Taiwaniaquinone H

Details

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Internal ID 2a082765-4dca-4da9-b9dd-73d468acfc9e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4bS)-3-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7-dihydro-5H-fluorene-1,4-dione
SMILES (Canonical) CC(C)C1=C(C(=O)C2=C(C1=O)C=C3C2(CCCC3(C)C)C)OC
SMILES (Isomeric) CC(C)C1=C(C(=O)C2=C(C1=O)C=C3[C@@]2(CCCC3(C)C)C)OC
InChI InChI=1S/C20H26O3/c1-11(2)14-16(21)12-10-13-19(3,4)8-7-9-20(13,5)15(12)17(22)18(14)23-6/h10-11H,7-9H2,1-6H3/t20-/m0/s1
InChI Key LEXZEULYIQDNCX-FQEVSTJZSA-N
Popularity 13 references in papers

Physical and Chemical Properties

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Molecular Formula C20H26O3
Molecular Weight 314.40 g/mol
Exact Mass 314.18819469 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 4.60
Atomic LogP (AlogP) 4.15
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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(-)-Taiwaniaquinone H
CHEMBL1077114

2D Structure

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2D Structure of Taiwaniaquinone H

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 + 0.7748 77.48%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.7756 77.56%
OATP2B1 inhibitior - 0.8576 85.76%
OATP1B1 inhibitior + 0.9165 91.65%
OATP1B3 inhibitior + 0.9608 96.08%
MATE1 inhibitior - 0.6400 64.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8050 80.50%
P-glycoprotein inhibitior - 0.7481 74.81%
P-glycoprotein substrate - 0.8446 84.46%
CYP3A4 substrate + 0.5524 55.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8564 85.64%
CYP3A4 inhibition - 0.9110 91.10%
CYP2C9 inhibition - 0.6362 63.62%
CYP2C19 inhibition - 0.6430 64.30%
CYP2D6 inhibition - 0.9267 92.67%
CYP1A2 inhibition - 0.6767 67.67%
CYP2C8 inhibition - 0.8662 86.62%
CYP inhibitory promiscuity - 0.7107 71.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9520 95.20%
Carcinogenicity (trinary) Non-required 0.4692 46.92%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.7516 75.16%
Skin irritation - 0.5671 56.71%
Skin corrosion - 0.9499 94.99%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6051 60.51%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.5144 51.44%
skin sensitisation - 0.5844 58.44%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.6142 61.42%
Acute Oral Toxicity (c) III 0.6058 60.58%
Estrogen receptor binding + 0.5496 54.96%
Androgen receptor binding + 0.5969 59.69%
Thyroid receptor binding + 0.6810 68.10%
Glucocorticoid receptor binding - 0.5501 55.01%
Aromatase binding - 0.6768 67.68%
PPAR gamma + 0.7236 72.36%
Honey bee toxicity - 0.7442 74.42%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9902 99.02%

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 96.81% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.77% 97.25%
CHEMBL2581 P07339 Cathepsin D 96.27% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.88% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 92.39% 94.75%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.41% 93.99%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.03% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.34% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.27% 82.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.37% 94.45%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.55% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.01% 95.89%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 81.79% 85.30%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.51% 99.23%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.24% 91.07%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.97% 96.67%

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 44597340
NPASS NPC283087
LOTUS LTS0247086
wikiData Q105150882