Lantalucratin D

Details

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Internal ID ce54b64f-e7b1-4810-95fa-99782eb0ada8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Vitamin K compounds
IUPAC Name 2-(2-hydroxy-3-methylbut-3-enyl)-3,5-dimethoxynaphthalene-1,4-dione
SMILES (Canonical) CC(=C)C(CC1=C(C(=O)C2=C(C1=O)C=CC=C2OC)OC)O
SMILES (Isomeric) CC(=C)C(CC1=C(C(=O)C2=C(C1=O)C=CC=C2OC)OC)O
InChI InChI=1S/C17H18O5/c1-9(2)12(18)8-11-15(19)10-6-5-7-13(21-3)14(10)16(20)17(11)22-4/h5-7,12,18H,1,8H2,2-4H3
InChI Key QZJGWBYRONMDNW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H18O5
Molecular Weight 302.32 g/mol
Exact Mass 302.11542367 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.30
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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CHEMBL451534

2D Structure

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2D Structure of Lantalucratin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.7495 74.95%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6239 62.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9404 94.04%
OATP1B3 inhibitior + 0.9233 92.33%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5261 52.61%
P-glycoprotein inhibitior - 0.8464 84.64%
P-glycoprotein substrate - 0.7028 70.28%
CYP3A4 substrate + 0.5511 55.11%
CYP2C9 substrate - 0.7936 79.36%
CYP2D6 substrate - 0.7797 77.97%
CYP3A4 inhibition - 0.5490 54.90%
CYP2C9 inhibition - 0.7914 79.14%
CYP2C19 inhibition - 0.5274 52.74%
CYP2D6 inhibition - 0.7883 78.83%
CYP1A2 inhibition + 0.6231 62.31%
CYP2C8 inhibition - 0.7498 74.98%
CYP inhibitory promiscuity - 0.6186 61.86%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9561 95.61%
Carcinogenicity (trinary) Non-required 0.7095 70.95%
Eye corrosion - 0.9880 98.80%
Eye irritation - 0.5688 56.88%
Skin irritation - 0.6906 69.06%
Skin corrosion - 0.9587 95.87%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7197 71.97%
Micronuclear - 0.5482 54.82%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.6390 63.90%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity + 0.7962 79.62%
Acute Oral Toxicity (c) III 0.4926 49.26%
Estrogen receptor binding + 0.7106 71.06%
Androgen receptor binding - 0.5186 51.86%
Thyroid receptor binding + 0.5299 52.99%
Glucocorticoid receptor binding + 0.5596 55.96%
Aromatase binding - 0.4838 48.38%
PPAR gamma + 0.5658 56.58%
Honey bee toxicity - 0.7685 76.85%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6600 66.00%
Fish aquatic toxicity + 0.9887 98.87%

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 98.90% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.12% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.97% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 94.88% 85.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.63% 86.33%
CHEMBL2535 P11166 Glucose transporter 89.51% 98.75%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.36% 96.00%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 85.92% 96.67%
CHEMBL1255126 O15151 Protein Mdm4 84.76% 90.20%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 84.71% 97.21%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.23% 97.14%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.57% 96.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 82.31% 82.69%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.12% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.61% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.64% 99.17%

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.
Lantana involucrata

Cross-Links

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PubChem 11426608
LOTUS LTS0045254
wikiData Q105232104