of action

Evers, Michel,Poujade, Christèle,Soler, Fran?oise,Ribeill, Yves,James, Claude,Lelièvre, Yves,Gueguen, Jean-Christophe,Reisdorf, Daniel,Morize, Isabelle,Pauwels, Rudi,De Clercq, Erik,Hénin, Yvette,Bousseau, Anne,Mayaux, Jean-Fran?ois,Le Pecq, Jean-Bernard,Dereu, Norbert

, p. 1056 - 1068 (2007/10/03)

A series of ω-undecanoic amides of lup-20(29)-en-28-oic acid derivatives were synthesized and evaluated for activity in CEM 4 and MT-4 cell cultures against human immunodeficiency virus type 1 (HIV-1) strain III(B)/LAI. The potent HIV inhibitors which emerged, compounds 5a, 16a, and 17b, were all derivatives of betulinic acid (3β-hydroxylup-20(29)-en-28-oic acid). No activity was found against HIV-2 strain ROD. Compound 5a showed no inhibition of HIV-1 reverse transcriptase activity with poly(C)·oligo(dG) as template/primer, nor did it inhibit HIV-1 protease. Additional mechanistic studies revealed that this class of compounds interfere with HIV-1 entry in the cells at a postbinding step.

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