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1-methyl-5α-androst-1-ene-3,17-dione is a synthetic steroid compound that belongs to the androstane family. It is characterized by the presence of a methyl group at the 1st carbon, a double bond between the 1st and 2nd carbons, and a ketone group at both the 3rd and 17th carbons. This chemical structure is derived from the naturally occurring androstane skeleton, which is a key component in many endogenous and exogenous steroids. The compound has potential applications in pharmaceuticals and sports performance enhancement, although its use is often regulated due to its anabolic and androgenic effects. It is important to note that the use of such substances without proper medical supervision can lead to various health risks and is subject to legal restrictions in many jurisdictions.

1424-01-7

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1424-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1424-01-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1424-01:
(6*1)+(5*4)+(4*2)+(3*4)+(2*0)+(1*1)=47
47 % 10 = 7
So 1424-01-7 is a valid CAS Registry Number.

1424-01-7Upstream product

1424-01-7Downstream Products

1424-01-7Relevant academic research and scientific papers

Aspergillus Niger-mediated biotransformation of methenolone enanthate, and immunomodulatory activity of its transformed products

Hussain, Zahid,Dastagir, Nida,Hussain, Shabbir,Jabeen, Almas,Zafar, Salman,Malik, Rizwana,Bano, Saira,Wajid, Abdul,Choudhary, M. Iqbal

, p. 68 - 73 (2016)

Two fungal cultures Aspergillus Niger and Cunninghamella blakesleeana were used for the biotransformation of methenolone enanthate (1). Biotransformation with A. Niger led to the synthesis of three new (2-4), and three known (5-7) metabolites, while fermentation with C. blakesleeana yielded metabolite 6. Substrate 1 and the resulting metabolites were evaluated for their immunomodulatory activities. Substrate 1 was found to be inactive, while metabolites 2 and 3 showed a potent inhibition of ROS generation by whole blood (IC50 = 8.60 and 7.05 μg/mL), as well as from isolated polymorphonuclear leukocytes (PMNs) (IC50 = 14.0 and 4.70 μg/mL), respectively. Moreover, compound 3 (34.21%) moderately inhibited the production of TNF-α, whereas 2 (88.63%) showed a potent inhibition of TNF-α produced by the THP-1 cells. These activities indicated immunomodulatory potential of compounds 2 and 3. All products were found to be non-toxic to 3T3 mouse fibroblast cells.

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