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About This Item
Empirical Formula (Hill Notation):
C27H44O
CAS Number:
Molecular Weight:
384.64
UNSPSC Code:
12352115
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-005-1
Beilstein/REAXYS Number:
2224119
MDL number:
Assay:
98%
Form:
solid
assay
98%
form
solid
optical activity
[α]23/D +91.0°, c = 2 in chloroform
mp
79-81 °C (lit.)
functional group
ketone
SMILES string
[H][C@@]12[C@]([C@](CC3)(C)C(CC2)=CC3=O)([H])CC[C@@]4(C)[C@@]1([H])CC[C@]4([H])[C@]([H])(C)CCCC(C)C
InChI
1S/C27H44O/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28)13-15-26(20,4)25(22)14-16-27(23,24)5/h17-19,22-25H,6-16H2,1-5H3/t19-,22+,23-,24+,25+,26+,27-/m1/s1
InChI key
NYOXRYYXRWJDKP-GYKMGIIDSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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G Tibolla et al.
Atherosclerosis, 210(1), 78-87 (2009-12-01)
Atherosclerosis is associated with Alzheimer's disease (AD) in humans, but the nature of this link is still elusive. Aim of this study was to investigate aortic atherosclerosis development in a mouse model with central nervous system (CNS) restricted beta-amyloid precursor
Satoshi Yamaguchi et al.
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A chemically-activatable alkynyl steroid analogue probe has been synthesized for visualizing the lipid raft membrane domains by Raman microscopy. The Raman probe, in which ring A of its steroid backbone is replaced with an alkynyl group, was designed to enable