3-Hydroxy-1,5-dioxacyclohenicosane-6,21-dione

Details

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Internal ID 3cb958eb-fdf2-4358-addd-f65e20812c9c
Taxonomy Phenylpropanoids and polyketides > Macrolides and analogues
IUPAC Name 3-hydroxy-1,5-dioxacyclohenicosane-6,21-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H34O5/c20-17-15-23-18(21)13-11-9-7-5-3-1-2-4-6-8-10-12-14-19(22)24-16-17/h17,20H,1-16H2
InChI Key CGRXXYHVIMAIGM-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H34O5
Molecular Weight 342.50 g/mol
Exact Mass 342.24062418 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 5.20
Atomic LogP (AlogP) 3.91
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Hydroxy-1,5-dioxacyclohenicosane-6,21-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8426 84.26%
Caco-2 - 0.6468 64.68%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8460 84.60%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9684 96.84%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6714 67.14%
P-glycoprotein inhibitior - 0.8361 83.61%
P-glycoprotein substrate - 0.9825 98.25%
CYP3A4 substrate - 0.6684 66.84%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8156 81.56%
CYP3A4 inhibition - 0.9636 96.36%
CYP2C9 inhibition - 0.9406 94.06%
CYP2C19 inhibition - 0.9408 94.08%
CYP2D6 inhibition - 0.9561 95.61%
CYP1A2 inhibition - 0.9612 96.12%
CYP2C8 inhibition - 0.9931 99.31%
CYP inhibitory promiscuity - 0.9973 99.73%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6561 65.61%
Eye corrosion - 0.6900 69.00%
Eye irritation + 0.7874 78.74%
Skin irritation - 0.8067 80.67%
Skin corrosion - 0.9455 94.55%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4496 44.96%
Micronuclear - 0.8900 89.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.9580 95.80%
Respiratory toxicity - 0.7889 78.89%
Reproductive toxicity - 0.8000 80.00%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity - 0.6544 65.44%
Acute Oral Toxicity (c) III 0.5622 56.22%
Estrogen receptor binding + 0.5403 54.03%
Androgen receptor binding - 0.9441 94.41%
Thyroid receptor binding - 0.5613 56.13%
Glucocorticoid receptor binding - 0.6940 69.40%
Aromatase binding - 0.6513 65.13%
PPAR gamma - 0.5706 57.06%
Honey bee toxicity - 0.8596 85.96%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.8384 83.84%

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 91.65% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.45% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.55% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.43% 92.62%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.36% 96.77%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.71% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.66% 89.00%

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.
Thapsia garganica

Cross-Links

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PubChem 11772250
LOTUS LTS0207504
wikiData Q104958112