DHQHS 2
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DHQHS 2
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CAS No:
71939-50-9
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Formula:
C15H24O5
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Chemical Name:
DHQHS 2
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Synonyms:
Dihydroartemisinin 71939-50-9;Dihydroartemisinin (3R,5aS,6R,8aS,9R,10S,12R,12aR)-Decahydro-3,6,9-trimethyl-3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10-ol;]hexadecan-6-ol;Dihydroarteminisin;Dihydroartemisin;(3R,5aS,6R,8aS,9R,10S,12R,12aR)-Decahydro-3,6,9-trimethyl- 3,12-epoxy-12H-pyrano[4,3-j]-1,2-benzodioxepin-10-ol;Alaxin;b-Dihydroartemisinin
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CAS No:
Description
Dihydroartemisinin is a potent anti-malaria agent.
White Solid
ChEBI: Artenimol is an artemisinin derivative.
DHQHS 2 Basic Attributes
284.35
284.35
DTXSID5045962
White to Almost white
P01BF05|P - Antiparasitic products, insecticides and repellents
29329990
Characteristics
57.15000
2.18670
solid
1.24
144-149°C
375.6±42.0 °C(Predicted)
181.0±27.9 °C
1.543
2-8°C
12.61±0.70(Predicted)
Inert atmosphere,2-8°C
Safety Information
NONH for all modes of transport
2
22-24/25
KD4165550
|Warning|H242 (100%): Heating may cause a fire [Danger Self-reactive substances and mixtures; Organic peroxides]|P210, P220, P234, P273, P280, P370+P378, P391, P403+P235, P411, P420, and P501|Aggregated GHS information provided by 2 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Drug Information
Eurartesim is indicated for the treatment of uncomplicated Plasmodium falciparum malaria in adults, children and infants 6 months and over and weighing 5 kg or more.Consideration should be given to official guidance on the appropriate use of antimalarial agents.|Treatment of uncomplicated malaria caused by Plasmodium falciparum
Agents used in the treatment of malaria. They are usually classified on the basis of their action against plasmodia at different stages in their life cycle in the human. (From AMA, Drug Evaluations Annual, 1992, p1585) (See all compounds classified as Antimalarials.)
3alpha-hydroxydeoxydihydroartemisinin
DHQHS 2 Use and Manufacturing
LiBHEtSodium borohydride (2.02 g, 53.19 mmol) was added in five portions within 30 minutes to the solution of artemisinin (5 g, 17.73 mmol) in methanol (60 mL) under 5. The reaction mixture was kept stirring for approximately 1h at 0–5, the acetic acid was added to adjust PH =7.0. The reaction solution was concentrated to remove most of methanol, diluted with cold water (60 mL) and stirred for 15 min at room temperature. The precipitate was collected, washed with water (20 mL*3) and dried to afford product as white solid, 4.51 g, yield: 89.57percent.Dihydroartemisinin (DHA) synthesis:Artemisinin (5.0 g, 18 mmol) was dissolved in anhydrous methanol (120 mL).It was placed in an ice water bath, and NaBH4 (1.0 g, 27 mmol) was added portionwise with stirring, and was added over 20 min. The reaction is about 2 hours, and the reaction is completed.Adjust pH 6-7 with glacial acetic acid and distill off most of the methanol.Stir with water for 15 min, filter and collect the precipitate.Wash three times with water, dry, Obtained as a white solid (3.0 g, 59percent).
The main metabolite of Artemisinin, Arteether, Artemether, Artesunate. An active antimalarial metabolite
Human drugs -> Eurartesim -> EMA Drug Category|Antiprotozoals -> Human pharmacotherapeutic group|Human drugs -> Rare disease (orphan)|Human Drugs -> EU pediatric investigation plans
Drug Function and Efficacy
It has a strong killing effect on the asexual body of malarial parasites and can quickly kill malarial parasites, thereby quickly controlling symptoms.
Registered Holders
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Zhejiang NHU Company Ltd.
Active
China
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Guilin Pharmaceutical Co., Ltd.
Active
China
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China Resources Sanjiu (Youyang) Pharmaceutical Co., Ltd.
Active
China
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