Cholesterol
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Cholesterol
structure -
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CAS No:
57-88-5
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Formula:
C27H46O
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Chemical Name:
Cholesterol
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Synonyms:
Cholest-5-en-3-ol (3β)-;Cholesterol;(3β)-Cholest-5-en-3-ol;Cholest-5-en-3β-ol;Cholesterin;5:6-Cholesten-3β-ol;Dythol;3β-Hydroxycholest-5-ene;Provitamin D;Cholesteryl alcohol;(-)-Cholesterol;Δ5-Cholesten-3β-ol;Lidinit;Lidinite;NSC 8798;SyntheChol;Marine Cholesterol;80356-14-5;80356-33-8;209124-38-9;218965-24-3;262418-13-3;378185-03-6;676322-57-9;732297-95-9;793670-51-6;849593-11-9;856708-55-9;2016865-06-6;2363129-31-9
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CAS No:
Description
Cholesterol is the major sterol in mammals, and its importance in fundamental cellular processes is becoming more appreciated. IC50 value:Target:In vitro: GT1-7 hypothalamic cells subjected to cholesterol depletion in vitro produced 20-31% reductions in cellular cholesterol content, similar to the decrease in cholesterol synthesis observed in diabetes [1].In vivo:
Vat Yellow 1 is sort of vat dye. Molecular structure of Vat Yellow 1 is anthraquinone.
Characteristics
20.23000
7.38870
Solid
1.067 g/cm3 @ Temp: 20 °C
148.5 °C
360 °C
250ºC
1.525
H2O: negligible soluble
2-8ºC
Specific rotation: -34 to 38 deg @ 25 °C
Almost odorless
Safety Information
UN 1170 3/PG 3
1
R10
S22-S24/25
FZ8400000
Xn
Stable under normal shipping and handling conditions.
P201-P261-P304 + P340 + P312-P305 + P351 + P338-P308 + P313-P403 + P233
H302-H315-H319-H331-H336-H351-H361d-H372
UN 1170 3/PG 3
Cholesterol Use and Manufacturing
1. Analeptic, antibacterial
2. Cholesterol is a major component of all biological membranes; ~25% of total brain lipid is Cholesterol. Cholesterol is the principal sterol of the higher animals. Cholesterol was found in all body tissues, especial in the brain, spinal cord, and in animal fats or oils. Cholesterol is the main constituent of gallstones.
3. Cholesterol be used as pharmaceutical intermediates and be used as synthetic materials of liquid crystal polymers.
Cholest-5-en-3-ol (3.beta.)-: ACTIVE
Computed Properties
Molecular Weight:386.7
XLogP3:8.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:386.354866087
Monoisotopic Mass:386.354866087
Topological Polar Surface Area:20.2
Heavy Atom Count:28
Complexity:591
Undefined Atom Stereocenter Count:8
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Synthesis Route
97838-91-0
212069-44-8
257939-67-6
88674-22-0
257939-67-6
Drug Function and Efficacy
This product is a compound external ointment. Its main ingredient, ginsenoside, has the characteristics of non-ionic surface activity. It can directly enter the interior of the hair fiber and connect with the hydrophilic groups in the hair keratin through the hydroxyl groups in the ginsenoside molecules, thereby improving the tensile strength and elongation of the hair. Pepper tincture improves scalp blood circulation, and together with anti-seborrheic drugs such as diethylstilbestrol and salicylic acid, it reduces sebum secretion, increases hair follicle nutrition, improves excessive keratinization of the hair follicle mouth, and stimulates the hair growth function of the affected scalp.
Registered Holders
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CARBOGEN AMCIS BV
Active
United States
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Jiangsu Southeast NanoMaterials Co., Ltd.
Active
China
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Hunan Er-Kang Pharmaceutical Co., Ltd.
Active
China
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