ChemicalBook > CAS DataBase List > 2-(PROPYL-2,2-D2)PENTANOIC-4,4-D2 ACID

2-(PROPYL-2,2-D2)PENTANOIC-4,4-D2 ACID

Product Name
2-(PROPYL-2,2-D2)PENTANOIC-4,4-D2 ACID
CAS No.
345909-03-7
Chemical Name
2-(PROPYL-2,2-D2)PENTANOIC-4,4-D2 ACID
Synonyms
Valproic-d4 Acid;Valproic acid (4,4,4',4'-D4);Valproic acid (4,4,4′,4′-D?, 98%);2-(Propyl-2,2-d2)pentanoic--d2 Acid;2-(PROPYL-2,2-D2)PENTANOIC-4,4-D2 ACID
CBNumber
CB1235726
Molecular Formula
C8H16O2
Formula Weight
144.21
MOL File
345909-03-7.mol
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
V947836
Product name
Valproic-d4Acid
Packaging
11mg
Price
$60
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
RDL0007289
Product name
PENTANOIC-4,4-D2-ACID,2-(PROPYL-2,2-D2)-
Purity
95.00%
Packaging
5MG
Price
$550
Updated
2021/12/16
Medical Isotopes, Inc.
Product number
D574
Product name
2-(Propyl-2,2-d2)pentanoic-4,4-d2Acid
Packaging
0.1g
Price
$1525
Updated
2021/12/16
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2-(PROPYL-2,2-D2)PENTANOIC-4,4-D2 ACID Chemical Properties,Usage,Production

Uses

Valproic acid-d4-1 is the deuterium labeled Valproic acid. Valproic acid (VPA; 2-Propylpentanoic Acid) is an HDAC inhibitor, with IC50 in the range of 0.5 and 2 mM, also inhibits HDAC1 (IC50, 400 μM), and induces proteasomal degradation of HDAC2. Valproic acid activates Notch1 signaling and inhibits proliferation in small cell lung cancer (SCLC) cells. Valproic acid sodium salt is used in the treatment of epilepsy, bipolar disorder and prevention of migraine headaches[1][2].

References

[1] Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216. DOI:10.1177/1060028018797110
[2] Valproic acid, et al. Histone deacetylase is a direct target of valproic acid, a potent anticonvulsant, mood stabilizer, and teratogen. J Biol Chem. 2001 Sep 28;276(39):36734-41. DOI:10.1074/jbc.M101287200
[3] Han BR, et al. Valproic acid inhibits the growth of HeLa cervical cancer cells via caspase-dependent apoptosis. Oncol Rep. 2013 Dec;30(6):2999-3005. DOI:10.3892/or.2013.2747
[4] Zhang ZH, et al. Valproic acid inhibits tumor angiogenesis in mice transplanted with Kasumi 1 leukemia cells. Mol Med Rep. 2013 Nov 28. DOI:10.3892/mmr.2013.1834
[5] Cohen OS, et al. Acute prenatal exposure to a moderate dose of valproic acid increases social behavior and alters gene expression in rats. Int J Dev Neurosci. 2013 Dec;31(8):740-50. DOI:10.1016/j.ijdevneu.2013.09.002
[6] Avery LB, et al. Valproic Acid Is a Novel Activator of AMP-Activated Protein Kinase and Decreases Liver Mass, Hepatic Fat Accumulation, and Serum Glucose in Obese Mice. Mol Pharmacol. 2014 Jan;85(1):1-10. DOI:10.1124/mol.113.089755
[7] Platta CS, et al. Valproic acid induces Notch1 signaling in small cell lung cancer cells. J Surg Res. 2008 Jul;148(1):31-7. DOI:10.1016/j.jss.2008.03.008

2-(PROPYL-2,2-D2)PENTANOIC-4,4-D2 ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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2-(PROPYL-2,2-D2)PENTANOIC-4,4-D2 ACID Suppliers

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345909-03-7, 2-(PROPYL-2,2-D2)PENTANOIC-4,4-D2 ACIDRelated Search:


  • 2-(Propyl-2,2-d2)pentanoic--d2 Acid
  • 2-(PROPYL-2,2-D2)PENTANOIC-4,4-D2 ACID
  • Valproic-d4 Acid
  • Valproic acid (4,4,4',4'-D4)
  • Valproic acid (4,4,4′,4′-D?, 98%)
  • 345909-03-7
  • CH3CD2CH22CHCOOH