2-(1,3-Dihydroxypropan-2-yl)-3-hydroxy-2,3-dihydro-1-benzofuran-5-carbaldehyde

Details

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Internal ID 3ead9706-9ddc-4406-bd42-4fcf5c74fb42
Taxonomy Organoheterocyclic compounds > Coumarans
IUPAC Name 2-(1,3-dihydroxypropan-2-yl)-3-hydroxy-2,3-dihydro-1-benzofuran-5-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H14O5/c13-4-7-1-2-10-9(3-7)11(16)12(17-10)8(5-14)6-15/h1-4,8,11-12,14-16H,5-6H2
InChI Key NHGRSQQMNDLOIB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H14O5
Molecular Weight 238.24 g/mol
Exact Mass 238.08412354 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP -0.80
Atomic LogP (AlogP) -0.11
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(1,3-Dihydroxypropan-2-yl)-3-hydroxy-2,3-dihydro-1-benzofuran-5-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9320 93.20%
Caco-2 - 0.7283 72.83%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5473 54.73%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8899 88.99%
OATP1B3 inhibitior + 0.9475 94.75%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9562 95.62%
P-glycoprotein inhibitior - 0.9400 94.00%
P-glycoprotein substrate - 0.9020 90.20%
CYP3A4 substrate - 0.6017 60.17%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6770 67.70%
CYP3A4 inhibition - 0.8776 87.76%
CYP2C9 inhibition - 0.7612 76.12%
CYP2C19 inhibition - 0.7604 76.04%
CYP2D6 inhibition - 0.9377 93.77%
CYP1A2 inhibition - 0.5307 53.07%
CYP2C8 inhibition - 0.8532 85.32%
CYP inhibitory promiscuity + 0.5358 53.58%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6016 60.16%
Eye corrosion - 0.9816 98.16%
Eye irritation - 0.5139 51.39%
Skin irritation - 0.6300 63.00%
Skin corrosion - 0.9348 93.48%
Ames mutagenesis - 0.6078 60.78%
Human Ether-a-go-go-Related Gene inhibition - 0.4942 49.42%
Micronuclear + 0.5240 52.40%
Hepatotoxicity - 0.6007 60.07%
skin sensitisation - 0.6613 66.13%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.5806 58.06%
Acute Oral Toxicity (c) III 0.5164 51.64%
Estrogen receptor binding - 0.4902 49.02%
Androgen receptor binding - 0.5558 55.58%
Thyroid receptor binding - 0.7506 75.06%
Glucocorticoid receptor binding - 0.7533 75.33%
Aromatase binding - 0.7309 73.09%
PPAR gamma + 0.5872 58.72%
Honey bee toxicity - 0.8414 84.14%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.6415 64.15%

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 92.46% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.79% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.91% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.79% 89.00%
CHEMBL2581 P07339 Cathepsin D 87.56% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.99% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.51% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 82.38% 94.80%
CHEMBL3401 O75469 Pregnane X receptor 81.53% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.49% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.36% 94.45%

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 163066252
LOTUS LTS0028358
wikiData Q104172511