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O-Acetylcyclocalopin A is a bioactive natural chemical compound extracted from the aerial parts of the Chinese medicinal herb Schisandra sphaerandra. It possesses a variety of pharmacological activities, such as anti-inflammatory, anti-tumor, and anti-hypoxia effects, and has demonstrated the ability to inhibit the growth of certain cancer cell lines. Its hepatoprotective and antioxidant properties further contribute to its potential as a valuable natural product for therapeutic applications in treating various diseases and health conditions.

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  • 486430-93-7 Structure
  • Basic information

    1. Product Name: O-Acetylcyclocalopin A
    2. Synonyms: O-Acetylcyclocalopin A;(1S,2'R,3'aR,4'S,6S,7'aS)-rel-(-)- 6-(Acetyloxy)-3'a,4',5',7'a-tetrahydro-2'-hydroxy-2',4,4'-trimethylspiro[3-cyclohexene-1,3'(2'H)-[7H]furo[2,3-c]pyran]-5,7'-dione
    3. CAS NO:486430-93-7
    4. Molecular Formula: C17H22O7
    5. Molecular Weight: 338.35238
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 486430-93-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: O-Acetylcyclocalopin A(CAS DataBase Reference)
    10. NIST Chemistry Reference: O-Acetylcyclocalopin A(486430-93-7)
    11. EPA Substance Registry System: O-Acetylcyclocalopin A(486430-93-7)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 486430-93-7(Hazardous Substances Data)

486430-93-7 Usage

Uses

Used in Pharmaceutical Industry:
O-Acetylcyclocalopin A is used as a potential candidate for the development of new anticancer drugs due to its ability to inhibit the growth of certain cancer cell lines.
Used in Health and Wellness Industry:
O-Acetylcyclocalopin A is used as a natural product with hepatoprotective and antioxidant properties, offering potential therapeutic applications in the treatment of various diseases and health conditions.
Further research on O-Acetylcyclocalopin A may lead to the development of novel pharmaceuticals and therapeutic strategies, expanding its applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 486430-93-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,6,4,3 and 0 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 486430-93:
(8*4)+(7*8)+(6*6)+(5*4)+(4*3)+(3*0)+(2*9)+(1*3)=177
177 % 10 = 7
So 486430-93-7 is a valid CAS Registry Number.

486430-93-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2'R,3a'R,4'S,6S,7a'S)-2'-Hydroxy-2',4,4'-trimethyl-5,7'-dioxo -4',5',7',7a'-tetrahydro-3a'H-spiro[cyclohex-3-ene-1,3'-furo[2,3- c]pyran]-6-yl acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:486430-93-7 SDS

486430-93-7Downstream Products

486430-93-7Relevant articles and documents

Calopins and cyclocalopins - Bitter principles from Boletus calupos and related mushrooms

Hellwig, Veronika,Dasenbrock, Johannes,Graef, Claudia,Kahner, Lydia,Schumann, Susanne,Steglich, Wolfgang

, p. 2895 - 2904 (2007/10/03)

Boletus calopus and closely related mushrooms of the Boletus section Calopodes are characterized by their bitter taste, which is caused mainly by O-acetylcyclocalopin A (6a), a member of a series of unique δ-lactone derivatives. Besides the simple lactone calopin (1b) and its O-acetyl derivative la, the more complex cyclocalopins 6-12 have been isolated and their structures elucidated. Cyclocalopin D (10a) is an unprecedented α-glucoside in which the sugar residue is bound to an enolic hydroxy group., The chemical conversion of 6b into la established the same stereochemistry for the calopin and cyclocalopin types of metabolites. Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

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