InChI=1S/C29H48O2/c1-7-20(18(2)3)16-27(31)19(4)24-10-11-25-23-9-8-21-17-22(30)12-14-28(21,5)26(23)13-15-29(24,25)6/h17-20,23-27,31H,7-16H2,1-6H3/t19-,20+,23-,24+,25-,26-,27+,28-,29+/m0/s1 |
LXRLKMAYPPIRJM-GACZPLPESA-N |
[H][C@@]1(CC[C@@]2([H])[C@]3([H])CCC4=CC(=O)CC[C@]4(C)[C@@]3([H])CC[C@]12C)[C@H](C)[C@H](O)C[C@@H](CC)C(C)C |
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Haloxylon recurvum
(IPNI:165851-1)
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Found in
whole plant
(BTO:0001461).
See:
PubMed
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EC 3.4.21.1 (chymotrypsin) inhibitor
An EC 3.4.21.* (serine endopeptidase) inhibitor that interferes with the action of chymotrypsin (EC 3.4.21.1).
metabolite
Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
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View more via ChEBI Ontology
(22R)-22-hydroxystigmast-4-en-3-one
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(22R,24R)-24-ethyl-3-oxo-cholest-4-ene-22-ol
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ChEBI
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10397682
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Reaxys Registry Number
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Reaxys
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Hussain S, Ahmed E, Malik A, Jabbar A, Ashraf M, Lodhi MA, Choudhary MI (2006) Halosterols A and B, chymotrypsin inhibitory sterols from Haloxylon recurvum. Chemical & pharmaceutical bulletin 54, 623-625 [PubMed:16651755] [show Abstract] Two new sterols, halosterols A (1) and B (2), have been isolated from the CHCl(3) soluble fraction of Haloxylon recurvum, and their structures were elucidated by spectroscopic techniques including two dimensional-NMR. Both the compounds displayed chymotrypsin enzyme inhibitory potential. |
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