78804-17-8 Usage
Description
(-)-ZEYLENOL, also known as Sanchoenol, is an organic alcohol derived from the Sanjiaozi plant, which belongs to the genus Ziyupan of the Ansopaceae family. This plant is predominantly found in southern Guangdong and its islands, as well as in tropical and subtropical regions of South Asia and Southeast Asia. (-)-ZEYLENOL possesses notable anti-inflammatory and anti-tumor biological activities, making it a valuable compound for various applications.
Uses
Used in Pharmaceutical Research and Development:
(-)-ZEYLENOL is used as a pharmaceutical agent for its anti-inflammatory and anti-tumor properties. It is particularly valuable in scientific research experiments aimed at developing new treatments for inflammation and cancer.
Used in Drug Delivery Systems:
In the pharmaceutical industry, (-)-ZEYLENOL can be utilized as a component in drug delivery systems to enhance the efficacy and targeted delivery of anti-inflammatory and anti-tumor medications. This application can improve the bioavailability and therapeutic outcomes of such drugs.
Used in Nutraceuticals and Dietary Supplements:
Given its health-promoting properties, (-)-ZEYLENOL can be incorporated into nutraceuticals and dietary supplements to support anti-inflammatory and anti-tumor benefits for consumers seeking natural health solutions.
Used in Cosmetics and Personal Care:
Due to its anti-inflammatory properties, (-)-ZEYLENOL may also find use in the cosmetics and personal care industry, where it can be formulated into products designed to soothe and protect the skin, as well as promote overall skin health.
Check Digit Verification of cas no
The CAS Registry Mumber 78804-17-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,8,0 and 4 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 78804-17:
(7*7)+(6*8)+(5*8)+(4*0)+(3*4)+(2*1)+(1*7)=158
158 % 10 = 8
So 78804-17-8 is a valid CAS Registry Number.
InChI:InChI=1/C21H20O7/c22-17-12-11-16(20(25)28-15-9-5-2-6-10-15)18(23)21(17,26)13-27-19(24)14-7-3-1-4-8-14/h1-12,16-18,22-23,26H,13H2/t16-,17+,18+,21-/m1/s1
78804-17-8Relevant articles and documents
Stereoselective total synthesis of (?)-zeylenol, a key intermediate for the synthesis of (+)-pipoxide, (?)-uvarigranol G and (?)-tonkinenin A
Vinaykumar, Allam,Muniraju, Chinthala,Rao, Batchu Venkateswara
, p. 1075 - 1077 (2017)
Total synthesis of (?)-zeylenol, a key intermediate for the synthesis of (+)-pipoxide, (?)-uvarigranol G and (?)-tonkinenin A was achieved from commercially available starting material D-mannose. The key steps are mixed aldol condensation, Grignard reaction, ring closing metathesis and regioselective benzoylation.
The first enantiocontrolled synthesis of naturally occurring polyoxygenated cyclohexenylmethanol dibenzoates (-)-zeylenol, (-)-uvarigranol G, (-)-tonkinenin A and (+)-pipoxide
Hiroya, Kou,Ogasawara, Kunio
, p. 2197 - 2198 (2007/10/03)
The first enanticontrolled synthesis of five naturally occurring polyoxygenated cyclohexenylmethanol dibenzoates has been achieved to confirm three [(-)-zeylenol, (-)-uvarigranol G, (+)-pipoxide], revise one [(-)-tonkinenin A] and disprove one [(-)-epizey
STUDIES ON HIGHLY OXIDIZED CYCLOHEXANES.STRUCTURE AND ABSOLUTE CONFIGURATION ASSIGNMENTS.
Schulte, Gary R.,Ganem, Bruce
, p. 4299 - 4302 (2007/10/02)
The absolute configurations of pipoxide, ferrudiol and zeylenol, pictured below, are found to parallel those of crotepoxide and senepoxide, suggesting a unified biogenesis.
