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567-75-9

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567-75-9 Usage

General Description

Leptospermone is a natural chemical compound found in the essential oils of certain plant species, such as the Leptospermum scoparium, commonly known as manuka. It is a member of the class of organic compounds known as prenylflavonoids, and is known for its antimicrobial and antioxidant properties. Leptospermone has been the subject of scientific research for its potential to treat various health conditions, including bacterial infections and cancer. Its unique chemical structure and biological activity make it a promising candidate for the development of new antimicrobial and antioxidant agents for medical and cosmetic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 567-75-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 567-75:
(5*5)+(4*6)+(3*7)+(2*7)+(1*5)=89
89 % 10 = 9
So 567-75-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H22O4/c1-8(2)7-9(16)10-11(17)14(3,4)13(19)15(5,6)12(10)18/h8,10H,7H2,1-6H3

567-75-9SDS

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 2,2,4,4-tetramethyl-6-(3-methylbutanoyl)cyclohexane-1,3,5-trione

1.2 Other means of identification

Product number -
Other names 6-isovaleryl-2,2,4,4-tetramethyl-cyclohexane-1,3,5-trione

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:567-75-9 SDS

567-75-9Relevant articles and documents

Rhodomentosones A and B: Two Pairs of Enantiomeric Phloroglucinol Trimers from Rhodomyrtus tomentosa and Their Asymmetric Biomimetic Synthesis

Bai, Yang-Ting-Zhi,Deng, Lu-Ming,Hu, Li-Jun,Huang, Xiao-Jun,Jiang, Ren-Wang,Li, Chuang-Chuang,Li, Yao-Lan,Qin, Guan-Qiu,Song, Qiao-Yun,Su, Jun-Cheng,Tang, Wei,Wang, Jie,Wang, Ying,Ye, Wen-Cai

, p. 4499 - 4504 (2021/06/28)

Rhodomentosones A and B (1 and 2), two pairs of novel enantiomeric phloroglucinol trimers featuring a unique 6/5/5/6/5/5/6-fused ring system were isolated from Rhodomyrtus tomentosa. Their structures with absolute configurations were elucidated by NMR spe

Synthesis and P-glycoprotein induction activity of colupulone analogs

Bharate, Jaideep B.,Batarseh, Yazan S.,Wani, Abubakar,Sharma, Sadhana,Vishwakarma, Ram A.,Kaddoumi, Amal,Kumar, Ajay,Bharate, Sandip B.

, p. 5488 - 5496 (2015/05/20)

Brain amyloid-beta (Aβ) plaques are one of the primary hallmarks associated with Alzheimer's disease (AD) pathology. Efflux pump proteins located at the blood-brain barrier (BBB) have been reported to play an important role in the clearance of brain Aβ, among which the P-glycoprotein (P-gp) efflux transporter pump has been shown to play a crucial role. Thus, P-gp has been considered as a potential therapeutic target for treatment of AD. Colupulone, a prenylated phloroglucinol isolated from Humulus lupulus, is known to activate pregnane-X-receptor (PXR), which is a nuclear receptor controlling P-gp expression. In the present work, we aimed to synthesize and identify analogs of colupulone that are potent P-gp inducer(s) with an ability to enhance Aβ transport across the BBB. A series of colupulone analogs were synthesized by modifications at both prenyl as well as acyl domains. All compounds were screened for P-gp induction activity using a rhodamine 123 based efflux assay in the P-gp overexpressing human adenocarcinoma LS-180 cells, wherein all compounds showed significant P-gp induction activity at 5 μM. In the western blot studies in LS-180 cells, compounds 3k and 5f were able to induce P-gp as well as LRP1 at 1 μM. The effect of compounds on the Aβ uptake and transport was then evaluated. Among all tested compounds, diprenylated acyl phloroglucinol 5f displayed a significant increase (29%) in Aβ transport across bEnd3 cells grown on inserts as a BBB model. The results presented here suggest the potential of this scaffold to enhance clearance of brain Aβ across the BBB and thus its promise for development as a potential anti-Alzheimer agent.

β-triketones from Myrtaceae: Isoleptospermone from Leptospermum scoparium and papuanone from Corymbia dallachiana

Van Klink, John W.,Brophy, Joseph J.,Perry, Nigel B.,Weavers, Rex T.

, p. 487 - 489 (2007/10/03)

Naturally occurring β-triketones, isoleptospermone [3, 5-hydroxy-4-(2- methyl-1-oxopentyl)-2,2,6,6-tetramethyl-4-cyclohexene-1,3-dione) from Leptospermum scoparium] and papuanone [6, 5-hydroxy-4-(1-oxohexyl)-2,2,6,6- tetramethyl-4-cyclohexene-1,3-dione fr

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