Welcome to LookChem.com Sign In|Join Free
  • or
Monoginol A is a naturally occurring chemical compound that belongs to the class of diterpenoids, specifically within the family of labdane-type diterpenes. It is primarily found in the seeds of the Monodora myristica plant, which is native to tropical regions of Africa. Monoginol A has gained attention for its potential bioactivity, including anti-inflammatory and antimicrobial properties. Research on Monoginol A is ongoing, with studies exploring its effects on various biological systems and its potential applications in medicine and pharmacology. The compound's structure and functional groups contribute to its unique properties, making it a subject of interest for further chemical and pharmacological investigations.

7788-20-7

Post Buying Request

7788-20-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

7788-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7788-20-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 8 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7788-20:
(6*7)+(5*7)+(4*8)+(3*8)+(2*2)+(1*0)=137
137 % 10 = 7
So 7788-20-7 is a valid CAS Registry Number.

7788-20-7Downstream Products

7788-20-7Relevant academic research and scientific papers

A new lupane-type triterpenoid fatty acid ester and other isolates from Ophiorrhiza shendurunii

Rajan, Renjith,Venkataraman, Ramaswamy,Baby, Sabulal

, p. 2197 - 2203 (2016/09/20)

A new pentacyclic triterpenoid fatty acid ester, lupan-20-ol-3(β)-yl hexadecanoate (1), together with lupan-20-ol-3(β)-yl acetate (2), olean-18-en-3(β)-yl hexadecanoate (3), dotriacontanoic acid (4), stigmasterol (5), rubiadin (6), nonadecanoic acid (7), palmitic acid (8) and camptothecin (9) were isolated from the hexane and chloroform extracts of Ophiorrhiza shendurunii from South India. Structures of the isolates were determined by1H,13C,13C DEPT,1H–1H COSY, HMBC, HSQC, NOESY NMR, FT-IR, DART-MS, ESI-MS, alkaline hydrolysis, derivatisation, GC–MS and HPTLC analyses. O. shendurunii hexane and chloroform extracts showed significant activities against Candida albicans and Fusarium oxysporum. Compounds 1 to 3 showed only moderate antiyeast/antifungal activities.

Lichens and Fungi. XVIII. Extractives from Pseudocyphellaria rubella

Corbett, R. Edward,Cong, Aimy N. T.,Holland, Patrick T.,Wilkins, Alistair L.

, p. 461 - 468 (2007/10/02)

Twenty lupane triterpenoids including five (20RS)-epimeric pairs have been isolated from the chloroform extractives of the lichen Pseudocyphellaria rubella.The utility of g.c.-m.s. procedures in the structural elucidation of the extractives, some of which were complex mixtures is discussed.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 7788-20-7