(4aR)-6-hydroxy-5-methoxy-1,1,4a,7-tetramethyl-3,4-dihydrophenanthrene-2,9-dione

Details

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Internal ID 35a0536b-357d-422d-ad62-bad30a1e2413
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aR)-6-hydroxy-5-methoxy-1,1,4a,7-tetramethyl-3,4-dihydrophenanthrene-2,9-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H22O4/c1-10-8-11-12(20)9-13-18(2,3)14(21)6-7-19(13,4)15(11)17(23-5)16(10)22/h8-9,22H,6-7H2,1-5H3/t19-/m1/s1
InChI Key KSIDTNCNAIUBCC-LJQANCHMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H22O4
Molecular Weight 314.40 g/mol
Exact Mass 314.15180918 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.48
H-Bond Acceptor 4
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 (4aR)-6-hydroxy-5-methoxy-1,1,4a,7-tetramethyl-3,4-dihydrophenanthrene-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 + 0.9971 99.71%
Caco-2 + 0.7769 77.69%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.8275 82.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8748 87.48%
OATP1B3 inhibitior + 0.9247 92.47%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6227 62.27%
P-glycoprotein inhibitior - 0.8909 89.09%
P-glycoprotein substrate - 0.8649 86.49%
CYP3A4 substrate + 0.6119 61.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7710 77.10%
CYP3A4 inhibition - 0.5282 52.82%
CYP2C9 inhibition - 0.5222 52.22%
CYP2C19 inhibition - 0.5135 51.35%
CYP2D6 inhibition - 0.7864 78.64%
CYP1A2 inhibition + 0.6998 69.98%
CYP2C8 inhibition + 0.4696 46.96%
CYP inhibitory promiscuity - 0.7447 74.47%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9081 90.81%
Carcinogenicity (trinary) Non-required 0.6084 60.84%
Eye corrosion - 0.9925 99.25%
Eye irritation + 0.7316 73.16%
Skin irritation - 0.6372 63.72%
Skin corrosion - 0.9511 95.11%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7261 72.61%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5629 56.29%
skin sensitisation - 0.7296 72.96%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.7388 73.88%
Acute Oral Toxicity (c) III 0.6308 63.08%
Estrogen receptor binding + 0.6451 64.51%
Androgen receptor binding + 0.5583 55.83%
Thyroid receptor binding + 0.5829 58.29%
Glucocorticoid receptor binding + 0.6467 64.67%
Aromatase binding - 0.5919 59.19%
PPAR gamma + 0.6082 60.82%
Honey bee toxicity - 0.9184 91.84%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9920 99.20%

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 98.29% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.85% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 92.97% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.77% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.75% 86.33%
CHEMBL2581 P07339 Cathepsin D 91.55% 98.95%
CHEMBL2535 P11166 Glucose transporter 88.90% 98.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 88.83% 93.99%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.75% 99.15%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.36% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.00% 96.09%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 83.72% 82.38%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 82.74% 96.67%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.61% 91.07%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.43% 89.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.15% 92.94%
CHEMBL1907 P15144 Aminopeptidase N 81.51% 93.31%
CHEMBL1871 P10275 Androgen Receptor 81.12% 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.
Drypetes littoralis

Cross-Links

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PubChem 10881566
LOTUS LTS0259652
wikiData Q105145422