Name: Name:Ergosta-5,22-dien-3-ol, (3b,22E)-
Brand: Angene
SKU: AG01CC9V
Rating: 90 (10 reviews)

Catalog Number:

AG01CC9V

Chemical Name:

Ergosta-5,22-dien-3-ol, (3b,22E)-

CAS Number:

474-67-9

Molecular Formula:

C28H46O

Molecular Weight:

398.6642

MDL Number:

MFCD00201659

IUPAC Name:

(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol

InChI:

InChI=1S/C28H46O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h7-9,18-20,22-26,29H,10-17H2,1-6H3/b8-7+/t19-,20+,22-,23-,24+,25-,26-,27-,28+/m0/s1

InChI Key:

OILXMJHPFNGGTO-ZAUYPBDWSA-N

SMILES:

O[C@H]1CC[C@]2(C(=CC[C@@H]3[C@@H]2CC[C@]2([C@H]3CC[C@@H]2[C@@H](/C=C/[C@@H](C(C)C)C)C)C)C1)C

EC Number:

207-486-5

UNII:

2B0KG2XFOF

Complexity:

659

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

398.355g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

398.675g/mol

Monoisotopic Mass:

398.355g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

20.2A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

Title	Journal
An ultra performance liquid chromatographic method for determining phytosterol uptake by Caco-2 cells.	Analytical biochemistry 20120201
Soyasapogenol B and trans-22-dehydrocam- pesterol from common vetch (Vicia sativa L.) root exudates stimulate broomrape seed germination.	Pest management science 20110801
Cloning, mechanistic and functional analysis of a fungal sterol C24-methyltransferase implicated in brassicasterol biosynthesis.	Biochimica et biophysica acta 20101001
Effect of rapeseed oil-derived plant sterol and stanol esters on atherosclerosis parameters in cholesterol-challenged heterozygous Watanabe heritable hyperlipidaemic rabbits.	The British journal of nutrition 20091201
Phytosterols accumulation in the seeds of Linum usitatissimum L.	Plant physiology and biochemistry : PPB 20091001
Dietary phytosterols and phytostanols alter the expression of sterol-regulatory genes in SHRSP and WKY inbred rats.	Annals of nutrition & metabolism 20090101
Inhibition of cholesterol transport into skin cells in cultures by phytosterol-loaded microemulsion.	Chemistry and physics of lipids 20080601
[Study on the sterols from a brown alga endophytic fungus (NO. ZZF36) from the South China Sea].	Zhong yao cai = Zhongyaocai = Journal of Chinese medicinal materials 20060901
Solubility in and affinity for the bile salt micelle of plant sterols are important determinants of their intestinal absorption in rats.	Lipids 20060601
Nystatin-induced lipid vesicles permeabilization is strongly dependent on sterol structure.	Biochimica et biophysica acta 20060401
Ganoderma total sterol (GS) and GS1 protect rat cerebral cortical neurons from hypoxia/reoxygenation injury.	Life sciences 20050114
Rapid quantification of free and esterified phytosterols in human serum using APPI-LC-MS/MS.	Journal of lipid research 20050101
Contribution of lipoxygenase metabolism to the brassinosteroid signaling pathway.	Doklady. Biochemistry and biophysics 20040101
Sterol composition of gonad, muscle and digestive gland of Pecten maximus from Málaga (South Spain).	Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology 20030301
The ratio of campesterol to sitosterol that modulates growth in Arabidopsis is controlled by STEROL METHYLTRANSFERASE 2;1.	The Plant journal : for cell and molecular biology 20010301
Plants steroid hormones, brassinosteroids: current highlights of molecular aspects on their synthesis/metabolism, transport, perception and response.	Plant & cell physiology 20010201
Definitive structural identities of 42 sterol components in Pneumocystis carinii.	The Journal of eukaryotic microbiology 20010101