2322-77-2 Usage
Description
Methoxydienone, also known as Max LMG, is a progestin-derived steroid that is structurally related to RU-486. It functions as an antiprogesterone, which means it can decrease estrogen-like effects. This unique property makes it a potential candidate for various applications in different industries.
Uses
Used in Pharmaceutical Industry:
Methoxydienone is used as a pharmaceutical agent for its antiprogesterone properties, which can help in managing and treating conditions related to hormonal imbalances and certain types of cancers. Its ability to decrease estrogen-like effects makes it a promising candidate for therapeutic applications.
Used in Contraceptive Applications:
In the contraceptive industry, Methoxydienone can be used as a component in the development of new contraceptive methods, thanks to its antiprogesterone activity. This could potentially offer an alternative option for individuals seeking different contraceptive choices.
Used in Hormonal Therapy:
Methoxydienone can be utilized in hormonal therapy for conditions such as endometriosis, where the reduction of estrogen-like effects can help alleviate symptoms and improve the patient's quality of life.
Used in Cancer Treatment:
Due to its structural relation to RU-486 and its antiprogesterone activity, Methoxydienone may also find applications in cancer treatment, particularly for hormone-sensitive tumors. Its potential to modulate oncological signaling pathways could contribute to the development of novel therapeutic strategies against various types of cancer.
Flammability and Explosibility
Nonflammable
Check Digit Verification of cas no
The CAS Registry Mumber 2322-77-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,2 and 2 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2322-77:
(6*2)+(5*3)+(4*2)+(3*2)+(2*7)+(1*7)=62
62 % 10 = 2
So 2322-77-2 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O2/c1-3-20-11-10-16-15-7-5-14(22-2)12-13(15)4-6-17(16)18(20)8-9-19(20)21/h5,16-18H,3-4,6-12H2,1-2H3/t16-,17-,18+,20+/m1/s1
2322-77-2Relevant articles and documents
SILICA GEL PROMOTED SELECTIVE HYDROLYSIS OF 3-METHOXY-2,5(10)-DIENE STEROIDS
Lui, Li-Gong,Zhang, Tong,Li, Zhen-Su
, p. 2999 - 3006 (2007/10/03)
Hydrolysis of 3-methoxy-2,5(10)-diene steroids (1a-c) via oxalic acid in the presence of silica gel was developed as a fast selective synthesis method toward corresponding 5(10)-en-3-ones (2a-c) in good yield (51-94percent).This also provided a new method for selective ketalisation of 17-keto over 3-keto (2c).
Aromatization of dl-3-methoxy-13β-ethylgona-2,5(10)-dien-17β-ol
Sharma,Chatterjee
, p. 158 - 159 (2007/10/02)
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Synthesis of gon-4-enes
-
, (2008/06/13)
1. A therapeutic composition having progestational activity comprising as active ingredient a 17-aliphatic carboxylic acid ester of 17α-ethynyl-18-methyl-19-nortestosterone and a pharmaceutical carrier for said compound.