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Home Other Building Blocks Lanost-8-en-21-oic acid, 3-(acetyloxy)-16-hydroxy-24-methylene-, (3β,16α)-

Lanost-8-en-21-oic acid, 3-(acetyloxy)-16-hydroxy-24-methylene-, (3β,16α)-

CAS No.:
29070-92-6
Catalog Number:
AG002X86
Molecular Formula:
C33H52O5
Molecular Weight:
528.7630
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1mg
98%(HPLC)powder
In Stock USA
United States
$151
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5mg
98%(HPLC)powder
In Stock USA
United States
$319
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10mg
98%(HPLC)powder
In Stock USA
United States
$486
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25mg
98%(HPLC)powder
In Stock USA
United States
$782
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50mg
98%(HPLC)powder
In Stock USA
United States
$1486
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Product Description
Catalog Number:
AG002X86
Chemical Name:
Lanost-8-en-21-oic acid, 3-(acetyloxy)-16-hydroxy-24-methylene-, (3β,16α)-
CAS Number:
29070-92-6
Molecular Formula:
C33H52O5
Molecular Weight:
528.7630
MDL Number:
MFCD00238657
IUPAC Name:
(2R)-2-[(3S,5R,10S,13R,14R,16R,17R)-3-acetyloxy-16-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methyl-5-methylideneheptanoic acid
InChI:
InChI=1S/C33H52O5/c1-19(2)20(3)10-11-22(29(36)37)28-25(35)18-33(9)24-12-13-26-30(5,6)27(38-21(4)34)15-16-31(26,7)23(24)14-17-32(28,33)8/h19,22,25-28,35H,3,10-18H2,1-2,4-9H3,(H,36,37)/t22-,25-,26+,27+,28+,31-,32-,33+/m1/s1
InChI Key:
VDYCLYGKCGVBHN-DRCQUEPLSA-N
SMILES:
CC(=O)O[C@H]1CC[C@]2([C@H](C1(C)C)CCC1=C2CC[C@]2([C@@]1(C)C[C@H]([C@@H]2[C@H](C(=O)O)CCC(=C)C(C)C)O)C)C
UNII:
X2FCK16QAH
Properties
Complexity:
1020  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
8  
Defined Bond Stereocenter Count:
0
Exact Mass:
528.381g/mol
Formal Charge:
0
Heavy Atom Count:
38  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
528.774g/mol
Monoisotopic Mass:
528.381g/mol
Rotatable Bond Count:
8  
Topological Polar Surface Area:
83.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
7.2  
Literature
Title Journal
Role of RAS/Wnt/β-catenin axis activation in the pathogenesis of podocyte injury and tubulo-interstitial nephropathy. Chemico-biological interactions 20170801
Pachymic acid stimulates glucose uptake through enhanced GLUT4 expression and translocation. European journal of pharmacology 20101201
[RP-HPLC simultaneous determination of five triterpenoid acids in different parts of Poria cocos by UV wavelengths switch]. Yao xue xue bao = Acta pharmaceutica Sinica 20100401
Pachymic acid inhibits cell growth and modulates arachidonic acid metabolism in nonsmall cell lung cancer A549 cells. Molecular carcinogenesis 20100301
Effects of triterpenoids from Poria cocos Wolf on the serotonin type 3A receptor-mediated ion current in Xenopus oocytes. European journal of pharmacology 20090801
Absorption and transport of pachymic acid in the human intestinal cell line Caco-2 monolayers. Zhong xi yi jie he xue bao = Journal of Chinese integrative medicine 20080701
Triterpene acids from Poria cocos and their anti-tumor-promoting effects. Journal of natural products 20070601
Induction of apoptosis in prostate cancer cells by pachymic acid from Poria cocos. Biochemical and biophysical research communications 20050715
Inhibitory effects of triterpenes isolated from Hoelen on free radical-induced lysis of red blood cells. Phytotherapy research : PTR 20030201
Properties