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Ginkgolide K, a natural chemical compound derived from the Ginkgo biloba tree native to China, belongs to the class of diterpene lactones. It is recognized as a potent inhibitor of platelet-activating factor, a key mediator in inflammation and asthma. Ginkgolide K exhibits anti-inflammatory, antioxidant, and neuroprotective properties, positioning it as a promising candidate for the development of new drugs targeting neurological disorders, cardiovascular diseases, and inflammatory conditions. Furthermore, its ability to promote healthy blood circulation and improve cognitive function underscores its potential as a beneficial compound for human health.

153355-70-5

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153355-70-5 Usage

Uses

Used in Pharmaceutical Industry:
Ginkgolide K is used as a therapeutic agent for its anti-inflammatory, antioxidant, and neuroprotective properties, making it suitable for the treatment of neurological disorders, cardiovascular diseases, and inflammatory conditions.
Used in Health Supplements:
Ginkgolide K is used as a dietary supplement to promote healthy blood circulation and improve cognitive function, contributing to overall human health and well-being.
Used in Drug Development:
Ginkgolide K is utilized as a key compound in the development of new drugs targeting various health conditions, owing to its diverse range of therapeutic effects and potential for synergistic interactions with other compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 153355-70-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,3,5 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 153355-70:
(8*1)+(7*5)+(6*3)+(5*3)+(4*5)+(3*5)+(2*7)+(1*0)=125
125 % 10 = 5
So 153355-70-5 is a valid CAS Registry Number.

153355-70-5Downstream Products

153355-70-5Relevant academic research and scientific papers

A preparation method of Ginkgolide K

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Paragraph 0038-0039; 0044-0049; 0051; 0052, (2018/09/12)

The invention discloses a method for preparing ginkgolide K. The method includes the following steps: 1, ginkgolide B is dissolved into organic solvents to obtain a solution; 2, fluorinating agents are added into the solution obtained in the step 1 for conducting a dehydration reaction, and the ginkgolide K is obtained through separation and purification. The method for preparing the ginkgolide K is easy to operate; meanwhile, the high yield and the high purity are achieved, and convenience is brought to industrialization large-scale production. (please see the specification for the formula).

Ginkgolide K derivative and its preparation and use

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Paragraph 0056-0057, (2018/06/14)

The invention discloses a bilobalide K derivative and a preparation method and application thereof according to the formula I. Since structural modification is performed on bilobalide K, the bilobalide K derivative with higher water solubility and higher activity can be obtained and applied to prevention and treatment of cardiovascular and cerebrovascular diseases. Meanwhile, the bilobalide K derivative preparation process is facilitated and is adaptive to industrial production. (img file = 'DDA0000748217710000011.TIF' wi = '595' he = '515' /).

A concise synthesis of ginkgolide M, a minor component of a terpene trilactone fraction from Ginkgo biloba roots

Bolshakov, Sergei,Dzyuba, Sergei V.,Decatur, John,Nakanishi, Koji

, p. 429 - 431 (2008/09/19)

Ginkgolide M (GM), which is found only in the roots of the Ginkgo biloba tree and is an inhibitor of ligand-operated ion channels in the central nervous system, has been prepared in three steps from 10-benzylginkgolide C, an intermediate generated during the isolation and separation of ginkgolides from Ginkgo biloba leaf extract. The described synthetic sequence can be applied to access GM derivatives for biological studies.

Chemistry of the Ginkgolides, VI. - Preparation of 1,10-Dihydroxy- and 1,7,10-Trihydroxyginkgolide from 1,3,7,10-Tetrahydroxyginkgolide

Weinges, Klaus,Ruemmler, Matthias,Schick, Hartmut

, p. 1023 - 1028 (2007/10/02)

1,3,7,10-Tetrahydroxyginkgolide ("ginkgolide C", 1) which can be isolated in large quantities from the terpene fraction of Ginkgo leaves, can be converted into 1-(tert-butyldiphenylsilyloxy)-3,7,10-trihydroxyginkgolide (2) in 95percent yield. 2 was conver

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