4,8,10-Trihydroxy-12-methyl-1-oxacyclododec-5-en-2-one

Details

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Internal ID 7edd5862-275a-4c8c-a6b8-8f65d2ffe19c
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 4,8,10-trihydroxy-12-methyl-1-oxacyclododec-5-en-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H20O5/c1-8-5-11(15)6-9(13)3-2-4-10(14)7-12(16)17-8/h2,4,8-11,13-15H,3,5-7H2,1H3
InChI Key IYYITHHIGWSWAF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O5
Molecular Weight 244.28 g/mol
Exact Mass 244.13107373 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 0.00
Atomic LogP (AlogP) 0.13
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4,8,10-Trihydroxy-12-methyl-1-oxacyclododec-5-en-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 + 0.9046 90.46%
Caco-2 + 0.5954 59.54%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.5061 50.61%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.8956 89.56%
OATP1B3 inhibitior + 0.9662 96.62%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9230 92.30%
P-glycoprotein inhibitior - 0.9702 97.02%
P-glycoprotein substrate - 0.8967 89.67%
CYP3A4 substrate - 0.5292 52.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8541 85.41%
CYP3A4 inhibition - 0.6721 67.21%
CYP2C9 inhibition - 0.8948 89.48%
CYP2C19 inhibition - 0.8929 89.29%
CYP2D6 inhibition - 0.9511 95.11%
CYP1A2 inhibition - 0.7296 72.96%
CYP2C8 inhibition - 0.9534 95.34%
CYP inhibitory promiscuity - 0.9483 94.83%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8728 87.28%
Carcinogenicity (trinary) Non-required 0.6117 61.17%
Eye corrosion - 0.9355 93.55%
Eye irritation + 0.6468 64.68%
Skin irritation - 0.5596 55.96%
Skin corrosion - 0.7875 78.75%
Ames mutagenesis + 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8274 82.74%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.6627 66.27%
skin sensitisation - 0.7961 79.61%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity + 0.8090 80.90%
Acute Oral Toxicity (c) III 0.5632 56.32%
Estrogen receptor binding - 0.7283 72.83%
Androgen receptor binding - 0.6997 69.97%
Thyroid receptor binding - 0.5908 59.08%
Glucocorticoid receptor binding - 0.4828 48.28%
Aromatase binding - 0.7822 78.22%
PPAR gamma - 0.7097 70.97%
Honey bee toxicity - 0.8724 87.24%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.4123 41.23%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.91% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.12% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.89% 99.23%
CHEMBL2581 P07339 Cathepsin D 82.69% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.54% 89.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.09% 97.09%

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 162856185
LOTUS LTS0091492
wikiData Q104169269