6-Hydroxy-3-(4-hydroxy-4-methylpentyl)-3-methyl-2-benzofuran-1-one

Details

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Internal ID 25ea2399-2622-4df2-83b9-304dcad9bd8f
Taxonomy Organoheterocyclic compounds > Benzofurans > Benzofuranones
IUPAC Name 6-hydroxy-3-(4-hydroxy-4-methylpentyl)-3-methyl-2-benzofuran-1-one
SMILES (Canonical) CC1(C2=C(C=C(C=C2)O)C(=O)O1)CCCC(C)(C)O
SMILES (Isomeric) CC1(C2=C(C=C(C=C2)O)C(=O)O1)CCCC(C)(C)O
InChI InChI=1S/C15H20O4/c1-14(2,18)7-4-8-15(3)12-6-5-10(16)9-11(12)13(17)19-15/h5-6,9,16,18H,4,7-8H2,1-3H3
InChI Key CCQGRYZTOPBJQP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H20O4
Molecular Weight 264.32 g/mol
Exact Mass 264.13615911 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.72
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Hydroxy-3-(4-hydroxy-4-methylpentyl)-3-methyl-2-benzofuran-1-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9903 99.03%
Caco-2 + 0.8128 81.28%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Mitochondria 0.7454 74.54%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior - 0.3337 33.37%
OATP1B3 inhibitior + 0.8979 89.79%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7080 70.80%
P-glycoprotein inhibitior - 0.9664 96.64%
P-glycoprotein substrate - 0.6055 60.55%
CYP3A4 substrate + 0.5922 59.22%
CYP2C9 substrate - 0.6048 60.48%
CYP2D6 substrate - 0.7905 79.05%
CYP3A4 inhibition - 0.7043 70.43%
CYP2C9 inhibition - 0.8341 83.41%
CYP2C19 inhibition - 0.8476 84.76%
CYP2D6 inhibition - 0.9100 91.00%
CYP1A2 inhibition + 0.5811 58.11%
CYP2C8 inhibition + 0.5538 55.38%
CYP inhibitory promiscuity - 0.8208 82.08%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.5910 59.10%
Eye corrosion - 0.9875 98.75%
Eye irritation + 0.5878 58.78%
Skin irritation - 0.6237 62.37%
Skin corrosion - 0.8450 84.50%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5220 52.20%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5823 58.23%
skin sensitisation - 0.7315 73.15%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5333 53.33%
Acute Oral Toxicity (c) III 0.6301 63.01%
Estrogen receptor binding + 0.7158 71.58%
Androgen receptor binding + 0.5571 55.71%
Thyroid receptor binding + 0.6982 69.82%
Glucocorticoid receptor binding + 0.5471 54.71%
Aromatase binding + 0.5773 57.73%
PPAR gamma + 0.6093 60.93%
Honey bee toxicity - 0.8880 88.80%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9449 94.49%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.09% 91.11%
CHEMBL2581 P07339 Cathepsin D 97.65% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.04% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.71% 95.56%
CHEMBL1951 P21397 Monoamine oxidase A 91.43% 91.49%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 91.01% 90.93%
CHEMBL3401 O75469 Pregnane X receptor 90.67% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.83% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.27% 89.00%
CHEMBL4208 P20618 Proteasome component C5 80.48% 90.00%

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 162863497
LOTUS LTS0198812
wikiData Q103817616