7-hydroxy-6-methoxy-1,1,4a-trimethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one

Details

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Internal ID b75b4324-f97a-4b26-ba80-70f10d1d2adb
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name 7-hydroxy-6-methoxy-1,1,4a-trimethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one
SMILES (Canonical) CC1(C2CCC3=CC(=C(C=C3C2(CCC1=O)C)OC)O)C
SMILES (Isomeric) CC1(C2CCC3=CC(=C(C=C3C2(CCC1=O)C)OC)O)C
InChI InChI=1S/C18H24O3/c1-17(2)15-6-5-11-9-13(19)14(21-4)10-12(11)18(15,3)8-7-16(17)20/h9-10,15,19H,5-8H2,1-4H3
InChI Key OCGQUJKSKBOSPQ-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H24O3
Molecular Weight 288.40 g/mol
Exact Mass 288.17254462 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.61
H-Bond Acceptor 3
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 7-hydroxy-6-methoxy-1,1,4a-trimethyl-4,9,10,10a-tetrahydro-3H-phenanthren-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.8624 86.24%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.8979 89.79%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.9190 91.90%
OATP1B3 inhibitior + 0.9685 96.85%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.5234 52.34%
P-glycoprotein inhibitior - 0.7706 77.06%
P-glycoprotein substrate - 0.8696 86.96%
CYP3A4 substrate + 0.6107 61.07%
CYP2C9 substrate - 0.6950 69.50%
CYP2D6 substrate + 0.3657 36.57%
CYP3A4 inhibition - 0.6214 62.14%
CYP2C9 inhibition - 0.6908 69.08%
CYP2C19 inhibition - 0.6421 64.21%
CYP2D6 inhibition - 0.9335 93.35%
CYP1A2 inhibition + 0.7659 76.59%
CYP2C8 inhibition + 0.4577 45.77%
CYP inhibitory promiscuity - 0.8973 89.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8520 85.20%
Carcinogenicity (trinary) Non-required 0.5878 58.78%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.7350 73.50%
Skin irritation - 0.5805 58.05%
Skin corrosion - 0.9594 95.94%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5232 52.32%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.8883 88.83%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.7889 78.89%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6716 67.16%
Acute Oral Toxicity (c) III 0.6507 65.07%
Estrogen receptor binding + 0.6984 69.84%
Androgen receptor binding - 0.6573 65.73%
Thyroid receptor binding + 0.7135 71.35%
Glucocorticoid receptor binding + 0.7607 76.07%
Aromatase binding - 0.5104 51.04%
PPAR gamma + 0.7528 75.28%
Honey bee toxicity - 0.7879 78.79%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5649 56.49%
Fish aquatic toxicity + 0.9897 98.97%

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 98.56% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.83% 96.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 94.54% 92.94%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.10% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 91.18% 94.75%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.42% 82.69%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.24% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.21% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.97% 94.45%
CHEMBL2535 P11166 Glucose transporter 85.39% 98.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.72% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.57% 93.99%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.34% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.97% 92.62%
CHEMBL2581 P07339 Cathepsin D 83.86% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 83.19% 91.19%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.10% 93.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.13% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 81.59% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.01% 85.14%

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.
Taiwania cryptomerioides

Cross-Links

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PubChem 74076280
LOTUS LTS0004171
wikiData Q105189352