Miaolienone

Details

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Internal ID e5a55ec2-f216-4883-b7d1-90fd820bedb9
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 3-(hydroxymethyl)-6-(2-hydroxytetradecan-2-yl)-4-methoxypyran-2-one
SMILES (Canonical) CCCCCCCCCCCCC(C)(C1=CC(=C(C(=O)O1)CO)OC)O
SMILES (Isomeric) CCCCCCCCCCCCC(C)(C1=CC(=C(C(=O)O1)CO)OC)O
InChI InChI=1S/C21H36O5/c1-4-5-6-7-8-9-10-11-12-13-14-21(2,24)19-15-18(25-3)17(16-22)20(23)26-19/h15,22,24H,4-14,16H2,1-3H3
InChI Key YOEVWRYJHFPBMU-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H36O5
Molecular Weight 368.50 g/mol
Exact Mass 368.25627424 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.66
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Miaolienone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9346 93.46%
Caco-2 + 0.6506 65.06%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8613 86.13%
OATP2B1 inhibitior - 0.8532 85.32%
OATP1B1 inhibitior + 0.8510 85.10%
OATP1B3 inhibitior + 0.8593 85.93%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.6292 62.92%
BSEP inhibitior + 0.5645 56.45%
P-glycoprotein inhibitior - 0.5864 58.64%
P-glycoprotein substrate - 0.6480 64.80%
CYP3A4 substrate + 0.5122 51.22%
CYP2C9 substrate - 0.6203 62.03%
CYP2D6 substrate - 0.8372 83.72%
CYP3A4 inhibition + 0.5701 57.01%
CYP2C9 inhibition - 0.7986 79.86%
CYP2C19 inhibition - 0.7927 79.27%
CYP2D6 inhibition - 0.9440 94.40%
CYP1A2 inhibition - 0.5717 57.17%
CYP2C8 inhibition + 0.4635 46.35%
CYP inhibitory promiscuity - 0.9182 91.82%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.7028 70.28%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.7522 75.22%
Skin irritation - 0.7683 76.83%
Skin corrosion - 0.9700 97.00%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7220 72.20%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6426 64.26%
skin sensitisation - 0.8609 86.09%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6648 66.48%
Acute Oral Toxicity (c) III 0.4787 47.87%
Estrogen receptor binding + 0.5949 59.49%
Androgen receptor binding + 0.5967 59.67%
Thyroid receptor binding - 0.5073 50.73%
Glucocorticoid receptor binding + 0.6803 68.03%
Aromatase binding + 0.5621 56.21%
PPAR gamma + 0.8031 80.31%
Honey bee toxicity - 0.9548 95.48%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.6853 68.53%
Fish aquatic toxicity + 0.8994 89.94%

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 97.48% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.25% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 94.86% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.09% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.07% 86.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.90% 92.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.83% 95.56%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.43% 93.99%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.21% 96.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.69% 89.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.33% 100.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.15% 94.00%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.34% 97.14%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.84% 97.29%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.38% 91.81%
CHEMBL1977 P11473 Vitamin D receptor 80.23% 99.43%

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 71600063
LOTUS LTS0029055
wikiData Q77509261