Description Source Function Biosynthesis pathway
ChemicalBook > CAS DataBase List > LANOSTEROL

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
More
Less

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)
More
Less

Safety

WGK Germany 
1
RTECS 
OE3360000
More
Less

Hazard and Precautionary Statements (GHS)

More
Less

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
More
Less

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

More
Less

LANOSTEROL Suppliers

Jay Chemicals
Tel
13732234254
Email
yogesh.dama@jaychemicals.co.in
Country
China
ProdList
41
Advantage
58
Shandong JunRui Pharmaceutical Co., Ltd.
Tel
0539-5636807 15318528770
Fax
0539-5636807
Email
ffeng813@qq.com
Country
China
ProdList
247
Advantage
58
Sichuan BioCrick Biotech Co., Ltd
Tel
28-85433893
Email
info@biocrick.com
Country
CHINA
ProdList
4988
Advantage
58
Chengdu Gupte Biotechnology Co., Ltd.
Tel
13881890404
Fax
028-81711798
Email
2851503757@qq.com
Country
China
ProdList
2291
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
96815
Advantage
76
Meryer (Shanghai) Chemical Technology Co., Ltd.
Tel
021-61259108 18621169109
Fax
86-21-61259102
Email
market03@meryer.com
Country
China
ProdList
40240
Advantage
62
TCI (Shanghai) Development Co., Ltd.
Tel
021-67121386
Fax
021-67121385
Email
Sales-CN@TCIchemicals.com
Country
China
ProdList
24539
Advantage
81
BeiJing Hwrk Chemicals Limted
Tel
0757-86329057 18501085097
Fax
010-89508210
Email
sales3.gd@hwrkchemical.com
Country
China
ProdList
7639
Advantage
55
Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44751
Advantage
61
Sinopharm Chemical Reagent Co,Ltd.
Tel
86-21-63210123
Fax
86-21-63290778 86-21-63218885
Email
sj_scrc@sinopharm.com
Country
China
ProdList
9823
Advantage
79
ShangHai YuanYe Biotechnology Co., Ltd.
Tel
021-61312847 13636370518
Fax
021-55068248
Email
shyysw007@163.com
Country
China
ProdList
4941
Advantage
60
Chengdu Biopurify Phytochemicals Ltd.
Tel
+86-028-82633397 18982077548
Fax
+86-28-82633165
Email
cwb1@biopurify.cn
Country
China
ProdList
2376
Advantage
60
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Fax
010-65763397
Email
waley188@sohu.com
Country
China
ProdList
12338
Advantage
58
9ding chemical ( Shanghai) Limited
Tel
4009209199
Fax
86-021-52271987
Email
sales@9dingchem.com
Country
China
ProdList
22519
Advantage
55
Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
18521735133 18521732826;
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25014
Advantage
65
Shanghai Tauto Biotech Co., Ltd.
Tel
021-51320588
Fax
0086-21-51320502
Email
tauto@tautobiotech.com
Country
China
ProdList
3989
Advantage
66
Guangzhou Isun Pharmaceutical Co., Ltd
Tel
020-39119399 18927568969
Fax
020-39119999
Email
isunpharm@qq.com
Country
China
ProdList
4428
Advantage
55
TargetMol Chemicals Inc.
Tel
021-021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7854
Advantage
58
Shanghai TaoSu Biochemical Technology Co., Ltd.
Tel
021-33632979
Fax
021-34692979
Email
info@tsbiochem.com
Country
China
ProdList
8073
Advantage
58
Cheng Du Pufeide Biotechnology Co., Ltd.
Tel
028-82610909 13388174823
Fax
8171-1798
Email
scglp@glp-china.com
Country
China
ProdList
1064
Advantage
58
Bide Pharmatech Ltd.
Tel
400-1647117 15221909166
Fax
+86-21-61629029
Email
product02@bidepharm.com
Country
China
ProdList
41438
Advantage
60
Wuxi Zhongkun Biochemical Technology Co., Ltd.
Tel
0510-85629785 18013409632
Fax
051085625359
Email
sales@reading-chemicals.com
Country
China
ProdList
15185
Advantage
58
Shanghai Macklin Biochemical Co.,Ltd.
Tel
15221275939 15221275939
Fax
021-50706099
Email
shenlinxing@macklin.cn
Country
China
ProdList
15878
Advantage
55
Hangzhou J&H Chemical Co., Ltd.
Tel
+86-571-87396432
Fax
0571-87396431
Email
sales@jhechem.com
Country
China
ProdList
10015
Advantage
53
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51471
Advantage
80
Kono Chem Co.,Ltd
Tel
15829389671
Fax
029-86107037
Email
info@konochemical.com
Country
China
ProdList
554
Advantage
55
Wuhan ChemFaces Biochemical Co., Ltd.
Tel
18607101326 15172504745
Fax
+86-27-84254680
Email
aileen@chemfaces.com
Country
China
ProdList
7059
Advantage
55
Shanghai Synchem Pharma Co., ltd
Tel
021-61984905-1 18016477331
Email
synchempharma@aliyun.com
Country
China
ProdList
6455
Advantage
55
Pharmacodia (Beijing) Co.,Ltd
Tel
+86-400-851-9921
Fax
+86-10-82826195
Email
sales@pharmacodia.com
Country
China
ProdList
2317
Advantage
55
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9709
Advantage
58
Shandong Xiya Chemical Co., Ltd.
Tel
4009903999 13395398332
Fax
0539-6365991
Email
sales@xiyashiji.com
Country
China
ProdList
20810
Advantage
60
Chengdu Dianchun Technology Co., Ltd
Tel
400-1166-196 18502815961
Fax
QQ:800101999
Email
cdhxsj@163.com
Country
China
ProdList
14623
Advantage
60
Beijing Solarbio Science & Tecnology Co., Ltd.
Tel
010-50973130 4009686088
Email
3193328036@qq.com
Country
China
ProdList
29797
Advantage
68
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131981
Advantage
58
Beijing Jin Ming Biotechnology Co., Ltd.
Tel
010-60605840 18892239720
Fax
010-60605840
Email
psaitong@jm-bio.com
Country
China
ProdList
12308
Advantage
58
Shanghai Yihe Biological Technology Co., Ltd.
Tel
17721395025
Fax
021-68882955
Email
2423903095@qq.com
Country
China
ProdList
3153
Advantage
58
Hubei widely chemical technology Co., Ltd.
Tel
027-59402396 13419635609
Fax
027-83989310
Email
13419635609@163.com
Country
China
ProdList
1992
Advantage
55
Suzhou Laihui Biotechnology Co., Ltd.
Tel
180-13160973 +86-18013160973
Fax
0512-68236973
Email
rywaybio@gmail.com
Country
China
ProdList
296
Advantage
55
Shanghai Orgchem Co.,Ltd.
Tel
+86-21-5877 1921
Fax
+86-21-5877 1925
Email
info@chemofchina.com
Country
China
ProdList
9661
Advantage
55
Chengdu Push Bio-Technology Co., Ltd.
Tel
028-85370565-229 18080489829
Email
3004654993@qq.com
Country
China
ProdList
9174
Advantage
60
9ding chemical ( Shanghai) Limited
Tel
021-021-52271985 17721149837
Fax
+86 (21) 52271987
Email
sales@9dingchem.com
Country
China
ProdList
19806
Advantage
60
Chengdu Alfa Biotechnology Co.,Ltd.
Tel
028-85142057, 18030712385
Fax
028-85142057 QQ:3591697873
Email
sales@alfabiotech.com
Country
China
ProdList
1925
Advantage
58
Shanghai Standard Technology Co.,Ltd.
Tel
021-57127007-6622 15618937986
Fax
+86 (21) 5132-0077
Email
zhaok@nature-standard.com
Country
China
ProdList
3928
Advantage
58
Aikon International Limited
Tel
025-58859352 18068836627
Fax
02557626880
Email
sales01@aikonchem.com
Country
China
ProdList
15085
Advantage
58
Dishman Group
Tel
021-67121166-834
Fax
021-67121080
Email
sales.china@dishmangroup.com
Country
China
ProdList
106
Advantage
58
Tianjin heowns Biochemical Technology Co., Ltd.
Tel
400-6387771-6038 18902104717
Email
sales@heowns.com
Country
China
ProdList
20530
Advantage
60
Shanghai Tube Pharmaceutical Co., Ltd.
Tel
021-54338626 18017892860
Fax
021-54338626
Email
sales@tubepharm.com
Country
China
ProdList
2329
Advantage
58
Henan Alfachem Co.,Ltd.
Tel
0371-0371-55051623 18137891487
Fax
QQ:2853979817
Email
2853979817@qq.com
Country
China
ProdList
9962
Advantage
58
Shanghai Jizhi Biochemical Technology Co. Ltd.
Tel
400-400-400-9004166 18616739031
Email
3007523370@qq.com
Country
China
ProdList
52712
Advantage
58
Nanjing Digger Medical Technology Co. Ltd.
Tel
025-025-51191215 18013836722
Fax
025-51191215
Email
2399235533@qq.com
Country
China
ProdList
4933
Advantage
58
More
Less

View Lastest Price from LANOSTEROL manufacturers

Hebei Duling International Trade Co. LTD
Product
Lanosterol 79-63-0
Price
US $30.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
100 tons
Release date
2022-10-13
Wuhan Senwayer Century Chemical Co.,Ltd
Product
LANOSTEROL 79-63-0
Price
US $5500.00/kg
Min. Order
1kg
Purity
99%
Supply Ability
20 tons
Release date
2022-11-01
WUHAN FORTUNA CHEMICAL CO., LTD
Product
Lanosterol 79-63-0
Price
US $0.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
500kgs/month
Release date
2021-07-22

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