Uvidin-A lactarinate

Details

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Internal ID 49dc5ad1-84c9-4bc0-83c1-eb893c62f799
Taxonomy Organoheterocyclic compounds > Oxepanes
IUPAC Name [(1aR,6aR,7S,7aR)-3,3,6a,7a-tetramethyl-2-oxo-1a,2a,4,5,6,7-hexahydronaphtho[2,3-b]oxiren-7-yl]methyl 6-oxononadecanoate
SMILES (Canonical) CCCCCCCCCCCCCC(=O)CCCCC(=O)OCC1C2(CCCC(C2C(=O)C3C1(O3)C)(C)C)C
SMILES (Isomeric) CCCCCCCCCCCCCC(=O)CCCCC(=O)OC[C@@H]1[C@]2(CCCC(C2C(=O)[C@H]3[C@@]1(O3)C)(C)C)C
InChI InChI=1S/C34H58O5/c1-6-7-8-9-10-11-12-13-14-15-16-20-26(35)21-17-18-22-28(36)38-25-27-33(4)24-19-23-32(2,3)30(33)29(37)31-34(27,5)39-31/h27,30-31H,6-25H2,1-5H3/t27-,30?,31+,33-,34-/m1/s1
InChI Key PMJARFDKONVPPF-NJHRAZRNSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C34H58O5
Molecular Weight 546.80 g/mol
Exact Mass 546.42842495 g/mol
Topological Polar Surface Area (TPSA) 73.00 Ų
XlogP 9.70
Atomic LogP (AlogP) 8.55
H-Bond Acceptor 5
H-Bond Donor 0
Rotatable Bonds 19

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Uvidin-A lactarinate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9840 98.40%
Caco-2 - 0.7219 72.19%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.7206 72.06%
OATP2B1 inhibitior - 0.5704 57.04%
OATP1B1 inhibitior + 0.8064 80.64%
OATP1B3 inhibitior + 0.9687 96.87%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9701 97.01%
P-glycoprotein inhibitior + 0.6985 69.85%
P-glycoprotein substrate - 0.6705 67.05%
CYP3A4 substrate + 0.6402 64.02%
CYP2C9 substrate - 0.6108 61.08%
CYP2D6 substrate - 0.8494 84.94%
CYP3A4 inhibition - 0.8020 80.20%
CYP2C9 inhibition - 0.6736 67.36%
CYP2C19 inhibition - 0.6833 68.33%
CYP2D6 inhibition - 0.9480 94.80%
CYP1A2 inhibition - 0.7780 77.80%
CYP2C8 inhibition + 0.4796 47.96%
CYP inhibitory promiscuity - 0.8912 89.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6540 65.40%
Eye corrosion - 0.9822 98.22%
Eye irritation - 0.8304 83.04%
Skin irritation - 0.7568 75.68%
Skin corrosion - 0.9500 95.00%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4562 45.62%
Micronuclear - 0.5800 58.00%
Hepatotoxicity - 0.6249 62.49%
skin sensitisation - 0.8169 81.69%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.5662 56.62%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7102 71.02%
Acute Oral Toxicity (c) III 0.5175 51.75%
Estrogen receptor binding + 0.6566 65.66%
Androgen receptor binding + 0.5916 59.16%
Thyroid receptor binding - 0.6030 60.30%
Glucocorticoid receptor binding + 0.5404 54.04%
Aromatase binding + 0.5275 52.75%
PPAR gamma - 0.5182 51.82%
Honey bee toxicity - 0.9285 92.85%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.8138 81.38%
Fish aquatic toxicity + 0.9903 99.03%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.65% 91.11%
CHEMBL230 P35354 Cyclooxygenase-2 98.59% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.64% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.30% 96.09%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 93.26% 95.17%
CHEMBL2581 P07339 Cathepsin D 93.10% 98.95%
CHEMBL5255 O00206 Toll-like receptor 4 92.54% 92.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.66% 99.17%
CHEMBL299 P17252 Protein kinase C alpha 91.39% 98.03%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.86% 97.09%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 89.80% 100.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 89.40% 91.81%
CHEMBL2996 Q05655 Protein kinase C delta 87.22% 97.79%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.57% 82.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.56% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.39% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.23% 99.23%
CHEMBL4227 P25090 Lipoxin A4 receptor 85.54% 100.00%
CHEMBL1871 P10275 Androgen Receptor 85.30% 96.43%
CHEMBL325 Q13547 Histone deacetylase 1 84.74% 95.92%
CHEMBL221 P23219 Cyclooxygenase-1 84.70% 90.17%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 84.53% 95.50%
CHEMBL218 P21554 Cannabinoid CB1 receptor 84.37% 96.61%
CHEMBL3401 O75469 Pregnane X receptor 83.32% 94.73%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.39% 92.62%
CHEMBL340 P08684 Cytochrome P450 3A4 81.07% 91.19%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.77% 95.89%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.36% 97.50%
CHEMBL1951 P21397 Monoamine oxidase A 80.01% 91.49%

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 139583767
LOTUS LTS0056804
wikiData Q75067253