(2R,3R,5Z)-3-hydroxy-2-propyl-3,7,8,9-tetrahydro-2H-oxecine-4,10-dione

Details

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Internal ID e0002beb-e299-4119-bfa7-5743ecb02bf2
Taxonomy Organoheterocyclic compounds > Oxocins
IUPAC Name (2R,3R,5Z)-3-hydroxy-2-propyl-3,7,8,9-tetrahydro-2H-oxecine-4,10-dione
SMILES (Canonical) CCCC1C(C(=O)C=CCCCC(=O)O1)O
SMILES (Isomeric) CCC[C@@H]1[C@H](C(=O)/C=C\CCCC(=O)O1)O
InChI InChI=1S/C12H18O4/c1-2-6-10-12(15)9(13)7-4-3-5-8-11(14)16-10/h4,7,10,12,15H,2-3,5-6,8H2,1H3/b7-4-/t10-,12+/m1/s1
InChI Key LGMKFKSSLVELLO-BABHQGDISA-N
Popularity 1 reference 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) 63.60 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.37
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2R,3R,5Z)-3-hydroxy-2-propyl-3,7,8,9-tetrahydro-2H-oxecine-4,10-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9170 91.70%
Caco-2 + 0.5776 57.76%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6409 64.09%
OATP2B1 inhibitior - 0.8538 85.38%
OATP1B1 inhibitior + 0.8920 89.20%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9044 90.44%
P-glycoprotein inhibitior - 0.9551 95.51%
P-glycoprotein substrate - 0.9206 92.06%
CYP3A4 substrate - 0.5644 56.44%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8929 89.29%
CYP3A4 inhibition - 0.8480 84.80%
CYP2C9 inhibition - 0.9237 92.37%
CYP2C19 inhibition - 0.8627 86.27%
CYP2D6 inhibition - 0.9452 94.52%
CYP1A2 inhibition - 0.8253 82.53%
CYP2C8 inhibition - 0.9583 95.83%
CYP inhibitory promiscuity - 0.9754 97.54%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8843 88.43%
Carcinogenicity (trinary) Non-required 0.6309 63.09%
Eye corrosion - 0.9241 92.41%
Eye irritation + 0.5598 55.98%
Skin irritation + 0.4912 49.12%
Skin corrosion - 0.8020 80.20%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8245 82.45%
Micronuclear - 0.8100 81.00%
Hepatotoxicity - 0.5302 53.02%
skin sensitisation - 0.8163 81.63%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7102 71.02%
Acute Oral Toxicity (c) III 0.5387 53.87%
Estrogen receptor binding - 0.7041 70.41%
Androgen receptor binding - 0.8293 82.93%
Thyroid receptor binding - 0.7934 79.34%
Glucocorticoid receptor binding - 0.5550 55.50%
Aromatase binding - 0.9033 90.33%
PPAR gamma - 0.7705 77.05%
Honey bee toxicity - 0.9620 96.20%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.5832 58.32%
Fish aquatic toxicity + 0.8520 85.20%

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 95.00% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.30% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.63% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.96% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.12% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.74% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 81.94% 94.73%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.10% 100.00%

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 101432512
LOTUS LTS0012228
wikiData Q104401527