(4aS,10aS)-5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione

Details

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Internal ID bd963b4b-3851-4abd-9111-e1c719259a09
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aS,10aS)-5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H28O4/c1-11(2)12-9-13-14(22)10-15-20(3,4)16(23)7-8-21(15,5)17(13)18(24)19(12)25-6/h9,11,15,24H,7-8,10H2,1-6H3/t15-,21+/m1/s1
InChI Key YUGJHEXCGCZVTH-VFNWGFHPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H28O4
Molecular Weight 344.40 g/mol
Exact Mass 344.19875937 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 3.70
Atomic LogP (AlogP) 4.37
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4aS,10aS)-5-hydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9915 99.15%
Caco-2 + 0.7428 74.28%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.9029 90.29%
OATP2B1 inhibitior - 0.8610 86.10%
OATP1B1 inhibitior + 0.8743 87.43%
OATP1B3 inhibitior + 0.9282 92.82%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7033 70.33%
P-glycoprotein inhibitior - 0.8134 81.34%
P-glycoprotein substrate - 0.7392 73.92%
CYP3A4 substrate + 0.6413 64.13%
CYP2C9 substrate - 0.7515 75.15%
CYP2D6 substrate - 0.7145 71.45%
CYP3A4 inhibition + 0.5065 50.65%
CYP2C9 inhibition - 0.7844 78.44%
CYP2C19 inhibition - 0.7793 77.93%
CYP2D6 inhibition - 0.9362 93.62%
CYP1A2 inhibition + 0.7617 76.17%
CYP2C8 inhibition - 0.6058 60.58%
CYP inhibitory promiscuity - 0.9333 93.33%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8620 86.20%
Carcinogenicity (trinary) Non-required 0.6505 65.05%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.7719 77.19%
Skin irritation - 0.6163 61.63%
Skin corrosion - 0.9532 95.32%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6849 68.49%
Micronuclear - 0.8800 88.00%
Hepatotoxicity - 0.5584 55.84%
skin sensitisation - 0.9102 91.02%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.8448 84.48%
Acute Oral Toxicity (c) III 0.6256 62.56%
Estrogen receptor binding + 0.5835 58.35%
Androgen receptor binding - 0.5318 53.18%
Thyroid receptor binding + 0.6807 68.07%
Glucocorticoid receptor binding + 0.7081 70.81%
Aromatase binding - 0.5437 54.37%
PPAR gamma + 0.8254 82.54%
Honey bee toxicity - 0.7232 72.32%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9941 99.41%

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 98.72% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.66% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.75% 96.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 93.65% 99.15%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.64% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.90% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.78% 90.71%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.54% 82.69%
CHEMBL1937 Q92769 Histone deacetylase 2 89.33% 94.75%
CHEMBL1907 P15144 Aminopeptidase N 88.48% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.18% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.16% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.12% 94.00%
CHEMBL340 P08684 Cytochrome P450 3A4 87.99% 91.19%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.40% 86.33%
CHEMBL2535 P11166 Glucose transporter 86.89% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.32% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.87% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.66% 95.89%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.99% 96.77%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.68% 100.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 81.41% 93.03%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.25% 92.62%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 80.01% 92.88%

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.
Taxus mairei
Torreya nucifera

Cross-Links

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PubChem 163010400
LOTUS LTS0029143
wikiData Q105362861