21887-01-4 Usage
Uses
Used in Pharmaceutical Industry:
Horminone is used as a therapeutic agent for its potential medicinal properties. The compound's unique structure and functional groups allow it to interact with biological targets, such as receptors or enzymes, which can lead to the development of new drugs for various diseases and conditions.
Used in Chemical Research:
Horminone serves as a valuable compound in chemical research, particularly in the study of diterpenoids and their derivatives. Its unique structure and properties make it an interesting subject for exploring new synthetic pathways, understanding its biological activities, and potentially discovering new applications in various fields.
Used in Drug Delivery Systems:
Similar to gallotannin, horminone can also be incorporated into drug delivery systems to enhance its bioavailability and therapeutic outcomes. By employing various carriers, such as organic and metallic nanoparticles, horminone can be effectively delivered to target cells or tissues, improving its overall efficacy and reducing potential side effects.
Check Digit Verification of cas no
The CAS Registry Mumber 21887-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,8 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21887-01:
(7*2)+(6*1)+(5*8)+(4*8)+(3*7)+(2*0)+(1*1)=114
114 % 10 = 4
So 21887-01-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H28O4/c1-10(2)13-16(22)14-11(21)9-12-19(3,4)7-6-8-20(12,5)15(14)18(24)17(13)23/h10-12,21,23H,6-9H2,1-5H3/t11-,12+,20+/m1/s1
21887-01-4Relevant articles and documents
A trihomoabietane diterpenoid from Plectranthus grandidentatus and an unusual addition of acetone to the ortho-quinone system of cryptotanshinone
Gaspar-Marques, Cristina,Simoes, M. Fatima,Rodriguez, Benjamin
, p. 1408 - 1411 (2008/09/18)
A new 9α-(2-oxopropyl)abietane derivative (1) has been isolated from an acetone extract of Plectranthus grandidentatus. Extraction of the plant material and analytical processes carried out in the absence of acetone also revealed the presence of 1 in the plant, thus suggesting that it is a natural product rather than an artifact. Attempts at obtaining Michael adducts between acetone and para-quinone abietane diterpenoids were unsuccessful, whereas treatment of the ortho-quinone cryptotanshinone (3) with acetone under basic conditions yielded compound 2. The structures of 1 and 2 were established by ID and 2D NMR spectroscopic studies.