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(16R)-2α,5α-Epoxy-16-formyl-1,2-dihydroakuammilan-17-oic acid methyl ester is a complex chemical compound derived from akuammilan alkaloids, which are naturally occurring compounds found in the plant Vinca rosea. This specific compound is characterized by its 16R stereoisomer configuration, a 2α,5α-epoxy group, a formyl group at the 16th position, and a carboxylic acid group at the 17th position. The presence of these functional groups endows the compound with unique chemical and biological properties, making it a promising candidate for further research and development in various pharmacological applications.

20045-06-1

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20045-06-1 Usage

Uses

Used in Pharmaceutical Industry:
(16R)-2α,5α-Epoxy-16-formyl-1,2-dihydroakuammilan-17-oic acid methyl ester is used as a potential therapeutic agent for various diseases due to its pharmacological activities. Its unique chemical structure allows it to interact with biological targets, making it a promising candidate for the development of new drugs.
Used in Anticancer Applications:
(16R)-2α,5α-Epoxy-16-formyl-1,2-dihydroakuammilan-17-oic acid methyl ester is used as an anticancer agent, leveraging its potential to target and inhibit the growth of cancer cells. Its unique chemical properties may allow it to modulate signaling pathways and disrupt the processes that contribute to tumor growth and progression.
Used in Anti-malarial Applications:
(16R)-2α,5α-Epoxy-16-formyl-1,2-dihydroakuammilan-17-oic acid methyl ester is used as an anti-malarial agent, where its unique chemical structure may help in targeting and inhibiting the Plasmodium parasites responsible for malaria, offering a potential new approach to treating this disease.
Used in Anti-inflammatory Applications:
(16R)-2α,5α-Epoxy-16-formyl-1,2-dihydroakuammilan-17-oic acid methyl ester is used as an anti-inflammatory agent, potentially modulating the immune response and reducing inflammation. Its unique functional groups may allow it to interact with specific biological targets, providing a new avenue for the treatment of inflammatory conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 20045-06-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,4 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20045-06:
(7*2)+(6*0)+(5*0)+(4*4)+(3*5)+(2*0)+(1*6)=51
51 % 10 = 1
So 20045-06-1 is a valid CAS Registry Number.

20045-06-1Upstream product

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