5,8-Dihydroxy-12-methyl-1-oxacyclododeca-3,6-dien-2-one

Details

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Internal ID 2967c3ae-b5c9-47c2-af03-b5c87d2cf753
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 5,8-dihydroxy-12-methyl-1-oxacyclododeca-3,6-dien-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H18O4/c1-9-3-2-4-10(13)5-6-11(14)7-8-12(15)16-9/h5-11,13-14H,2-4H2,1H3
InChI Key HUZUQWCSNJQLCI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H18O4
Molecular Weight 226.27 g/mol
Exact Mass 226.12050905 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.00
Atomic LogP (AlogP) 0.94
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5,8-Dihydroxy-12-methyl-1-oxacyclododeca-3,6-dien-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9676 96.76%
Caco-2 + 0.5808 58.08%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6561 65.61%
OATP2B1 inhibitior - 0.8606 86.06%
OATP1B1 inhibitior + 0.8970 89.70%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8321 83.21%
BSEP inhibitior - 0.9585 95.85%
P-glycoprotein inhibitior - 0.9807 98.07%
P-glycoprotein substrate - 0.9261 92.61%
CYP3A4 substrate - 0.5569 55.69%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8873 88.73%
CYP3A4 inhibition - 0.8234 82.34%
CYP2C9 inhibition - 0.9397 93.97%
CYP2C19 inhibition - 0.8995 89.95%
CYP2D6 inhibition - 0.9508 95.08%
CYP1A2 inhibition - 0.5263 52.63%
CYP2C8 inhibition - 0.9884 98.84%
CYP inhibitory promiscuity - 0.9721 97.21%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9128 91.28%
Carcinogenicity (trinary) Non-required 0.6168 61.68%
Eye corrosion - 0.8929 89.29%
Eye irritation - 0.9462 94.62%
Skin irritation + 0.5701 57.01%
Skin corrosion - 0.5736 57.36%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7820 78.20%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5158 51.58%
skin sensitisation - 0.7508 75.08%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6059 60.59%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.5970 59.70%
Acute Oral Toxicity (c) III 0.6516 65.16%
Estrogen receptor binding - 0.6946 69.46%
Androgen receptor binding - 0.8461 84.61%
Thyroid receptor binding - 0.7045 70.45%
Glucocorticoid receptor binding + 0.6817 68.17%
Aromatase binding - 0.7452 74.52%
PPAR gamma - 0.7185 71.85%
Honey bee toxicity - 0.9432 94.32%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity - 0.3839 38.39%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.91% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.94% 98.95%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 88.05% 86.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 86.34% 87.67%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.07% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.70% 97.09%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 84.81% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.62% 99.23%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.52% 95.89%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.11% 90.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.94% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.51% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.45% 96.09%

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 73028120
LOTUS LTS0034022
wikiData Q104168425