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1'-O-acetylpaxilline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2H-Pyrano[2'',3'':5',6']benz[1',2':6,7]indeno[1,2-b]indol-3(4bH)-one,2-[1-(acetyloxy)-1-methylethyl]-5,6,6a,7,12,12b,12c,13,14,14a-decahydro-4b-hydroxy-12b,12c-dimethyl-,(2R,4bS,6aS,12bS,12cR,14aS)-

    Cas No: 121998-08-1

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  • 121998-08-1 Structure
  • Basic information

    1. Product Name: 1'-O-acetylpaxilline
    2. Synonyms: 1'-O-acetylpaxilline
    3. CAS NO:121998-08-1
    4. Molecular Formula: C29H35NO5
    5. Molecular Weight: 477.5919
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121998-08-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 653.8°Cat760mmHg
    3. Flash Point: 349.2°C
    4. Appearance: /
    5. Density: 1.29g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1'-O-acetylpaxilline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1'-O-acetylpaxilline(121998-08-1)
    11. EPA Substance Registry System: 1'-O-acetylpaxilline(121998-08-1)
  • 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: 121998-08-1(Hazardous Substances Data)

121998-08-1 Usage

Naturally occurring

1'-O-acetylpaxilline is found in certain types of fungi.

Indole alkaloid

It belongs to a class of chemical compounds that includes many alkaloids found in nature.

Derived from paxilline

It is a modified version of the parent compound paxilline.

Potent tremorgenic effects

It causes muscle tremors and other involuntary movements.

Selective blocker of voltage-gated potassium channels

It specifically targets and blocks these channels in neurons, leading to hyperexcitability and tremors.

Potential pharmacological effects

It has been studied for its ability to inhibit the growth of certain cancer cells and for its potential in treating conditions such as epilepsy and movement disorders.

Diverse biological activities

1'-O-acetylpaxilline has a range of biological activities and potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 121998-08-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,9,9 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 121998-08:
(8*1)+(7*2)+(6*1)+(5*9)+(4*9)+(3*8)+(2*0)+(1*8)=141
141 % 10 = 1
So 121998-08-1 is a valid CAS Registry Number.

121998-08-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1'-O-Acetylpaxilline

1.2 Other means of identification

Product number -
Other names 2H-1-Benzopyrano(5',6':6,7)indeno(1,2-b)indol-3(4bH)-one,2-(1-(acetyloxy)-1-methylethyl)-5,6,6a,7,12,12b,12c,13,14,14a-decahydro-4b-hydroxy-12b,12c-dimethyl-,(2R-(2alpha,4bbeta,6aalpha,12bbeta,12calpha,14abeta))

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:121998-08-1 SDS

121998-08-1Downstream Products

121998-08-1Relevant articles and documents

Isolation of a new tremorgenic indoloditerpene, 1'-O-acetylpaxilline, from Emericella striata and distribution of paxilline in Emericella spp.

Nozawa,Horie,Udagawa,Kawai,Yamazaki

, p. 1387 - 1389 (1989)

The distribution of a tremorgenic mycotoxin, paxilline (1), was investigated in 19 species belonging to the genus Emericella. It was found that Emericella desertorum, E. foveolata, and E. striata produced paxilline (1). A new type of indoloditerpene, emindole DA (4), was also found in E. quadrilineata. A new tremorgenic indoloditerpene, 1'-O-acetylpaxilline (3), was isolated from the mycelium of E. striata. Its structure was established on the basis of spectroscopic investigations.

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