481-70-9 Usage
Description
Endocrocin, also known as emodin, is a trihydroxyanthraquinone derived from various plant sources. It is characterized by its chemical structure, which includes a carboxy group at position 2, a methyl group at position 3, and hydroxy groups at positions 1, 6, and 8. Endocrocin has been recognized for its potential pharmaceutical applications due to its bioactive properties.
Uses
Used in Pharmaceutical Industry:
Endocrocin is used as a pharmaceutical compound for its various bioactive properties. It has been found to possess anti-inflammatory, antioxidant, and anticancer activities. endocrocin is particularly effective against certain types of cancer cells, making it a promising candidate for cancer treatment.
Used in Traditional Medicine:
Endocrocin has been utilized in traditional medicine for centuries, particularly in the treatment of gastrointestinal disorders, inflammation, and certain skin conditions. Its natural occurrence in various plants has made it an important component in herbal remedies and traditional formulations.
Used in Drug Delivery Systems:
Similar to gallotannin, endocrocin can also be incorporated into drug delivery systems to enhance its bioavailability and therapeutic outcomes. By using carriers such as organic and metallic nanoparticles, the limitations of endocrocin can be overcome, leading to improved delivery and efficacy against target conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 481-70-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 1 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 481-70:
(5*4)+(4*8)+(3*1)+(2*7)+(1*0)=69
69 % 10 = 9
So 481-70-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H10O7/c1-5-2-7-12(14(20)10(5)16(22)23)15(21)11-8(13(7)19)3-6(17)4-9(11)18/h2-4,17-18,20H,1H3,(H,22,23)
481-70-9Relevant articles and documents
Steglich,Reininger
, p. 178 (1970)
Physically Discrete β-Lactamase-Type Thioesterase Catalyzes Product Release in Atrochrysone Synthesis by Iterative Type I Polyketide Synthase
Awakawa, Takayoshi,Yokota, Kosuke,Funa, Nobutaka,Doi, Fuminao,Mori, Naoki,Watanabe, Hidenori,Horinouchi, Sueharu
experimental part, p. 613 - 623 (2010/04/22)
ATEG_08451 in Aspergillus terreus, here named atrochrysone carboxylic acid synthase (ACAS), is a nonreducing, iterative type I polyketide synthase that contains no thioesterase domain. In vitro, reactions of ACAS with malonyl-CoA yielded a polyketide inte
Studies on Nepalese crude drugs. XXV. Phenolic constituents of the leaves of Didymocarpus leucocalyx C. B. Clarke (Gesneriaceae)
Segawa, Akiko,Miyaichi, Yukinori,Tomimori, Tsuyoshi,Kiuchi, Fumiyuki,Ohta, Tomihisa
, p. 1404 - 1411 (2007/10/03)
Seven new phenolic compounds (814) including three ones having unique structure named didymocalyxins A (12), B (13) and C (14) have been isolated from the leaves of Didymocarpus leucocalyx, along with five known flavonoids (5-hydroxy-6,7-dimethoxyflavanon