(1R,4R,5R,8R,10R,13R,14R,17R,18R,19S)-10-hydroxy-4,5,9,9,13-pentamethyl-19-prop-1-en-2-yl-20-oxahexacyclo[17.2.2.01,18.04,17.05,14.08,13]tricosan-21-one

Details

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Internal ID d469a207-7b1b-4421-9d75-2be210fe18b2
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1R,4R,5R,8R,10R,13R,14R,17R,18R,19S)-10-hydroxy-4,5,9,9,13-pentamethyl-19-prop-1-en-2-yl-20-oxahexacyclo[17.2.2.01,18.04,17.05,14.08,13]tricosan-21-one
SMILES (Canonical) CC(=C)C12CCC3(C1C4CCC5C6(CCC(C(C6CCC5(C4(CC3)C)C)(C)C)O)C)C(=O)O2
SMILES (Isomeric) CC(=C)[C@]12CC[C@]3([C@H]1[C@H]4CC[C@@H]5[C@]6(CC[C@H](C([C@@H]6CC[C@]5([C@@]4(CC3)C)C)(C)C)O)C)C(=O)O2
InChI InChI=1S/C30H46O3/c1-18(2)30-17-16-29(24(32)33-30)15-14-27(6)19(23(29)30)8-9-21-26(5)12-11-22(31)25(3,4)20(26)10-13-28(21,27)7/h19-23,31H,1,8-17H2,2-7H3/t19-,20+,21-,22-,23-,26+,27-,28-,29-,30-/m1/s1
InChI Key IBPHOZYTFQMNIJ-RJTIZZONSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H46O3
Molecular Weight 454.70 g/mol
Exact Mass 454.34469533 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 7.70

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,4R,5R,8R,10R,13R,14R,17R,18R,19S)-10-hydroxy-4,5,9,9,13-pentamethyl-19-prop-1-en-2-yl-20-oxahexacyclo[17.2.2.01,18.04,17.05,14.08,13]tricosan-21-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
No predicted properties yet!

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.63% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.59% 91.11%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.11% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.34% 100.00%
CHEMBL218 P21554 Cannabinoid CB1 receptor 86.62% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.46% 95.89%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.33% 96.09%
CHEMBL2581 P07339 Cathepsin D 85.44% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.32% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.12% 97.09%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.09% 97.14%
CHEMBL1871 P10275 Androgen Receptor 80.31% 96.43%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Microtropis fokienensis

Cross-Links

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PubChem 25017711
LOTUS LTS0103333
wikiData Q105036600