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(2R)-Pterosin B, a naturally occurring sesquiterpene compound, is a member of the 'pterosins' family found predominantly in the bracken fern. Known for its cytotoxic, antifungal, and antibacterial properties, it has garnered significant attention for its potential medical applications. However, its consumption in high amounts is considered potentially carcinogenic for humans due to its cytotoxic nature, which can damage or kill cells.

34175-96-7

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34175-96-7 Usage

Uses

Used in Pharmaceutical Industry:
(2R)-Pterosin B is used as a pharmaceutical agent for its cytotoxic properties, which can be harnessed to target and kill cancer cells. Its potential as an anticancer compound is under extensive research, particularly for its ability to inhibit the growth of various types of cancer cells.
Used in Antimicrobial Applications:
(2R)-Pterosin B is used as an antimicrobial agent for its antifungal and antibacterial properties, making it a candidate for the development of new antibiotics and antifungal medications to combat drug-resistant infections.
Used in Research and Development:
(2R)-Pterosin B is utilized in research and development for its potential applications in medicine and its impact on human and animal health. Ongoing studies aim to understand its mechanisms of action, optimize its therapeutic potential, and mitigate its potential carcinogenic effects when consumed in high amounts.

Check Digit Verification of cas no

The CAS Registry Mumber 34175-96-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,1,7 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 34175-96:
(7*3)+(6*4)+(5*1)+(4*7)+(3*5)+(2*9)+(1*6)=117
117 % 10 = 7
So 34175-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H18O2/c1-8-6-11-7-9(2)14(16)13(11)10(3)12(8)4-5-15/h6,9,15H,4-5,7H2,1-3H3/t9-/m1/s1

34175-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydro-1H-inden-1-one

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:34175-96-7 SDS

34175-96-7Relevant academic research and scientific papers

Cytotoxic diterpenoids and sesquiterpenoids from Pteris multifida

Ge, Xin,Ye, Guan,Li, Ping,Tang, Wen-Jie,Gao, Jin-Li,Zhao, Wei-Min

, p. 227 - 231 (2008)

Three new ent-kaurane diterpenoids, named pterokaurane M1-M 3 (1-3) and three new C14 pterosin-sesquiterpenoids, named multifidoside A-C (4-6), along with 18 known compounds, were isolated from the whole plants of Pteris multifida. The structures of 1-6 were established using spectroscopic methods, including extensive 2D NMR and CD analyses. Compounds 4 and 5 showed cytotoxicity against the HepG2 tumor cell line with IC50 values of less than 10 μM.

PTAQUILOSIDE, A POTENT CARCINOGEN ISOLATED FROM BRACKEN FERN PTERIDIUM AQUILINUM VAR. LATIUSCULUM: STRUCTURE ELUCIDATION BASED ON CHEMICAL AND SPECTRAL EVIDENCE, AND REACTIONS WITH AMINO ACIDS, NUCLEOSIDES, AND NUCLEOTIDES

Ojika, Makoto,Wakamatsu, Kazumasa,Niwa, Haruki,Yamada, Kiyoyuki

, p. 5261 - 5274 (2007/10/02)

The structure of ptaquiloside (I), a potent carcinogenic compound isolated from bracken fern, Pteridium aquilinum var. latiusculum has been elucidated on the basis of chemical and spectral evidence.The dienone 3 generated from 1 under alkaline conditions was shown to be a strong alkylating agent.For the purpose of obtaining the preliminary information on chemical modification of biopolymers such as proteins and DNA with the dienone 3, reactions of 3 with amino acids, nucleosides, and nucleotides have been carried out and the alkylated products have been characterized.

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