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Aristolactam BIII is a chemical compound belonging to the aristolactam alkaloids group, which are natural products found in plants such as Aristolochia and Asarum. It has been identified for its potential toxic effects, particularly in relation to kidney damage and carcinogenicity, and is associated with aristolochic acid nephropathy (AAN), a condition characterized by chronic kidney disease and an increased risk of developing urothelial malignancies.

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  • 53948-10-0 Structure
  • Basic information

    1. Product Name: Aristolactam BIII
    2. Synonyms: Aristolactam BIII
    3. CAS NO:53948-10-0
    4. Molecular Formula: C18H15NO4
    5. Molecular Weight: 309.316
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53948-10-0.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: Aristolactam BIII(CAS DataBase Reference)
    10. NIST Chemistry Reference: Aristolactam BIII(53948-10-0)
    11. EPA Substance Registry System: Aristolactam BIII(53948-10-0)
  • 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: 53948-10-0(Hazardous Substances Data)

53948-10-0 Usage

Uses

Given the potential toxic effects of Aristolactam BIII, its uses are primarily focused on research and regulatory purposes to ensure the safety of herbal products and traditional medicines. However, it is important to note that due to its harmful effects, exposure to Aristolactam BIII should be limited.
Used in Pharmaceutical Research:
Aristolactam BIII is used as a research compound for studying its toxicological properties and potential role in renal fibrosis and urinary tract cancers. This helps in understanding the mechanisms of aristolochic acid nephropathy (AAN) and developing strategies to prevent or mitigate its harmful effects.
Used in Regulatory Compliance:
Aristolactam BIII is used as a marker for monitoring the presence of aristolactam alkaloids in herbal products and traditional medicines. Regulatory agencies may use this information to set safety standards and guidelines for the consumption of such products, ensuring that they do not contain harmful levels of aristolactam BIII and other aristolactam alkaloids.

Check Digit Verification of cas no

The CAS Registry Mumber 53948-10-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,4 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53948-10:
(7*5)+(6*3)+(5*9)+(4*4)+(3*8)+(2*1)+(1*0)=140
140 % 10 = 0
So 53948-10-0 is a valid CAS Registry Number.

53948-10-0SDS

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 1,2,9-Trimethoxydibenzo[cd,f]indol-4(5H)-one

1.2 Other means of identification

Product number -
Other names 3,4,6-trimethoxyaristolactame

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:53948-10-0 SDS

53948-10-0Downstream Products

53948-10-0Relevant articles and documents

Synthesis of aristolactam analogues and evaluation of their antitumor activity

Choi, Young Lok,Kim, Joa Kyum,Choi, Sang-Un,Min, Yong-Ki,Bae, Myung-Ae,Kim, Bum Tae,Heo, Jung-Nyoung

experimental part, p. 3036 - 3040 (2010/02/28)

A series of natural aristolactams and their analogues have been prepared and evaluated for antitumor activity against human cancer cells, including multi-drug resistant cell lines. Naturally occurring aristolactams, such as aristolactam BII (cepharanone B

PHENANTHRENE LACTAM DERIVATIVES HAVING ANTICANCER ACTIVITY AND METHOD FOR THE PREPARATION THEREOF

-

Page/Page column 19, (2009/05/28)

The present invention relates to a phenanthrene lactam derivative having anticanter activity, a method for the preparation thereof, and a pharmaceutical composition comprising same.

Total synthesis of aristolactams via a one-pot Suzuki-Miyaura coupling/aldol condensation cascade reaction

Kim, Joa Kyum,Kim, Young Ha,Nam, Ho Tae,Kim, Bum Tae,Heo, Jung-Nyoung

supporting information; experimental part, p. 3543 - 3546 (2009/05/07)

(Chemical Equation Presented) A direct one-pot synthesis of phenanthrene lactams, which employs a Suzuki -Miyaura coupling/aldol condensation cascade reaction of isoindolin-1-one with 2-formylphenylboronic acid, has been developed. The approach is used to

The Intramolecular Aryne Cycloaddition Approach to Aporphinoids. A New Total Synthesis of Aristolactams and Phenanthrene Alkaloids

Estevez, Juan C.,Estevez, Ramon J.,Castedo, Luis

, p. 10801 - 10810 (2007/10/02)

A new procedure for the total synthesis of aristolactams and phenanthrene alkaloids, based on the intramolecular Diels-Alder reaction between styrenes and arynes, is described.

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