Lasionectrin

Details

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Internal ID df29af26-0185-4bdd-a2ef-04bf8fe532d5
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones
IUPAC Name (11R,13R,15R)-2,4-dihydroxy-6-methoxy-13-propyl-12,16-dioxatetracyclo[8.7.0.03,8.011,15]heptadeca-1,3,5,7,9-pentaen-17-one
SMILES (Canonical) CCCC1CC2C(O1)C3=CC4=CC(=CC(=C4C(=C3C(=O)O2)O)O)OC
SMILES (Isomeric) CCC[C@@H]1C[C@@H]2[C@H](O1)C3=CC4=CC(=CC(=C4C(=C3C(=O)O2)O)O)OC
InChI InChI=1S/C19H20O6/c1-3-4-10-8-14-18(24-10)12-6-9-5-11(23-2)7-13(20)15(9)17(21)16(12)19(22)25-14/h5-7,10,14,18,20-21H,3-4,8H2,1-2H3/t10-,14-,18-/m1/s1
InChI Key OCUDSIWZMMILTN-MAZCYNQFSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O6
Molecular Weight 344.40 g/mol
Exact Mass 344.12598835 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.43
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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CHEMBL2063170

2D Structure

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2D Structure of Lasionectrin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9088 90.88%
Caco-2 + 0.6505 65.05%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6900 69.00%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8540 85.40%
OATP1B3 inhibitior - 0.2243 22.43%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7940 79.40%
P-glycoprotein inhibitior - 0.5610 56.10%
P-glycoprotein substrate - 0.7026 70.26%
CYP3A4 substrate + 0.6012 60.12%
CYP2C9 substrate + 0.6290 62.90%
CYP2D6 substrate - 0.8305 83.05%
CYP3A4 inhibition - 0.5805 58.05%
CYP2C9 inhibition - 0.6378 63.78%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.6602 66.02%
CYP1A2 inhibition + 0.5479 54.79%
CYP2C8 inhibition + 0.5909 59.09%
CYP inhibitory promiscuity + 0.6160 61.60%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5411 54.11%
Eye corrosion - 0.9861 98.61%
Eye irritation - 0.8540 85.40%
Skin irritation - 0.8067 80.67%
Skin corrosion - 0.9392 93.92%
Ames mutagenesis - 0.5924 59.24%
Human Ether-a-go-go-Related Gene inhibition - 0.4821 48.21%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.5052 50.52%
skin sensitisation - 0.8203 82.03%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity + 0.6807 68.07%
Acute Oral Toxicity (c) III 0.5187 51.87%
Estrogen receptor binding + 0.8786 87.86%
Androgen receptor binding + 0.6916 69.16%
Thyroid receptor binding + 0.5932 59.32%
Glucocorticoid receptor binding + 0.8381 83.81%
Aromatase binding + 0.6638 66.38%
PPAR gamma + 0.7641 76.41%
Honey bee toxicity - 0.8821 88.21%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5368 53.68%
Fish aquatic toxicity + 0.9358 93.58%

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 99.34% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.29% 85.14%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 93.48% 92.68%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.45% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.33% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.96% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.68% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.14% 94.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 90.02% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.11% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.05% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.04% 94.45%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.17% 99.23%
CHEMBL4208 P20618 Proteasome component C5 87.59% 90.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 86.14% 96.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.76% 99.15%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 85.26% 91.71%
CHEMBL3401 O75469 Pregnane X receptor 85.17% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 82.49% 93.99%

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 60155242
LOTUS LTS0074599
wikiData Q77563844