Shanghai Nianxing Industrial Co., Ltd
China
Product Name: Eurycomanone
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BioBioPha
China
Product Name: Eurycomanone
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Shanghai Jizhi Biochemical Technology Co., Ltd
China
Product Name: Eurycomanone
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DC Chemicals Limited
China
Product Name: Eurycomanone
Price: $650.0/100mg $1300.0/250mg $2600.0/1g
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ShangHai DC Chemicals Co.,Ltd
China
Product Name: Eurycomanone
Price: ￥Inquiry/1g
Purity: 98.9%
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84633-29-4

84633-29-4 structure

84633-29-4 structure

Name: Eurycomanone
Chemical Name: eurycomanone
CAS Number: 84633-29-4
Molecular Formula: C₂₀H₂₄O₉
Molecular Weight: 408.40
Catalog: Biochemical Plant extracts
Create Date: 2018-08-22 18:47:17
Modify Date: 2024-01-02 17:31:25
Eurycomanone could increases spermatogenesis by inhibiting the activity of phosphodiesterase and aromatase in steroidogenesis.

Name	eurycomanone
Synonyms	(1β,11α,12α,15β)-1,11,12,14,15-Pentahydroxy-11,20-epoxypicrasa-3,13(21)-diene-2,16-dione dihydrate pasakbumin-a EURYCOMANONE Picrasa-3,13(21)-diene-2,16-dione, 11,20-epoxy-1,11,12,14,15-pentahydroxy-, (1β,11α,12α,15β)-, hydrate (1:2)

Description	Eurycomanone could increases spermatogenesis by inhibiting the activity of phosphodiesterase and aromatase in steroidogenesis.
Related Catalog	Signaling Pathways >> Others >> Others Research Areas >> Endocrinology Natural Products >> Others
In Vitro	Eurycomanone (EN) significantly increased testosterone production dose-dependently at 0.1, 1.0 and 10.0 μM, but the two lower doses when combined with 3-isobutyl-1-methylxanthine (IBMX), the phosphodiesterase inhibitor were not significantly higher than EN or IBMX alone, except at a higher concentration. The molecular docking studies indicated EN and IBMX were binding at different sites of the enzyme. EN has no reversal of inhibition by aminoglutethimide, ketoconazole or nifedipine at the respective steroid oogenesis enzyme. The quassinoid was also non-responsive to the inhibition of oestrogen receptor by tamoxifen, but displayed improved for mestane inhibition of aromatase in reducing oestrogen production. The molecular docking studies further supported that EN and formestane bound to aromatase with similar orientations and free energy binding values[1].
References	[1]. Low BS, et al. Eurycomanone, the major quassinoid in Eurycoma longifolia root extract increases spermatogenesis by inhibiting the activity of phosphodiesterase and aromatase in steroidogenesis. J Ethnopharmacol. 2013 Aug 26;149(1):201-7.

Melting Point	273-285℃ (methanol ethyl ether )
Molecular Formula	C₂₀H₂₄O₉
Molecular Weight	408.40
PSA	172.21000
Storage condition	2-8℃

CHEMICAL IDENTIFICATION

RTECS NUMBER :: TJ7862500

CHEMICAL NAME :: Picrasa-3,13(21)-diene-2,16-dione, 11,2O-epoxy-1,11,12,14,15-pentahydroxy-, (1-beta,11- beta,12-alpha,15-beta)-, dihydrate

CAS REGISTRY NUMBER :: 84633-29-4

LAST UPDATED :: 199303

DATA ITEMS CITED :: 1

MOLECULAR FORMULA :: C20-H24-O9.2H2-O

MOLECULAR WEIGHT :: 444.48

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :: LD50 - Lethal dose, 50 percent kill

ROUTE OF EXPOSURE :: Intraperitoneal

SPECIES OBSERVED :: Rodent - mouse

DOSE/DURATION :: 18900 ug/kg

TOXIC EFFECTS :: Details of toxic effects not reported other than lethal dose value

REFERENCE :: EJMCA5 European Journal of Medicinal Chemistry--Chimie Therapeutique. (Editions Scientifiques Elsevier, 29 rue Buffon, F-75005, Paris, France) V.9- 1974- Volume(issue)/page/year: 26,345,1991

Precursor 0
DownStream 1
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