42228-92-2 Usage
Chemical Properties
Off-White Solid
Originator
Acivicin ,ZYF Pharm Chemical
Uses
Different sources of media describe the Uses of 42228-92-2 differently. You can refer to the following data:
1. Inhibits glutamine amidotransferases in purine and pyrimidine synthetic pathways. Tumor growth inhibitor
2. Azaserine and Acivicin are classical and irreversible inhibitors of γ-Glutamyltranspeptidase
Definition
ChEBI: An L-alpha-amino acid that is L-alanine in which the methyl group is replaced by a (5S)-3-chloro-4,5-dihydro-1,2-oxazol-5-yl group. A glutamine analogue antimetabolite, it interferes with
lutamate metabolism and several glutamate-dependent synthetic enzymes. It is obtained as a fermentation product of Streptomyces sviceus bacteria.
Manufacturing Process
Starting from commercial, cis-2-buten-1,4-diol, the monotrichloroacetimidate
was obtained as a colorless liquid (60%, b.p. 88°-102°C/0.2 mm Hg) by
treatment with trichloroacetonitrile (1 equivalent) in tetrahydrofuran at -23°C
in the presence of catalytic amount of sodium. Monotrichloroacetimidate upon
refluxing in tert-butyl benzene for about 1 hour underwent, smoothly,rearrangement to afford the vinylglycine synton (84%, MP: 30°C). The
treatment of the last compound with bromonitrile oxide (3 equiv.) generated
in situ from dibromoformaldoxime in ethyl acetate containing excess of KHCO3
and trace amounts of water afforded 3:2 mixture of cycloadducts threo- and
erythro-N-[1-(3-bromo-4,5-dihydroisoxazol-5-yl)-2-hydroxyethyl]-2,2,2-
trichloroacetamide. The undesired threo- isomer (MP: 164°-165°C) was
quantitatively removed from the mixture by fractional crystallization from
chloroform. The erythro-isomer (oil) was refluxed with methanolic-HCl for 1
hour to give the chloro-alchohol (50%, syrup), which upon Jones oxidation
(with H2Cr2O7/acetone) followed by deprotection of trichloroacetyl group
(Ba(OH)2/H2O, H3+O) afforded racemic acivicin (66 %). The synthetic, racemic
antibiotic was spectrally (UV, 1H NMR) indistinguishable from
Therapeutic Function
Antineoplastic
Enzyme inhibitor
This cytotoxic isoxazole and copper chelator (FW = 178.57 g/mol; CAS 42228-92-2; Source: Streptomyces sviceus), also known as L-(aS,5S)-aamino-3-chloro-4,5-dihydro-5-isoxazoleacetic acid, AT-125, and NSC165301, strongly inhibitsγ-glutamyl transpeptidase. Its clinical application in cancer treatment failed as a consequence of unacceptable toxicity, and the cause(s) of the desired and undesired biological effects have never been elucidated and only limited information about acivicin-specific targets is available. Target deconvolution by quantitative mass spectrometry (MS) has now revealed acivicin’s preference for the specific aldehyde dehydrogenase known as ALDH4A1 by binding to the catalytic site. Moreover, siRNA-mediated downregulation of ALDH4A1 results in a severe inhibition of cell growth, a finding that may explain acivicin’s cytotoxicity. Targets: Acivicin is thought to be a glutamine analogue, an assumption that is amply supported by its ability to inhibit the following enzymes that possess essential amidohydrolase activities that generate nascent ammonia: asparagine synthetase; carbamoyl-phosphate synthetase; anthranilate synthase; glutamate synthase; CTP symthetase; amidophospho-ribosyltransferase; glutamin(asparagin)ase, or glutaminase-asparaginase; GMP synthase, glutamine-dependent; phosphoribosyl-formylglycinamidine synthetase (formylglycinamidine ribonucleotide synthetase; thiol oxidase; γ-glutamyl hydrolase; imidazole-glycerol phosphate synthetase.
Check Digit Verification of cas no
The CAS Registry Mumber 42228-92-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,2 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 42228-92:
(7*4)+(6*2)+(5*2)+(4*2)+(3*8)+(2*9)+(1*2)=102
102 % 10 = 2
So 42228-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C5H7ClN2O3/c6-3-1-2(11-8-3)4(7)5(9)10/h2,4H,1,7H2,(H,9,10)/t2-,4-/m0/s1
