CHEBI:90931 - NCS172285

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ChEBI Name NCS172285
ChEBI ID CHEBI:90931
Definition A 3β-hydroxy steroid that is androst-5-en-3β-ol in which the 17β-hydrogen has been replaced by a 1,3-dihydroxy-3,3-bis(trifluoromethyl)propyl group. NCS172285 (also known as acts as NSC12) has been used as an extracellular fibroblast growth factor (FGF) trap with implications in cancer therapy. The stereochemistry shown is that of the most active stereoisomer, as determined by Mattia Anselmi (PhD thesis, University of Parma, 2015).
Stars This entity has been manually annotated by the ChEBI Team.
Submitter Margaret Duesbury
Supplier Information
Download Molfile XML SDF
Formula C24H34F6O3
Net Charge 0
Average Mass 484.516
Monoisotopic Mass 484.24121
InChI InChI=1S/C24H34F6O3/c1-20-9-7-14(31)11-13(20)3-4-15-16-5-6-18(21(16,2)10-8-17(15)20)19(32)12-22(33,23(25,26)27)24(28,29)30/h3,14-19,31-33H,4-12H2,1-2H3/t14-,15-,16-,17-,18+,19-,20-,21-/m0/s1
InChIKey OHKBOEWLASAFLW-FJWDNACWSA-N
SMILES [C@@H](CC(O)(C(F)(F)F)C(F)(F)F)(O)[C@@]1([C@]2(CC[C@@]3([C@]4(CC[C@@H](CC4=CC[C@]3([C@@]2(CC1)[H])[H])O)C)[H])C)[H]
ChEBI Ontology
Outgoing NCS172285 (CHEBI:90931) is a 20-hydroxy steroid (CHEBI:36854)
NCS172285 (CHEBI:90931) is a 3β-hydroxy-Δ5-steroid (CHEBI:1722)
NCS172285 (CHEBI:90931) is a fluorinated steroid (CHEBI:50830)
Synonyms Sources
(1S)-4,4,4-trifluoro-1-[(3S,8S,9S,10R,13S,14S,17S)-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-3-(trifluoromethyl)butane-1,3-diol IUPAC
(20S)-21-[hydroxy(bistrifluoromethyl)methyl]pregnane-3β,20-diol ChEBI
17β-[(1S)-1,3-dihydroxy-3,3-bis(trifluoromethyl)propyl] androst-5-en-3β-ol ChEBI
17β-[(1S)-4,4,4-trifluoro-1,3-dihydroxy-3-(trifluoromethyl)butyl] androst-5-en-3β-ol ChEBI
NSC12 ChEBI
UPR1358 ChEBI
Citation Waiting for Citations Type Source
26267536 PubMed citation SUBMITTER
Last Modified
25 April 2017
General Comment
2016-01-15 The stereochemistry shown is as determined by Mattia Anselmi (PhD thesis, chapter 4. See http://dspace-unipr.cineca.it/bitstream/1889/2765/1/PhDThesis_final.pdf)