Tricycloalternarene K

Details

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Internal ID 12e076d4-8dfe-402e-b234-85d74aa0a333
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 6-[(3aR,5S,9aS)-5-hydroxy-3a-methyl-8-oxo-3,5,6,7,9,9a-hexahydrocyclopenta[b]chromen-1-yl]-2-methylheptanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H30O5/c1-12(5-4-6-13(2)20(24)25)14-9-10-21(3)16(14)11-15-17(22)7-8-18(23)19(15)26-21/h9,12-13,16,18,23H,4-8,10-11H2,1-3H3,(H,24,25)/t12?,13?,16-,18-,21+/m0/s1
InChI Key FYUWZRMRONFOPG-WXVNMQLWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H30O5
Molecular Weight 362.50 g/mol
Exact Mass 362.20932405 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 2.40
Atomic LogP (AlogP) 3.62
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tricycloalternarene K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9756 97.56%
Caco-2 + 0.6598 65.98%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7629 76.29%
OATP2B1 inhibitior - 0.8623 86.23%
OATP1B1 inhibitior + 0.8941 89.41%
OATP1B3 inhibitior + 0.8999 89.99%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6053 60.53%
BSEP inhibitior + 0.6432 64.32%
P-glycoprotein inhibitior - 0.7295 72.95%
P-glycoprotein substrate - 0.5978 59.78%
CYP3A4 substrate + 0.5844 58.44%
CYP2C9 substrate + 0.5973 59.73%
CYP2D6 substrate - 0.8936 89.36%
CYP3A4 inhibition - 0.7411 74.11%
CYP2C9 inhibition - 0.9140 91.40%
CYP2C19 inhibition - 0.8839 88.39%
CYP2D6 inhibition - 0.9503 95.03%
CYP1A2 inhibition - 0.8301 83.01%
CYP2C8 inhibition - 0.8209 82.09%
CYP inhibitory promiscuity - 0.9540 95.40%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6047 60.47%
Eye corrosion - 0.9917 99.17%
Eye irritation - 0.9290 92.90%
Skin irritation + 0.6621 66.21%
Skin corrosion - 0.9274 92.74%
Ames mutagenesis - 0.6744 67.44%
Human Ether-a-go-go-Related Gene inhibition - 0.5790 57.90%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8574 85.74%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity - 0.8370 83.70%
Acute Oral Toxicity (c) I 0.3463 34.63%
Estrogen receptor binding + 0.7030 70.30%
Androgen receptor binding - 0.5296 52.96%
Thyroid receptor binding + 0.5627 56.27%
Glucocorticoid receptor binding + 0.8881 88.81%
Aromatase binding - 0.5461 54.61%
PPAR gamma + 0.5808 58.08%
Honey bee toxicity - 0.9039 90.39%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9714 97.14%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.99% 83.82%
CHEMBL2581 P07339 Cathepsin D 99.07% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.82% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.69% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.81% 93.56%
CHEMBL221 P23219 Cyclooxygenase-1 89.31% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.02% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 87.85% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.41% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.93% 94.45%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 84.22% 96.38%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.08% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.81% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.74% 95.89%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.93% 93.04%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.36% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.03% 99.23%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.53% 96.47%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.51% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 80.25% 92.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 80.07% 95.89%

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.
There are no matching plants.

Cross-Links

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PubChem 146683952
LOTUS LTS0199646
wikiData Q105004745