(Z)-lowdenic acid

Details

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Internal ID a41bac01-d94a-4f80-913a-64f4084f393a
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 2-[(2S,4Z)-4-[(5R)-5-methyl-5-[(4S)-4-methyltetradecyl]furan-2-ylidene]-3,5-dioxooxolan-2-yl]acetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H40O6/c1-4-5-6-7-8-9-10-11-13-19(2)14-12-16-26(3)17-15-20(32-26)23-24(29)21(18-22(27)28)31-25(23)30/h15,17,19,21H,4-14,16,18H2,1-3H3,(H,27,28)/b23-20-/t19-,21-,26+/m0/s1
InChI Key GTHQWTZYJQZCCN-QOZNHZNQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H40O6
Molecular Weight 448.60 g/mol
Exact Mass 448.28248899 g/mol
Topological Polar Surface Area (TPSA) 89.90 Ų
XlogP 7.70
Atomic LogP (AlogP) 5.89
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (Z)-lowdenic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 - 0.6288 62.88%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.7085 70.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8146 81.46%
OATP1B3 inhibitior + 0.8953 89.53%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8986 89.86%
P-glycoprotein inhibitior + 0.6371 63.71%
P-glycoprotein substrate + 0.5140 51.40%
CYP3A4 substrate + 0.5986 59.86%
CYP2C9 substrate - 0.7763 77.63%
CYP2D6 substrate - 0.9064 90.64%
CYP3A4 inhibition - 0.6527 65.27%
CYP2C9 inhibition - 0.8660 86.60%
CYP2C19 inhibition - 0.8171 81.71%
CYP2D6 inhibition - 0.9472 94.72%
CYP1A2 inhibition - 0.8017 80.17%
CYP2C8 inhibition - 0.6671 66.71%
CYP inhibitory promiscuity - 0.9519 95.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5058 50.58%
Eye corrosion - 0.9843 98.43%
Eye irritation - 0.8831 88.31%
Skin irritation + 0.6136 61.36%
Skin corrosion - 0.9131 91.31%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5593 55.93%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5176 51.76%
skin sensitisation - 0.8367 83.67%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.6980 69.80%
Acute Oral Toxicity (c) III 0.4655 46.55%
Estrogen receptor binding + 0.7196 71.96%
Androgen receptor binding + 0.7045 70.45%
Thyroid receptor binding - 0.5978 59.78%
Glucocorticoid receptor binding + 0.7519 75.19%
Aromatase binding + 0.5180 51.80%
PPAR gamma - 0.5133 51.33%
Honey bee toxicity - 0.9633 96.33%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6960 69.60%
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
CHEMBL230 P35354 Cyclooxygenase-2 96.90% 89.63%
CHEMBL2581 P07339 Cathepsin D 96.72% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.18% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.22% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 95.18% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.34% 99.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.89% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.19% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.88% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 84.82% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.44% 99.23%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.42% 89.00%
CHEMBL1907 P15144 Aminopeptidase N 83.38% 93.31%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.18% 100.00%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.95% 97.29%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.74% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.67% 90.71%
CHEMBL299 P17252 Protein kinase C alpha 81.34% 98.03%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.11% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.17% 96.47%

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 139585594
LOTUS LTS0199531
wikiData Q77479626