D-Pantethine
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D-Pantethine
structure -
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CAS No:
16816-67-4
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Formula:
C22H42N4O8S2
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Chemical Name:
D-Pantethine
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Synonyms:
bis(pantothenamidoethyl)disulfide;butyramide,n,n’-(dithiobis(ethyleneiminocarbonylethylene))bis(2,4-dihydroxy-3,;d-(+)-3-dimethyl;d-bis(n-pantothenyl-beta-aminoethyl)disulfide;d-pantethineanhydrous;lbfdisulfide;PANTETHIN;Butanamide, N,N-dithiobis2,1-ethanediylimino(3-oxo-3,1-propanediyl)bis2,4-dihydroxy-3,3-dimethyl-, (2R,2R)-
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CAS No:
Description
Colorless to pale yellow, clear, viscous liquidChEBI: An organic disulfide that consists of two molecules of pantothenic acid linked by amide bonds to a cysteamine disulfide bridging group.
Bis(N-pantothenylamidoethyl) disulfide is an organonitrogen compound and an organooxygen compound. It derives from a beta-amino acid.
D-Pantethine is a compound in which two molecules of D-pantetheine bind through an S-S linkage. D-Pantethine is available from commercial sources as well as from D-pantothenic acid. It is known that the sulfhydryl group is the metabolically active part of the molecule. Coenzyme A is an essential cofactor in over 70 biological pathways, such as fatty acid oxidation, carbohydrate metabolism, and amino acid catabolism. Studies conducted in vitro suggest that D-Pantethine inhibits the activity of aldehyde dehydrogenase; however, related metabolites of the compound, such as Taurine (sc-202354), D-pantetheine, Coenzyme A, and D-pantothenate activate this enzyme.
Colorless to pale yellow, clear, viscous liquid
Moderately toxic by intravenous route. An experimental teratogen. Experimental reproductive effects. When heated to decomposition it emits toxic fumes of SOx and NOx.
Characteristics
248
-2.2
syrup
1.1949 (rough estimate)
987.2±65.0 °C(Predicted)
550.8ºC
1.6000 (estimate)
2-8°C
0mmHg at 25°C
LD50 oral in rat: > 10gm/kg
D27 +13.5° (c = 3.75 in water)
12.71±0.20(Predicted)
2-8°C
Computed Properties
Molecular Weight:554.7
XLogP3:-2.2
Hydrogen Bond Donor Count:8
Hydrogen Bond Acceptor Count:10
Rotatable Bond Count:19
Exact Mass:554.24440666
Monoisotopic Mass:554.24440666
Topological Polar Surface Area:248
Heavy Atom Count:36
Complexity:652
Undefined Atom Stereocenter Count:2
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
It improves fat metabolism, reduces triglycerides, accelerates the β-oxidation process of fatty acids in the liver and arterial walls, and inhibits fat peroxidation products. It also increases the activity of fat metabolism enzymes and cholesterol esterase, and increases the content of high-density lipid cholesterol in serum.
Registered Holders
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Yifan Pharmaceutical Co., Ltd.
Active
China
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Hefei Cosource Heyuan Pharmaceutical Co., Ltd.
Active
China
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SIGMA F AND D DIV LTD
Inactive
United States
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