Diplodialide C

Details

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Internal ID f42820b8-1a10-4538-bcc4-f5728b8389d9
Taxonomy Organoheterocyclic compounds > Lactones
IUPAC Name 4-hydroxy-10-methyloxecan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H18O3/c1-8-5-3-2-4-6-9(11)7-10(12)13-8/h8-9,11H,2-7H2,1H3
InChI Key FYKUVQXVABYKIC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C10H18O3
Molecular Weight 186.25 g/mol
Exact Mass 186.125594432 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.63
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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FYKUVQXVABYKIC-UHFFFAOYSA-N
4-Hydroxy-10-methyl-2-oxecanone #
2-Oxecanone, 4-hydroxy-10-methyl-, [4R-(4R*,10R*)]-

2D Structure

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2D Structure of Diplodialide C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9892 98.92%
Caco-2 + 0.8202 82.02%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.6408 64.08%
OATP2B1 inhibitior - 0.8478 84.78%
OATP1B1 inhibitior + 0.9187 91.87%
OATP1B3 inhibitior + 0.9498 94.98%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.9506 95.06%
P-glycoprotein inhibitior - 0.9688 96.88%
P-glycoprotein substrate - 0.9384 93.84%
CYP3A4 substrate - 0.6010 60.10%
CYP2C9 substrate - 0.7974 79.74%
CYP2D6 substrate - 0.8423 84.23%
CYP3A4 inhibition - 0.8955 89.55%
CYP2C9 inhibition - 0.8968 89.68%
CYP2C19 inhibition - 0.8387 83.87%
CYP2D6 inhibition - 0.9662 96.62%
CYP1A2 inhibition - 0.5912 59.12%
CYP2C8 inhibition - 0.9786 97.86%
CYP inhibitory promiscuity - 0.9895 98.95%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.6460 64.60%
Eye corrosion - 0.7503 75.03%
Eye irritation + 0.8995 89.95%
Skin irritation + 0.6583 65.83%
Skin corrosion - 0.6502 65.02%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6925 69.25%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.6969 69.69%
skin sensitisation - 0.7989 79.89%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity - 0.5473 54.73%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.6478 64.78%
Acute Oral Toxicity (c) III 0.6245 62.45%
Estrogen receptor binding - 0.9142 91.42%
Androgen receptor binding - 0.7637 76.37%
Thyroid receptor binding - 0.7240 72.40%
Glucocorticoid receptor binding - 0.7612 76.12%
Aromatase binding - 0.8284 82.84%
PPAR gamma - 0.8568 85.68%
Honey bee toxicity - 0.9756 97.56%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.6911 69.11%

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 91.61% 98.95%
CHEMBL3012 Q13946 Phosphodiesterase 7A 87.95% 99.29%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.79% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.17% 97.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.22% 90.71%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.46% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.42% 99.23%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.92% 97.25%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.88% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.90% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.86% 91.11%
CHEMBL5255 O00206 Toll-like receptor 4 80.18% 92.50%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.16% 92.94%

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 560645
LOTUS LTS0054695
wikiData Q105004549