6-(1,2-Dihydroxy-2-phenylethyl)-4-hydroxyoxan-2-one

Details

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Internal ID d77340aa-bb2e-49ce-aac3-98dba97031e3
Taxonomy Organoheterocyclic compounds > Lactones > Delta valerolactones
IUPAC Name 6-(1,2-dihydroxy-2-phenylethyl)-4-hydroxyoxan-2-one
SMILES (Canonical) C1C(CC(=O)OC1C(C(C2=CC=CC=C2)O)O)O
SMILES (Isomeric) C1C(CC(=O)OC1C(C(C2=CC=CC=C2)O)O)O
InChI InChI=1S/C13H16O5/c14-9-6-10(18-11(15)7-9)13(17)12(16)8-4-2-1-3-5-8/h1-5,9-10,12-14,16-17H,6-7H2
InChI Key XMOGEOVHRGIFNH-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O5
Molecular Weight 252.26 g/mol
Exact Mass 252.09977361 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.15
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-(1,2-Dihydroxy-2-phenylethyl)-4-hydroxyoxan-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 + 0.7005 70.05%
Caco-2 - 0.6514 65.14%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7778 77.78%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9305 93.05%
OATP1B3 inhibitior + 0.9571 95.71%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9120 91.20%
P-glycoprotein inhibitior - 0.9332 93.32%
P-glycoprotein substrate - 0.8626 86.26%
CYP3A4 substrate - 0.5885 58.85%
CYP2C9 substrate - 0.6012 60.12%
CYP2D6 substrate - 0.7840 78.40%
CYP3A4 inhibition - 0.9374 93.74%
CYP2C9 inhibition - 0.9519 95.19%
CYP2C19 inhibition - 0.9358 93.58%
CYP2D6 inhibition - 0.9430 94.30%
CYP1A2 inhibition - 0.9448 94.48%
CYP2C8 inhibition - 0.9404 94.04%
CYP inhibitory promiscuity - 0.9854 98.54%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.6528 65.28%
Eye corrosion - 0.9762 97.62%
Eye irritation - 0.7958 79.58%
Skin irritation - 0.6253 62.53%
Skin corrosion - 0.9081 90.81%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7575 75.75%
Micronuclear + 0.5400 54.00%
Hepatotoxicity + 0.6317 63.17%
skin sensitisation - 0.8634 86.34%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.7198 71.98%
Acute Oral Toxicity (c) III 0.5747 57.47%
Estrogen receptor binding - 0.5757 57.57%
Androgen receptor binding - 0.6396 63.96%
Thyroid receptor binding - 0.7852 78.52%
Glucocorticoid receptor binding - 0.5558 55.58%
Aromatase binding - 0.7286 72.86%
PPAR gamma - 0.5871 58.71%
Honey bee toxicity - 0.8651 86.51%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity - 0.4596 45.96%

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 92.63% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.44% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.30% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.01% 85.14%
CHEMBL221 P23219 Cyclooxygenase-1 88.65% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.54% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 87.11% 94.62%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.66% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.32% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.45% 86.33%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.26% 94.08%

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.
Goniothalamus leiocarpus

Cross-Links

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PubChem 73812409
LOTUS LTS0008619
wikiData Q105331322