Description Source Function Biosynthesis pathway
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LANOSTEROL

Description Source Function Biosynthesis pathway
Product Name
LANOSTEROL
CAS No.
79-63-0
Chemical Name
LANOSTEROL
Synonyms
Lanosterin;Lanster;DUSOGEL;LANOSTEROL;lanostcrol;botalanbase;CRYPTOSTEROL;Criptosterol;Kriptosterol;Kryp-tosterol
CBNumber
CB6266873
Molecular Formula
C30H50O
Formula Weight
426.73
MOL File
79-63-0.mol
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LANOSTEROL Property

Melting point:
137 °C
alpha 
D20 +62.0° (chloroform)
Boiling point:
482.1°C (rough estimate)
Density 
0.9600 (rough estimate)
refractive index 
1.4910 (estimate)
storage temp. 
-20°C
solubility 
Chloroform (Slightly), Ethyl Acetate (Slightly)
pka
15.16±0.70(Predicted)
form 
powder
color 
white
Odor
at 100.00?%. bland
Merck 
5360
InChIKey
CAHGCLMLTWQZNJ-BQNIITSRSA-N
LogP
10.521 (est)
CAS DataBase Reference
79-63-0(CAS DataBase Reference)
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Safety

WGK Germany 
1
RTECS 
OE3360000
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
L5768
Product name
Lanosterol
Purity
≥93%, powder
Packaging
1mg
Price
$126
Updated
2024/03/01
Sigma-Aldrich
Product number
L5768
Product name
Lanosterol
Purity
≥93%, powder
Packaging
5mg
Price
$445
Updated
2024/03/01
Cayman Chemical
Product number
19521
Product name
Lanosterol
Purity
≥95%
Packaging
1mg
Price
$77
Updated
2024/03/01
Cayman Chemical
Product number
19521
Product name
Lanosterol
Purity
≥95%
Packaging
5mg
Price
$340
Updated
2024/03/01
Cayman Chemical
Product number
19521
Product name
Lanosterol
Purity
≥95%
Packaging
10mg
Price
$602
Updated
2024/03/01
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LANOSTEROL Chemical Properties,Usage,Production

Description

Lanosterol occurs naturally in the eyes of mammals and has been shown to dissolve cataracts by revitalizing damaged cataract-causing crystallin proteins. Lanosterol’s amphipathic nature is believed to play a large role in its ability to prevent and reverse cataract formation.

Source

Lanosterol is the first sterol in lipid biosynthetic pathway, which is initially converted by acetyl-CoA. The complex process of lanosterol synthesis involves several enzymes, including 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase, squalene epoxidase, and lanosterol synthase (LSS). LSS is a microsomal enzyme that functions as a downstream element in the lanosterol biosynthetic pathway, catalyzing the cyclization of the linear 2,3-monoepoxysqualene to lanosterol.

Function

A cytochrome P450 monooxygenase involved in sterol biosynthesis. Catalyzes 14-alpha demethylation of lanosterol and 24,25-dihydrolanosterol likely through sequential oxidative conversion of 14-alpha methyl group to hydroxymethyl, then to carboxylaldehyde, followed by the formation of the delta 14,15 double bond in the sterol core and concomitant release of formic acid (PubMed:20149798, PubMed:8619637). Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase.

Biosynthesis pathway

The lanosterol pathway refers to a segment of the cholesterol biosynthesis pathway comprising twelve enzymes, namely acetyl-CoA acetyltransferase, hydroxymethylglutaryl-CoA synthase, hydroxymethylglutaryl-CoA reductase, mevalonate kinase, phosphomevalonate kinase, diphoshomevalonate decarboxylase, isopentenyl-diphosphate delta isomerase, geranylgeranyl diphosphate synthase, farnesyl diphosphate synthase, squalene synthase, squalene monooxygenase and lanosterol synthase. The lanosterol pathway describes the stages of cholesterol biosynthesis between the conversion of substrates acetyl CoA and acetoacetyl CoA to (S)-3-hydroxy-3-methylglutaryl-CoA, through to the formation of intermediate metabolite lanosterol, the precursor of cholesterol. Metabolites of the lanosterol pathway are either directed to the synthesis of cholesterol and other sterols, or to side branches of the pathway through which they are converted to isoprenoids and other non-sterols.

Description

Lanosterol is a naturally-occurring sterol and biosynthetic precursor of several animal, fungal, and protozoan steroids, including cholesterol and ergosterol. Defects in the processing of lanosterol contribute to a wide variety of disorders, including the formation of cataracts. Similarly, certain fungicides act by blocking lanosterol processing by fungi.

Uses

Lanosterol has been used:

  • as a standard in HPLC for the quantification in testis samples
  • in S-adenosyl-L-methionine:Δ24-sterol-C-methyltransferase (SMT) assay
  • to treat wild-type cells growing in rich medium to know its effects on Sre1 protein

Definition

ChEBI: A tetracyclic triterpenoid that is lanosta-8,24-diene substituted by a beta-hydroxy group at the 3beta position. It is the compound from which all steroids are derived.

General Description

Lanosterol, an amphipathic molecule, that is produced by?lanosterol?synthase (LSS). It is enriched in the lens.

Biochem/physiol Actions

Cholesterol precursor sterol.Lanosterol serves as an endogenous selective modulator of macrophage immunity.

Purification Methods

If very impure, then it should be acetylated, converted to the dibromide acetate [crystallised from EtOAc with slow cooling, m 168-170o, [] D +214o (CHCl3)], de-brominated with Zn dust to give the acetate (below) which is recrystallised from 3-4 parts of Me2CO/MeOH (4:1) and hydrolysed as for stigmasterol (below). Recrystallise it from anhydrous MeOH. Dry it in vacuo over P2O5 for 3hours at 90o. The purity is checked by proton magnetic resonance. The acetate crystallises from MeOH with m 131-133o and [ ] 25D +62o (c 1,CHCl3). [Block & Urech Biochemical Preparations 6 32 1958. van Tamelen et al. J Am Chem Soc 104 6479, 6480 1982, Beilstein 6 III 2880, 6 IV 4188.]

LANOSTEROL Preparation Products And Raw materials

Raw materials

Preparation Products

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LANOSTEROL Suppliers

TCI Europe
Tel
320-37350700
Fax
+32 (0)37350701
Email
sales@tcieurope.eu
Country
Europe
ProdList
23671
Advantage
75
ecochem international chemical broker
Tel
--
Fax
--
Email
export@ecochem.dk
Country
Europe
ProdList
6371
Advantage
66
kemikalieimport
Tel
--
Fax
--
Email
Sales@kemikalieimport.dk
Country
Europe
ProdList
6685
Advantage
47
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View Lastest Price from LANOSTEROL manufacturers

WUHAN FORTUNA CHEMICAL CO., LTD
Product
Lanosterol 79-63-0
Price
US $0.00-0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500kgs/month
Release date
2024-06-04
Hebei Zhuanglai Chemical Trading Co Ltd
Product
Lanosterol 79-63-0
Price
US $150.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
500kg
Release date
2024-12-10
Hebei Chuanghai Biotechnology Co,.LTD
Product
Lanosterol 79-63-0
Price
US $8.70/KG
Min. Order
10KG
Purity
99%
Supply Ability
10000kg
Release date
2024-08-21

79-63-0, LANOSTEROLRelated Search:


  • Lanosterol (Isocholesterol)
  • (3-beta)-lanosta-24-dien-3-ol
  • (3-beta)-lanosta-8,24-dien-3-ol
  • lanosta-8,24-dien-3-beta-ol
  • Lanosta-8,24-dien-3beta-ol
  • Lanosta-8,24-dien-3-ol
  • Lanosta-8,24-dien-3-ol, (3beta)-
  • Lanosta-8,24-dienol
  • lanostadien-3-beta-ol
  • Lanosterin
  • lanosterol50-60%
  • Lanster
  • 24-dien-3-ol,(3.beta.)-Lanosta-8
  • CRYPTOSTEROL
  • LANOSTEROL
  • ISOCHOLESTEROL
  • 3BETA-HYDROXY-8,24-LANOSTADIENE
  • 8,24-LANOSTADIEN-3BETA-OL
  • 8,24-LANOSTADIEN-3-OL
  • 8,24-LANOSTADIENE-3BETA-OL
  • 8,24,(5-ALPHA)-CHOLESTADIEN-4,4,14-ALPHA-TRIMETHYL-3-BETA-OL
  • 8,24,(5ALPHA)-CHOLESTADIEN-4,4,14ALPHA-TRIMETYHL-3BETA OL
  • (3S,5S,10S,13S,14S)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
  • Lanosta-8,24-dien-3-ol,(3b)-
  • Botalan base 138
  • botalanbase
  • Cholesta-8,24-dien-3-ol, 4,4,14-trimethyl-, (3beta,5alpha)-
  • lanosterol approx. 97%
  • LANOSTEROL ABOUT 55-65%
  • LANOSTEROL 95%
  • 3β-hydroxy-8,24-lanostadiene
  • 4,4,10,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
  • LANOSTEROL(RG)
  • DUSOGEL
  • LANOSTEROL ~60% PURE
  • 3β-Hydroxy-8,24-lanostadiene, 8,24-Lanostadien-3β-ol
  • 5α-Lanosta-8,24-dien-3β-ol
  • 5α-Lanosta-8,24-diene-3β-ol
  • Criptosterol
  • Kriptosterol
  • 8,24(5α)-Cholestadien-4,4,14α-triMethyl-3β-ol
  • Kryp-tosterol
  • LANOSTEROL (FROM NATURAL SOURCES)
  • LANOSTA-8,24-DIEN-3-OL;LANOSTEROL
  • lanostcrol
  • LANOSTEROL, >/=93%, POWDER
  • Lanosterol (Isocholesterol) - Lanosterol 60%
  • Lanosterol &gt
  • Lanosterol (Technical Grade)
  • Lanosta-8,24-dien-3-ol, (3β)-
  • LANOSTEROL USP/EP/BP
  • (3S,5R,10S,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol
  • (3β)-Lanosta-8,24-dien-3-ol
  • Lanosterol pure, ~60%
  • 3β-Hydroxy-8,24-lanostadiene
  • 8,24-Lanostadien-3β-ol
  • (3S,5R,10S,13R,14R,17R)-4,4,10,13,14-Pentamethyl-17-((R)-6-methylhept-5-en-2-yl)-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
  • Garlic oil 8008-99-9