Deacetylmycoepoxydiene

Details

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Internal ID 17a0f01f-4891-4dab-b064-f665e08cff2b
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name (2S,3S)-3-hydroxy-2-[(1R,6S,7R,8S)-8-methyl-9-oxabicyclo[4.2.1]nona-2,4-dien-7-yl]-2,3-dihydropyran-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C14H16O4/c1-8-10-4-2-3-5-11(17-10)13(8)14-9(15)6-7-12(16)18-14/h2-11,13-15H,1H3/t8-,9+,10-,11+,13-,14-/m1/s1
InChI Key RTPJTLADTXRGCF-PNQJMIKCSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C14H16O4
Molecular Weight 248.27 g/mol
Exact Mass 248.10485899 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.40
Atomic LogP (AlogP) 0.97
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Deacetylmycoepoxydiene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9821 98.21%
Caco-2 + 0.6620 66.20%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6446 64.46%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8677 86.77%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9371 93.71%
P-glycoprotein inhibitior - 0.9384 93.84%
P-glycoprotein substrate - 0.9213 92.13%
CYP3A4 substrate - 0.5327 53.27%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9005 90.05%
CYP3A4 inhibition - 0.7355 73.55%
CYP2C9 inhibition - 0.8958 89.58%
CYP2C19 inhibition - 0.7727 77.27%
CYP2D6 inhibition - 0.9392 93.92%
CYP1A2 inhibition - 0.7964 79.64%
CYP2C8 inhibition - 0.9602 96.02%
CYP inhibitory promiscuity - 0.8623 86.23%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4228 42.28%
Eye corrosion - 0.9072 90.72%
Eye irritation - 0.7568 75.68%
Skin irritation + 0.5058 50.58%
Skin corrosion - 0.8808 88.08%
Ames mutagenesis + 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5912 59.12%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.7533 75.33%
skin sensitisation - 0.8349 83.49%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6020 60.20%
Acute Oral Toxicity (c) II 0.3383 33.83%
Estrogen receptor binding - 0.7544 75.44%
Androgen receptor binding - 0.7917 79.17%
Thyroid receptor binding - 0.6897 68.97%
Glucocorticoid receptor binding - 0.5641 56.41%
Aromatase binding - 0.6907 69.07%
PPAR gamma - 0.6724 67.24%
Honey bee toxicity - 0.9153 91.53%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.7006 70.06%

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
CHEMBL4040 P28482 MAP kinase ERK2 93.70% 83.82%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 92.79% 87.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.81% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.85% 95.56%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.16% 81.11%
CHEMBL3401 O75469 Pregnane X receptor 83.50% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.78% 99.23%

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 102416998
LOTUS LTS0187956
wikiData Q77424390