Taiwanin F

Details

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Internal ID ab9dc5ac-741e-4082-a6c0-524e9c3c42c3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (2S,4aS,10aR)-2,5,6-trihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one
SMILES (Canonical) CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(C3(C)C)O)C)O)O
SMILES (Isomeric) CC(C)C1=C(C(=C2C(=C1)C(=O)C[C@@H]3[C@@]2(CC[C@@H](C3(C)C)O)C)O)O
InChI InChI=1S/C20H28O4/c1-10(2)11-8-12-13(21)9-14-19(3,4)15(22)6-7-20(14,5)16(12)18(24)17(11)23/h8,10,14-15,22-24H,6-7,9H2,1-5H3/t14-,15-,20-/m0/s1
InChI Key BJDDFWYEMCOHPH-AVYPCKFXSA-N
Popularity 0 references 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) 77.80 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.86
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Taiwanin F

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9942 99.42%
Caco-2 + 0.5175 51.75%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8753 87.53%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8926 89.26%
OATP1B3 inhibitior + 0.9359 93.59%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8321 83.21%
BSEP inhibitior - 0.6991 69.91%
P-glycoprotein inhibitior - 0.9031 90.31%
P-glycoprotein substrate - 0.7690 76.90%
CYP3A4 substrate + 0.6328 63.28%
CYP2C9 substrate - 0.5905 59.05%
CYP2D6 substrate - 0.7584 75.84%
CYP3A4 inhibition - 0.6897 68.97%
CYP2C9 inhibition - 0.9130 91.30%
CYP2C19 inhibition - 0.8526 85.26%
CYP2D6 inhibition - 0.9566 95.66%
CYP1A2 inhibition + 0.6872 68.72%
CYP2C8 inhibition - 0.7845 78.45%
CYP inhibitory promiscuity - 0.9620 96.20%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6584 65.84%
Eye corrosion - 0.9923 99.23%
Eye irritation - 0.8165 81.65%
Skin irritation + 0.4909 49.09%
Skin corrosion - 0.9292 92.92%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7780 77.80%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5041 50.41%
skin sensitisation - 0.7855 78.55%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.7585 75.85%
Acute Oral Toxicity (c) III 0.7071 70.71%
Estrogen receptor binding + 0.6047 60.47%
Androgen receptor binding - 0.5648 56.48%
Thyroid receptor binding + 0.6643 66.43%
Glucocorticoid receptor binding + 0.8617 86.17%
Aromatase binding + 0.6314 63.14%
PPAR gamma + 0.7035 70.35%
Honey bee toxicity - 0.7644 76.44%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9953 99.53%

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
CHEMBL2581 P07339 Cathepsin D 98.08% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.28% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 94.33% 90.71%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.15% 96.77%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.30% 95.56%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 90.14% 96.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.08% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.05% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.89% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.95% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 88.70% 99.15%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.57% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.38% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.86% 94.45%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 85.92% 85.11%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 85.67% 93.03%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 85.59% 90.24%
CHEMBL1907 P15144 Aminopeptidase N 84.97% 93.31%
CHEMBL340 P08684 Cytochrome P450 3A4 83.04% 91.19%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.34% 93.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.49% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.66% 99.23%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 80.43% 92.88%

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.
Salvia pubescens
Taiwania cryptomerioides
Torreya nucifera

Cross-Links

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PubChem 13970371
NPASS NPC181007
LOTUS LTS0057169
wikiData Q104936983