Top Suppliers:I want be here

No recommended suppliers. I want be here

Related CAS#:
64118-43-0 60658-40-4
45135-30-6 5455-17-4
5455-16-3 93942-28-0
91258-67-2 93966-48-4
94086-75-6 93942-29-1

64118-43-0

64118-43-0 structure
64118-43-0 structure
  • Name: Undecanoic acid-d2
  • Chemical Name: 2,2-dideuteroundecanoic acid
  • CAS Number: 64118-43-0
  • Molecular Formula: C11H20D2O2
  • Molecular Weight: 188.30
  • Catalog: Signaling Pathways Anti-infection Fungal
  • Create Date: 2018-02-12 08:00:00
  • Modify Date: 2024-01-02 19:04:11
  • Undecanoic acid-d2 is the deuterium labeled Undecanoic acid. Undecanoic acid (Undecanoate) is a monocarboxylic acid with antimycotic property, which inhibits the production of exocellular keratinase, lipase and the biosynthesis of several phospholipids in T. rubrum[1].
Name 2,2-dideuteroundecanoic acid
Synonyms 5-AMinolevulinic-d2 Acid HCl
5-Aminolevulinic-2,2-D2 AcidHCI
5-Aminolevulinic-2,2-D2 AcidCI
2,2-dideutero-N-hendecanoic acid
2,2-dideutero-5-aminolevulinic acid hydrochloride
Description Undecanoic acid-d2 is the deuterium labeled Undecanoic acid. Undecanoic acid (Undecanoate) is a monocarboxylic acid with antimycotic property, which inhibits the production of exocellular keratinase, lipase and the biosynthesis of several phospholipids in T. rubrum[1].
Related Catalog
In Vitro Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].
References

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.

[2]. Hornung B, et al. Medium chain length fatty acids stimulate triacylglycerol synthesis in tissue culture cells. Biochem Pharmacol. 1992 Jan 22;43(2):175-81.

[3]. Das SK, et al. Effect of undecanoic acid on phospholipid metabolism in Trichophyton rubrum. Sabouraudia. 1982 Dec;20(4):267-72.

[4]. Das SK, et al. Effect of undecanoic acid on the production of exocellular lipolytic and keratinolytic enzymes by undecanoic acid-sensitive and -resistant strains of Trichophyton rubrum. Sabouraudia. 1982 Sep;20(3):179-84.

[5]. Coppa M, et al. Effect of a hay-based diet or different upland grazing systems on milk volatile compounds. J Agric Food Chem. 2011 May 11;59(9):4947-54.
Molecular Formula C11H20D2O2
Molecular Weight 188.30
Exact Mass 188.17500
PSA 37.30000
LogP 3.60180
334026-57-2 structure

334026-57-2

~%

64118-43-0 structure

64118-43-0
Literature: Buist, Peter H.; Behrouzian, Behnaz Journal of the American Chemical Society, 1996 , vol. 118, # 26 p. 6295 - 6296
334-48-5 structure

334-48-5

~%

64118-43-0 structure

64118-43-0
Literature: Buist, Peter H.; Behrouzian, Behnaz Journal of the American Chemical Society, 1996 , vol. 118, # 26 p. 6295 - 6296
42006-99-5 structure

42006-99-5

~%

64118-43-0 structure

64118-43-0
Literature: Buist, Peter H.; Behrouzian, Behnaz Journal of the American Chemical Society, 1996 , vol. 118, # 26 p. 6295 - 6296
177654-03-4 structure

177654-03-4

~%

64118-43-0 structure

64118-43-0
Literature: Buist, Peter H.; Behrouzian, Behnaz Journal of the American Chemical Society, 1996 , vol. 118, # 26 p. 6295 - 6296
Precursor  3

DownStream  0


Chemsrc provides CAS#:64118-43-0 MSDS, density, melting point, boiling point, structure, formula, molecular weight, synthetic route, etc.
title: CAS No. 64118-43-0 | Chemsrc address: https://www.chemsrc.com/en/baike/88740.html

Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer

Copyright © 2024 ChemSrc All Rights Reserved