Marmelo oxide A

Details

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Internal ID 04846536-f910-48fa-af6b-33a5c89d3b44
Taxonomy Organoheterocyclic compounds > Tetrahydrofurans
IUPAC Name (2R,4R)-4-methyl-2-[(1E)-3-methylbuta-1,3-dienyl]oxolane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H16O/c1-8(2)4-5-10-6-9(3)7-11-10/h4-5,9-10H,1,6-7H2,2-3H3/b5-4+/t9-,10+/m1/s1
InChI Key SULWOTZUSYCRIP-CFUOYWMPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H16O
Molecular Weight 152.23 g/mol
Exact Mass 152.120115130 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 2.90
Atomic LogP (AlogP) 2.54
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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CHEBI:171980
(2R,4R)-4-methyl-2-[(1E)-3-methylbuta-1,3-dienyl]oxolane

2D Structure

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2D Structure of Marmelo oxide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9929 99.29%
Caco-2 + 0.8632 86.32%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4072 40.72%
OATP2B1 inhibitior - 0.8617 86.17%
OATP1B1 inhibitior + 0.9362 93.62%
OATP1B3 inhibitior + 0.9563 95.63%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9396 93.96%
P-glycoprotein inhibitior - 0.9861 98.61%
P-glycoprotein substrate - 0.8570 85.70%
CYP3A4 substrate - 0.5742 57.42%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.7678 76.78%
CYP3A4 inhibition - 0.8630 86.30%
CYP2C9 inhibition - 0.8393 83.93%
CYP2C19 inhibition - 0.6221 62.21%
CYP2D6 inhibition - 0.9209 92.09%
CYP1A2 inhibition - 0.5312 53.12%
CYP2C8 inhibition - 0.8657 86.57%
CYP inhibitory promiscuity - 0.5548 55.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6644 66.44%
Carcinogenicity (trinary) Warning 0.4883 48.83%
Eye corrosion + 0.6232 62.32%
Eye irritation + 0.7911 79.11%
Skin irritation + 0.5362 53.62%
Skin corrosion - 0.9118 91.18%
Ames mutagenesis + 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5609 56.09%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.5594 55.94%
skin sensitisation + 0.6231 62.31%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6254 62.54%
Acute Oral Toxicity (c) III 0.6834 68.34%
Estrogen receptor binding - 0.9201 92.01%
Androgen receptor binding - 0.8204 82.04%
Thyroid receptor binding - 0.7230 72.30%
Glucocorticoid receptor binding - 0.9239 92.39%
Aromatase binding - 0.7438 74.38%
PPAR gamma - 0.8838 88.38%
Honey bee toxicity - 0.7028 70.28%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.8060 80.60%

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
CHEMBL1951 P21397 Monoamine oxidase A 92.85% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.01% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.50% 92.94%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.15% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.60% 100.00%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.11% 97.21%
CHEMBL340 P08684 Cytochrome P450 3A4 80.42% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.38% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.15% 86.33%

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.
Cydonia oblonga
Garcinia cowa
Rumex dentatus

Cross-Links

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PubChem 14379832
NPASS NPC161361
LOTUS LTS0239935
wikiData Q105261085