Taiwaniaquinol E

Details

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Internal ID 0902555b-e61c-450b-bbf7-a1ea82db30ab
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (4aS,9aS)-5,8-dihydroxy-6-methoxy-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9a-tetrahydrofluoren-9-one
SMILES (Canonical) CC(C)C1=C(C2=C(C(=C1OC)O)C3(CCCC(C3C2=O)(C)C)C)O
SMILES (Isomeric) CC(C)C1=C(C2=C(C(=C1OC)O)[C@]3(CCCC([C@@H]3C2=O)(C)C)C)O
InChI InChI=1S/C20H28O4/c1-10(2)11-14(21)12-13(16(23)17(11)24-6)20(5)9-7-8-19(3,4)18(20)15(12)22/h10,18,21,23H,7-9H2,1-6H3/t18-,20+/m0/s1
InChI Key PZLPUCMOBKVMOI-AZUAARDMSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C20H28O4
Molecular Weight 332.40 g/mol
Exact Mass 332.19875937 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.51
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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CHEMBL1088043

2D Structure

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2D Structure of Taiwaniaquinol E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.6505 65.05%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.8127 81.27%
OATP2B1 inhibitior - 0.8552 85.52%
OATP1B1 inhibitior + 0.8311 83.11%
OATP1B3 inhibitior + 0.9332 93.32%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.8984 89.84%
P-glycoprotein inhibitior - 0.8177 81.77%
P-glycoprotein substrate - 0.8374 83.74%
CYP3A4 substrate + 0.6110 61.10%
CYP2C9 substrate - 0.7891 78.91%
CYP2D6 substrate - 0.7955 79.55%
CYP3A4 inhibition - 0.8202 82.02%
CYP2C9 inhibition - 0.6008 60.08%
CYP2C19 inhibition - 0.6158 61.58%
CYP2D6 inhibition - 0.9041 90.41%
CYP1A2 inhibition + 0.8910 89.10%
CYP2C8 inhibition - 0.8097 80.97%
CYP inhibitory promiscuity - 0.7258 72.58%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8620 86.20%
Carcinogenicity (trinary) Non-required 0.5664 56.64%
Eye corrosion - 0.9902 99.02%
Eye irritation + 0.5663 56.63%
Skin irritation - 0.5901 59.01%
Skin corrosion - 0.9395 93.95%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5818 58.18%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.5754 57.54%
skin sensitisation - 0.8659 86.59%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.6766 67.66%
Acute Oral Toxicity (c) III 0.5727 57.27%
Estrogen receptor binding + 0.7398 73.98%
Androgen receptor binding - 0.5692 56.92%
Thyroid receptor binding + 0.6901 69.01%
Glucocorticoid receptor binding + 0.7335 73.35%
Aromatase binding + 0.5268 52.68%
PPAR gamma + 0.6910 69.10%
Honey bee toxicity - 0.8093 80.93%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9907 99.07%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.91% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.66% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.70% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.38% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.29% 97.25%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 90.01% 99.15%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.90% 95.56%
CHEMBL1937 Q92769 Histone deacetylase 2 89.19% 94.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 87.73% 96.77%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.82% 93.99%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.73% 95.89%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.90% 91.07%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.56% 99.23%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.91% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 82.51% 91.19%
CHEMBL233 P35372 Mu opioid receptor 82.35% 97.93%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.34% 93.56%

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 46880978
NPASS NPC25850
LOTUS LTS0114795
wikiData Q105217019