11-O-methyldiplosporin

Details

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Internal ID aefc0314-bb5e-406b-a4a5-3467c3dbf9c1
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name (5S,6R)-6-ethyl-5-hydroxy-3-(methoxymethyl)-5,6,7,8-tetrahydrochromen-4-one
SMILES (Canonical) CCC1CCC2=C(C1O)C(=O)C(=CO2)COC
SMILES (Isomeric) CC[C@@H]1CCC2=C([C@H]1O)C(=O)C(=CO2)COC
InChI InChI=1S/C13H18O4/c1-3-8-4-5-10-11(12(8)14)13(15)9(6-16-2)7-17-10/h7-8,12,14H,3-6H2,1-2H3/t8-,12+/m1/s1
InChI Key WQNHLSNFCSLZQY-PELKAZGASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O4
Molecular Weight 238.28 g/mol
Exact Mass 238.12050905 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 11-O-methyldiplosporin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.8696 86.96%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7580 75.80%
OATP2B1 inhibitior - 0.8499 84.99%
OATP1B1 inhibitior + 0.9305 93.05%
OATP1B3 inhibitior + 0.9364 93.64%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.5810 58.10%
P-glycoprotein inhibitior - 0.9273 92.73%
P-glycoprotein substrate - 0.8631 86.31%
CYP3A4 substrate + 0.5441 54.41%
CYP2C9 substrate - 0.7872 78.72%
CYP2D6 substrate - 0.7959 79.59%
CYP3A4 inhibition - 0.5154 51.54%
CYP2C9 inhibition - 0.6017 60.17%
CYP2C19 inhibition + 0.6391 63.91%
CYP2D6 inhibition - 0.8286 82.86%
CYP1A2 inhibition + 0.7796 77.96%
CYP2C8 inhibition - 0.7587 75.87%
CYP inhibitory promiscuity - 0.6160 61.60%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.7077 70.77%
Eye corrosion - 0.9889 98.89%
Eye irritation - 0.8946 89.46%
Skin irritation - 0.7870 78.70%
Skin corrosion - 0.9557 95.57%
Ames mutagenesis + 0.5046 50.46%
Human Ether-a-go-go-Related Gene inhibition - 0.4665 46.65%
Micronuclear - 0.8700 87.00%
Hepatotoxicity + 0.5617 56.17%
skin sensitisation - 0.8449 84.49%
Respiratory toxicity + 0.7111 71.11%
Reproductive toxicity + 0.8000 80.00%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6718 67.18%
Acute Oral Toxicity (c) III 0.6143 61.43%
Estrogen receptor binding + 0.5412 54.12%
Androgen receptor binding + 0.6115 61.15%
Thyroid receptor binding - 0.5703 57.03%
Glucocorticoid receptor binding + 0.5930 59.30%
Aromatase binding - 0.8059 80.59%
PPAR gamma + 0.6902 69.02%
Honey bee toxicity - 0.8703 87.03%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9392 93.92%

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 95.10% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.00% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.62% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.10% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.95% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.95% 95.56%
CHEMBL226 P30542 Adenosine A1 receptor 85.64% 95.93%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.21% 99.17%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.94% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.37% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.10% 89.00%

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 102236782
LOTUS LTS0005904
wikiData Q75059500