(8alpha,10alpha)-9alpha,12alpha-Ethano-13-methylpodocarp-13-en-18-ol

Details

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Internal ID 63ca5486-fd6a-4bc4-9083-15cc9217e421
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Villanovane, atisane, trachylobane or helvifulvane diterpenoids > Stemarane diterpenoids
IUPAC Name [(1S,2R,6R,7R,10R,13S)-2,6,12-trimethyl-6-tetracyclo[11.2.1.01,10.02,7]hexadec-11-enyl]methanol
SMILES (Canonical) CC1=CC2CCC3C(CCCC3(C24CCC1C4)C)(C)CO
SMILES (Isomeric) CC1=C[C@H]2CC[C@H]3[C@](CCC[C@]3([C@]24CC[C@H]1C4)C)(C)CO
InChI InChI=1S/C20H32O/c1-14-11-16-5-6-17-18(2,13-21)8-4-9-19(17,3)20(16)10-7-15(14)12-20/h11,15-17,21H,4-10,12-13H2,1-3H3/t15-,16+,17-,18-,19+,20-/m0/s1
InChI Key TUSCOQSQOOTGAW-APNJTCTJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H32O
Molecular Weight 288.50 g/mol
Exact Mass 288.245315640 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.95
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (8alpha,10alpha)-9alpha,12alpha-Ethano-13-methylpodocarp-13-en-18-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9939 99.39%
Caco-2 + 0.9023 90.23%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.7741 77.41%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.7993 79.93%
OATP1B3 inhibitior + 0.8815 88.15%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.5813 58.13%
P-glycoprotein inhibitior - 0.8925 89.25%
P-glycoprotein substrate - 0.7857 78.57%
CYP3A4 substrate + 0.5723 57.23%
CYP2C9 substrate - 0.6016 60.16%
CYP2D6 substrate - 0.7472 74.72%
CYP3A4 inhibition - 0.7344 73.44%
CYP2C9 inhibition + 0.5304 53.04%
CYP2C19 inhibition - 0.5934 59.34%
CYP2D6 inhibition - 0.8772 87.72%
CYP1A2 inhibition - 0.7694 76.94%
CYP2C8 inhibition - 0.8001 80.01%
CYP inhibitory promiscuity - 0.5781 57.81%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.6246 62.46%
Eye corrosion - 0.9675 96.75%
Eye irritation - 0.8839 88.39%
Skin irritation - 0.7554 75.54%
Skin corrosion - 0.9675 96.75%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4790 47.90%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5299 52.99%
skin sensitisation + 0.5543 55.43%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7989 79.89%
Acute Oral Toxicity (c) III 0.7030 70.30%
Estrogen receptor binding + 0.8674 86.74%
Androgen receptor binding - 0.5421 54.21%
Thyroid receptor binding + 0.6470 64.70%
Glucocorticoid receptor binding + 0.8144 81.44%
Aromatase binding + 0.7353 73.53%
PPAR gamma - 0.6459 64.59%
Honey bee toxicity - 0.9403 94.03%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9918 99.18%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.80% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.80% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.34% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.73% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 89.15% 94.75%
CHEMBL2581 P07339 Cathepsin D 86.97% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.04% 82.69%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.54% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.83% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.02% 95.89%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.70% 95.50%

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.
Calceolaria lepida
Euphorbia maculata

Cross-Links

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PubChem 101615210
NPASS NPC61162
LOTUS LTS0238357
wikiData Q105264991