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Gamma-tetrahydroartemisin (γ-THA) is a semi-synthetic derivative of the naturally occurring antimalarial compound artemisinin, which is isolated from the sweet wormwood plant (Artemisia annua). γ-THA is characterized by its unique peroxide bridge and endoperoxide linkage, which are crucial for its antimalarial activity. It is known for its ability to rapidly kill malaria parasites, particularly those resistant to other treatments. The chemical structure of γ-THA allows it to generate reactive oxygen species that damage the parasites' cellular components, leading to their death. γ-tetrahydroartemisin is a significant component in the development of artemisinin-based combination therapies (ACTs), which are the World Health Organization's recommended treatment for uncomplicated malaria cases. The use of γ-THA and other artemisinin derivatives has greatly improved the prognosis for malaria patients and has contributed to a decrease in malaria-related mortality.

86948-65-4

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86948-65-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86948-65-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,9,4 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 86948-65:
(7*8)+(6*6)+(5*9)+(4*4)+(3*8)+(2*6)+(1*5)=194
194 % 10 = 4
So 86948-65-4 is a valid CAS Registry Number.

86948-65-4Downstream Products

86948-65-4Relevant academic research and scientific papers

Biotransformation of 6α-santonin and 1,2-dihydro-α-santonin by Acremonium chrysogenum PTCC 5271 and Rhizomucor pusillus PTCC 5134

Gandomkar, Somayyeh,Habibi, Zohreh

, p. 59 - 63 (2015/01/08)

Biotransformation of 6α-santonin (1) and 1,2-dihyro-α-santonin (2) by two fungal strains Acremoniumchrysogenum (Cephalosporium chrysogenum) and Rhizomucor pusillus has been investigated for the firsttime. After 8 days of incubation of 1 by A. chrysogenum, four known metabolites including 1,2-dihydro-α-santonin (2) (30%), 8α-hydroxyl-α-santonin (3) (22%), 15-hydroxy-α-santonin (4) (15%) and 4,5-dihydro-α-santonin (5) (10%) were obtained. Incubation of 1 by R. pusillus afforded two metabolites 2 (45%) and 3(20%). Biotransformation of 1,2-dihyro-α-santonin by A. chrysogenum produced tetrahydro-α-santonin(6) with 52% yield and tetrahydroartemisin (7) with 33% yield. By R. pusillus, the yields of 6 and 7 were32% and 21%, respectively. The structures of the products were identified on the basis of spectroscopic data.

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