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rac-3-Octadecanamido-2-Ethoxypropan-1-ol Phosphocholine is a colorless amorphous solid with strong inhibitory action against neoplastic cell growth in vitro and the ability to inhibit Protein Kinase C.

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  • 112989-02-3 Structure
  • Basic information

    1. Product Name: rac-3-Octadecanamido-2-Ethoxypropan-1-ol Phosphocholine
    2. Synonyms: 3-octadecanamido-2-ethoxypropylphosphocholine;7-Ethoxy-4-hydroxy-N,N,N-triMethyl-10-oxo-3,5-dioxa-9-aza-4-phosphaheptacosan-1-aMiniuM 4-oxide
    3. CAS NO:112989-02-3
    4. Molecular Formula: C28H59O6N2P?H2O
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: Mixed Fatty Acids;Fatty Acid Derivatives & Lipids;Glycerols;Inhibitors;Phosphorylcholine Derivatives;Protein Kinase Inhibitors and Activators
    8. Mol File: 112989-02-3.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: °Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: g/cm3
    6. Refractive Index: N/A
    7. Storage Temp.: -20°C Freezer
    8. Solubility: N/A
    9. CAS DataBase Reference: rac-3-Octadecanamido-2-Ethoxypropan-1-ol Phosphocholine(CAS DataBase Reference)
    10. NIST Chemistry Reference: rac-3-Octadecanamido-2-Ethoxypropan-1-ol Phosphocholine(112989-02-3)
    11. EPA Substance Registry System: rac-3-Octadecanamido-2-Ethoxypropan-1-ol Phosphocholine(112989-02-3)
  • 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: 112989-02-3(Hazardous Substances Data)

112989-02-3 Usage

Uses

Used in Pharmaceutical Industry:
rac-3-Octadecanamido-2-Ethoxypropan-1-ol Phosphocholine is used as a pharmaceutical agent for its strong inhibitory action against neoplastic cell growth in vitro, making it a potential candidate for cancer treatment.
Used in Biochemical Research:
rac-3-Octadecanamido-2-Ethoxypropan-1-ol Phosphocholine is used as a research tool for studying the role of Protein Kinase C in various cellular processes, as it has been shown to inhibit this enzyme.

Check Digit Verification of cas no

The CAS Registry Mumber 112989-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,9,8 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 112989-02:
(8*1)+(7*1)+(6*2)+(5*9)+(4*8)+(3*9)+(2*0)+(1*2)=133
133 % 10 = 3
So 112989-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C28H59N2O6P/c1-6-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-28(31)29-25-27(34-7-2)26-36-37(32,33)35-24-23-30(3,4)5/h27H,6-26H2,1-5H3,(H-,29,31,32,33)

112989-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name rac-3-Octadecanamido-2-ethoxypropan-1-ol Phosphocholine

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:112989-02-3 SDS

112989-02-3Downstream Products

112989-02-3Relevant articles and documents

Structure-activity relationship for enhancement of paracellular permeability across Caco-2 cell monolayers by 3-alkylamido-2-alkoxypropylphosphocholines

Ouyang, Hui,Morris-Natschke, Susan L.,Ishaq, Khalid S.,Ward, Peter,Liu, Dongzhou,Leonard, Sarah,Thakker, Dhiren R.

, p. 2857 - 2866 (2007/10/03)

Paracellular permeability enhancers have been used to improve the oral bioavailability of hydrophilic drugs; however, the mechanism of action of many enhancers is poorly understood. In this study, highly potent enhancers of paracellular permeability were

Structure-activity relationships for enhancement of paracellular permeability by 2-alkoxy-3-alkylamidopropylphosphocholines across Caco-2 cell monolayers

Liu, Dong-Zhou,Morris-Natschke, Susan L.,Kucera, Louis S.,Ishaq, Khalid S.,Thakker, Dhiren R.

, p. 1169 - 1174 (2007/10/03)

The oral route is the preferred route of delivery for a large number of drug molecules. However, the intestinal epithelium presents a formidable barrier for delivery of drugs into systemic circulation. Phospholipids are among compounds that enhance the ab

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