Tanzawaic acid V

Details

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Internal ID 72aaa346-86fb-44ce-92ff-9e01b7ceb0e0
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Medium-chain fatty acids
IUPAC Name 5-[(1R,2S,4aR,6R,8R,8aS)-1,6-dihydroxy-2,6,8-trimethyl-2,4a,5,7,8,8a-hexahydronaphthalen-1-yl]penta-2,4-dienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H26O4/c1-12-10-17(3,21)11-14-8-7-13(2)18(22,16(12)14)9-5-4-6-15(19)20/h4-9,12-14,16,21-22H,10-11H2,1-3H3,(H,19,20)/t12-,13+,14+,16+,17-,18-/m1/s1
InChI Key WLEJNMDXTCOJFJ-RMWQOVRUSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H26O4
Molecular Weight 306.40 g/mol
Exact Mass 306.18310931 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 2.20
Atomic LogP (AlogP) 2.53
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Tanzawaic acid V

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9852 98.52%
Caco-2 + 0.6180 61.80%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6672 66.72%
OATP2B1 inhibitior - 0.8602 86.02%
OATP1B1 inhibitior + 0.9235 92.35%
OATP1B3 inhibitior + 0.9583 95.83%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5584 55.84%
P-glycoprotein inhibitior - 0.9085 90.85%
P-glycoprotein substrate - 0.7774 77.74%
CYP3A4 substrate + 0.5928 59.28%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.9134 91.34%
CYP3A4 inhibition - 0.7729 77.29%
CYP2C9 inhibition - 0.9438 94.38%
CYP2C19 inhibition - 0.9429 94.29%
CYP2D6 inhibition - 0.9559 95.59%
CYP1A2 inhibition - 0.8584 85.84%
CYP2C8 inhibition - 0.8125 81.25%
CYP inhibitory promiscuity - 0.9430 94.30%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9213 92.13%
Carcinogenicity (trinary) Non-required 0.5739 57.39%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.9797 97.97%
Skin irritation + 0.5562 55.62%
Skin corrosion - 0.9330 93.30%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.6800 68.00%
Hepatotoxicity + 0.5617 56.17%
skin sensitisation - 0.6208 62.08%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5828 58.28%
Acute Oral Toxicity (c) III 0.7682 76.82%
Estrogen receptor binding + 0.8138 81.38%
Androgen receptor binding + 0.5620 56.20%
Thyroid receptor binding - 0.5079 50.79%
Glucocorticoid receptor binding + 0.5483 54.83%
Aromatase binding + 0.5644 56.44%
PPAR gamma + 0.5526 55.26%
Honey bee toxicity - 0.8509 85.09%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9721 97.21%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.84% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.85% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.74% 86.33%
CHEMBL206 P03372 Estrogen receptor alpha 84.05% 97.64%
CHEMBL230 P35354 Cyclooxygenase-2 83.90% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.77% 97.25%
CHEMBL340 P08684 Cytochrome P450 3A4 83.36% 91.19%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.81% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 81.37% 90.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.21% 94.45%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.23% 92.94%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139590566
LOTUS LTS0093780
wikiData Q105307915