1-(4-Methoxy-1,3-dihydro-2-benzofuran-1-yl)hexane-2,3-diol

Details

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Internal ID e5153dde-bda4-4bb2-bad2-495fb5df1746
Taxonomy Organoheterocyclic compounds > Isocoumarans
IUPAC Name 1-(4-methoxy-1,3-dihydro-2-benzofuran-1-yl)hexane-2,3-diol
SMILES (Canonical) CCCC(C(CC1C2=C(CO1)C(=CC=C2)OC)O)O
SMILES (Isomeric) CCCC(C(CC1C2=C(CO1)C(=CC=C2)OC)O)O
InChI InChI=1S/C15H22O4/c1-3-5-12(16)13(17)8-15-10-6-4-7-14(18-2)11(10)9-19-15/h4,6-7,12-13,15-17H,3,5,8-9H2,1-2H3
InChI Key AKISWEDXENVJGK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O4
Molecular Weight 266.33 g/mol
Exact Mass 266.15180918 g/mol
Topological Polar Surface Area (TPSA) 58.90 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.18
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1-(4-Methoxy-1,3-dihydro-2-benzofuran-1-yl)hexane-2,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9806 98.06%
Caco-2 + 0.7271 72.71%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7447 74.47%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9453 94.53%
OATP1B3 inhibitior + 0.9399 93.99%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7042 70.42%
BSEP inhibitior - 0.7208 72.08%
P-glycoprotein inhibitior - 0.9390 93.90%
P-glycoprotein substrate + 0.5266 52.66%
CYP3A4 substrate + 0.5482 54.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4758 47.58%
CYP3A4 inhibition - 0.6156 61.56%
CYP2C9 inhibition - 0.7803 78.03%
CYP2C19 inhibition - 0.5927 59.27%
CYP2D6 inhibition - 0.8621 86.21%
CYP1A2 inhibition + 0.7222 72.22%
CYP2C8 inhibition - 0.5955 59.55%
CYP inhibitory promiscuity - 0.7610 76.10%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Non-required 0.6170 61.70%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.9817 98.17%
Skin irritation - 0.8025 80.25%
Skin corrosion - 0.9520 95.20%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7459 74.59%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.5943 59.43%
skin sensitisation - 0.7517 75.17%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.7727 77.27%
Acute Oral Toxicity (c) III 0.6209 62.09%
Estrogen receptor binding - 0.6080 60.80%
Androgen receptor binding - 0.7146 71.46%
Thyroid receptor binding - 0.5875 58.75%
Glucocorticoid receptor binding - 0.5216 52.16%
Aromatase binding - 0.8538 85.38%
PPAR gamma - 0.6235 62.35%
Honey bee toxicity - 0.8819 88.19%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.8564 85.64%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.76% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.32% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.70% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.18% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.93% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.93% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.87% 93.56%
CHEMBL221 P23219 Cyclooxygenase-1 89.67% 90.17%
CHEMBL1907 P15144 Aminopeptidase N 89.43% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.63% 99.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.04% 93.99%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.97% 97.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.59% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.24% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.50% 85.14%
CHEMBL2535 P11166 Glucose transporter 81.99% 98.75%

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 162996971
LOTUS LTS0014667
wikiData Q103816198