CB 3717

CB 3717 Suppliers list
Company Name: SPIRO PHARMA  
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Email: eric_feng1954@126.com
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Company Name: TargetMol Chemicals Inc.  
Tel: 13564774135
Email: marketing@targetmol.com
Company Name: Hu Bei Jiutian Bio-medical Technology CO.,Ltd  
Tel: 027-88013699 17354350817
Email: Ryan@jiutian-bio.com

CB 3717 manufacturers

  • CB 3717
  • CB 3717 pictures
  • $3480.00
  • 2026-05-21
  • CAS:76849-19-9
  • Purity:
  • Supply Ability: 10g
CB 3717 Basic information
Product Name:CB 3717
Synonyms:CB 3717;10-Propargyl-5,8-dideazafolate;N-[4-[[(2-Amino-1,4-dihydro-4-oxoquinazolin-6-yl)methyl]-2-propynylamino]benzoyl]-L-glutamic acid;N-[p-[Propargyl(2-amino-4-hydroxyquinazolin-6-ylmethyl)amino]benzoyl]-L-glutamic acid;LTKHPMDRMUCUEB-IBGZPJMESA-N;L-Glutamic acid, N-[4-[[(2-amino-3,4-dihydro-4-oxo-6-quinazolinyl)methyl]-2-propyn-1-ylamino]benzoyl]-;8-dideazafolic acid;N(sup 10)-Propargyl-5
CAS:76849-19-9
MF:C24H23N5O6
MW:477.47
EINECS:
Product Categories:
Mol File:76849-19-9.mol
CB 3717 Structure
CB 3717 Chemical Properties
Safety Information
MSDS Information
CB 3717 Usage And Synthesis
DescriptionCB 3717, a potent inhibitor of thymidylate synthase, is toxic for cell lines with altered dihydrofolate reductase; and homofolate, a de novo purine inhibitor requiring dihydrofolate reductase for activation, is effective in reductase-amplified lines.
UsesCB 3717 is a potent inhibitor of human thymidylate synthetase, competitively binding with 5,10-methylenetetrahydrofolate (Ki = 4.9 X 10(-9) M). It also competitively inhibits human dihydrofolate reductase with dihydrofolate (Ki = 2.3 X 10(-8) M). In WI-L2 human lymphoblastoid cells, CB 3717 treatment led to a significant decrease in cellular dTTP levels and a notable increase in dUMP levels, indicating a disruption in nucleotide metabolism. The growth-inhibitory effect of CB 3717 was reversed by thymidine supplementation, demonstrating that thymidylate synthetase became rate-limiting in the presence of this compound. Delayed thymidine supplementation beyond 8 hours resulted in severe cytotoxicity, underscoring the critical timing of nucleotide rescue strategies in CB 3717-treated cells[1].
DefinitionChEBI: CB3717 is a N-acyl-L-glutamic acid.
HazardA poison.
References[1] Biochemical effects of a quinazoline inhibitor of thymidylate synthetase, N-(4-(N-(( 2-amino-4-hydroxy-6-quinazolinyl)methyl)prop-2-ynylamino) benzoyl)-L-glutamic acid (CB3717), on human lymphoblastoid cells DOI:10.1016/0006-2952(83)90150-8
CB 3717 Preparation Products And Raw materials
Tag:CB 3717(76849-19-9) Related Product Information
ICI 198583 5,8-Dideazapteroylornithine CB 3717 10-formyl-5,8-dideazafolate CB 3705 Disuccinimidyl glutarate