(5R,9R,10R,13S,14S,17S)-17-[(E,2S)-4-[(2S)-3,3-dimethyloxiran-2-yl]but-3-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one

Details

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Internal ID 22215f94-3e9d-4c95-8c8c-7853e1de5ab4
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (5R,9R,10R,13S,14S,17S)-17-[(E,2S)-4-[(2S)-3,3-dimethyloxiran-2-yl]but-3-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one
SMILES (Canonical) CC(C=CC1C(O1)(C)C)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C
SMILES (Isomeric) C[C@@H](/C=C/[C@H]1C(O1)(C)C)[C@@H]2CC[C@]3([C@]2(CC[C@H]4C3=CC[C@@H]5[C@@]4(CCC(=O)C5(C)C)C)C)C
InChI InChI=1S/C30H46O2/c1-19(9-12-25-27(4,5)32-25)20-13-17-30(8)22-10-11-23-26(2,3)24(31)15-16-28(23,6)21(22)14-18-29(20,30)7/h9-10,12,19-21,23,25H,11,13-18H2,1-8H3/b12-9+/t19-,20-,21-,23-,25-,28+,29-,30+/m0/s1
InChI Key NHJZKKCNKMFNLM-VRWWYAQOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C30H46O2
Molecular Weight 438.70 g/mol
Exact Mass 438.349780706 g/mol
Topological Polar Surface Area (TPSA) 29.60 Ų
XlogP 7.00
Atomic LogP (AlogP) 7.53
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (5R,9R,10R,13S,14S,17S)-17-[(E,2S)-4-[(2S)-3,3-dimethyloxiran-2-yl]but-3-en-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5683 56.83%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5715 57.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8797 87.97%
OATP1B3 inhibitior + 0.9806 98.06%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 0.9206 92.06%
P-glycoprotein inhibitior + 0.6564 65.64%
P-glycoprotein substrate - 0.6951 69.51%
CYP3A4 substrate + 0.6434 64.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8110 81.10%
CYP3A4 inhibition - 0.8341 83.41%
CYP2C9 inhibition - 0.8022 80.22%
CYP2C19 inhibition + 0.5706 57.06%
CYP2D6 inhibition - 0.9394 93.94%
CYP1A2 inhibition - 0.5484 54.84%
CYP2C8 inhibition + 0.5123 51.23%
CYP inhibitory promiscuity - 0.7511 75.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5204 52.04%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.9501 95.01%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9550 95.50%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6555 65.55%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.5790 57.90%
skin sensitisation + 0.6071 60.71%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5416 54.16%
Acute Oral Toxicity (c) III 0.7498 74.98%
Estrogen receptor binding + 0.7914 79.14%
Androgen receptor binding + 0.7333 73.33%
Thyroid receptor binding + 0.7345 73.45%
Glucocorticoid receptor binding + 0.7944 79.44%
Aromatase binding + 0.6171 61.71%
PPAR gamma + 0.6486 64.86%
Honey bee toxicity - 0.7400 74.00%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9859 98.59%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.77% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.89% 95.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 90.73% 85.30%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.66% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.89% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.97% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.93% 97.25%
CHEMBL2581 P07339 Cathepsin D 85.92% 98.95%
CHEMBL1937 Q92769 Histone deacetylase 2 85.79% 94.75%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.96% 90.71%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.19% 99.23%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 83.31% 82.69%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 83.25% 85.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.85% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.57% 95.89%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 80.78% 96.77%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.21% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.07% 94.45%

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.
Toona ciliata

Cross-Links

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PubChem 15507873
LOTUS LTS0086337
wikiData Q104400691