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4H-1-Benzopyran-4-one,8-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-2,3-dihydro-5,7-dihydroxy-6-(3-methyl-2-buten-1-yl)-2-phenyl-,(2S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

116107-13-2

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116107-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 116107-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,0 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 116107-13:
(8*1)+(7*1)+(6*6)+(5*1)+(4*0)+(3*7)+(2*1)+(1*3)=82
82 % 10 = 2
So 116107-13-2 is a valid CAS Registry Number.

116107-13-2SDS

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 isoallorottlerin

1.2 Other means of identification

Product number -
Other names 8-(3-Acetyl-2,4,6-trihydroxy-5-methyl-benzyl)-5,7-dihydroxy-6-(3-methyl-but-2-enyl)-2-phenyl-chroman-4-one

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:116107-13-2 SDS

116107-13-2Upstream product

116107-13-2Downstream Products

116107-13-2Relevant academic research and scientific papers

Semisynthesis of mallotus B from rottlerin: Evaluation of cytotoxicity and apoptosis-inducing activity

Jain, Shreyans K.,Pathania, Anup S.,Meena, Samdarshi,Sharma, Rajni,Sharma, Ashok,Singh, Baljinder,Gupta, Bishan D.,Bhushan, Shashi,Bharate, Sandip B.,Vishwakarma, Ram A.

, p. 1724 - 1730 (2013/10/22)

Mallotus B (2d) is a prenylated dimeric phloroglucinol compound isolated from Mallotus philippensis. There have been no reports on the synthesis or biological activity of this compound. In the present paper, a semisynthetic preparation of mallotus B is reported via base-mediated intramolecular rearrangement of rottlerin (1), which is one of the major constituents of M. philippensis. The homodimer rottlerone was also formed as one of the products of this base-mediated intramolecular reaction. Rottlerin (1), along with rottlerone (2c) and mallotus B (2d), was evaluated for cytotoxicity against a panel of cancer cell lines including HEPG2, Colo205, MIAPaCa-2, PC-3, and HL-60 cells. Mallotus B (2d) displayed cytotoxicity for MIAPaCa-2 and HL-60 cells with IC50 values of 9 and 16 μM, respectively. Microscopic studies in HL-60 cells indicated that mallotus B (2d) induces cell cycle arrest at the G1 phase and causes defective cell division. It also induces apoptosis, as evidenced by distinct changes in cell morphology.

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