Taiwaniaquinone G

Details

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Internal ID f37d59bc-cfa0-4cd8-bd31-9a8fe98c7295
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4bS,8aS)-3-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7,8a,9-tetrahydro-5H-fluorene-1,4-dione
SMILES (Canonical) CC(C)C1=C(C(=O)C2=C(C1=O)CC3C2(CCCC3(C)C)C)OC
SMILES (Isomeric) CC(C)C1=C(C(=O)C2=C(C1=O)C[C@@H]3[C@@]2(CCCC3(C)C)C)OC
InChI InChI=1S/C20H28O3/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/h11,13H,7-10H2,1-6H3/t13-,20-/m0/s1
InChI Key AVTKDJHUFWOONG-RBZFPXEDSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O3
Molecular Weight 316.40 g/mol
Exact Mass 316.20384475 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.23
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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CHEMBL1088628
(4bS,8aS)-3-methoxy-4b,8,8-trimethyl-2-propan-2-yl-6,7,8a,9-tetrahydro-5H-fluorene-1,4-dione

2D Structure

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2D Structure of Taiwaniaquinone G

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 + 0.8296 82.96%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.8047 80.47%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.9196 91.96%
OATP1B3 inhibitior + 0.9691 96.91%
MATE1 inhibitior - 0.6400 64.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior - 0.7410 74.10%
P-glycoprotein inhibitior - 0.6480 64.80%
P-glycoprotein substrate - 0.8797 87.97%
CYP3A4 substrate + 0.5814 58.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8564 85.64%
CYP3A4 inhibition - 0.8796 87.96%
CYP2C9 inhibition - 0.6201 62.01%
CYP2C19 inhibition - 0.6176 61.76%
CYP2D6 inhibition - 0.9431 94.31%
CYP1A2 inhibition - 0.7447 74.47%
CYP2C8 inhibition - 0.8093 80.93%
CYP inhibitory promiscuity - 0.7458 74.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9620 96.20%
Carcinogenicity (trinary) Non-required 0.4812 48.12%
Eye corrosion - 0.9877 98.77%
Eye irritation - 0.7770 77.70%
Skin irritation - 0.5824 58.24%
Skin corrosion - 0.9623 96.23%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4713 47.13%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.5959 59.59%
skin sensitisation - 0.6324 63.24%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity + 0.4943 49.43%
Acute Oral Toxicity (c) III 0.5438 54.38%
Estrogen receptor binding + 0.5714 57.14%
Androgen receptor binding - 0.5151 51.51%
Thyroid receptor binding + 0.6535 65.35%
Glucocorticoid receptor binding - 0.4916 49.16%
Aromatase binding - 0.7520 75.20%
PPAR gamma + 0.6182 61.82%
Honey bee toxicity - 0.7179 71.79%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5900 59.00%
Fish aquatic toxicity + 0.9961 99.61%

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 96.17% 97.25%
CHEMBL2581 P07339 Cathepsin D 94.75% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.42% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.08% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.11% 94.45%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.74% 82.69%
CHEMBL1937 Q92769 Histone deacetylase 2 91.02% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.84% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.92% 96.77%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.38% 97.14%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 89.30% 96.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.84% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.95% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.89% 91.07%
CHEMBL2996 Q05655 Protein kinase C delta 81.67% 97.79%

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 25199270
NPASS NPC23778
LOTUS LTS0034469
wikiData Q104919825