(3Z,6S,7R)-3-butylidene-6-hydroxy-7-methoxy-4,5,6,7-tetrahydro-2-benzofuran-1-one

Details

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Internal ID 8502f6fa-c48c-45c4-9d1f-7e444778bbeb
Taxonomy Organoheterocyclic compounds > Isobenzofurans
IUPAC Name (3Z,6S,7R)-3-butylidene-6-hydroxy-7-methoxy-4,5,6,7-tetrahydro-2-benzofuran-1-one
SMILES (Canonical) CCCC=C1C2=C(C(C(CC2)O)OC)C(=O)O1
SMILES (Isomeric) CCC/C=C\1/C2=C([C@H]([C@H](CC2)O)OC)C(=O)O1
InChI InChI=1S/C13H18O4/c1-3-4-5-10-8-6-7-9(14)12(16-2)11(8)13(15)17-10/h5,9,12,14H,3-4,6-7H2,1-2H3/b10-5-/t9-,12-/m0/s1
InChI Key XJEUNELMMQEXLN-WSDNMOEQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H18O4
Molecular Weight 238.28 g/mol
Exact Mass 238.12050905 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.69
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3Z,6S,7R)-3-butylidene-6-hydroxy-7-methoxy-4,5,6,7-tetrahydro-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 + 0.9937 99.37%
Caco-2 + 0.6039 60.39%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6271 62.71%
OATP2B1 inhibitior - 0.8507 85.07%
OATP1B1 inhibitior + 0.9321 93.21%
OATP1B3 inhibitior + 0.9359 93.59%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.7448 74.48%
P-glycoprotein inhibitior - 0.8761 87.61%
P-glycoprotein substrate - 0.8554 85.54%
CYP3A4 substrate + 0.5381 53.81%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8595 85.95%
CYP3A4 inhibition - 0.6883 68.83%
CYP2C9 inhibition - 0.8676 86.76%
CYP2C19 inhibition - 0.7754 77.54%
CYP2D6 inhibition - 0.9078 90.78%
CYP1A2 inhibition - 0.7233 72.33%
CYP2C8 inhibition - 0.8628 86.28%
CYP inhibitory promiscuity - 0.7735 77.35%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5771 57.71%
Eye corrosion - 0.9782 97.82%
Eye irritation - 0.8148 81.48%
Skin irritation - 0.6402 64.02%
Skin corrosion - 0.9344 93.44%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6934 69.34%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.5592 55.92%
skin sensitisation - 0.7864 78.64%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity + 0.4541 45.41%
Acute Oral Toxicity (c) III 0.3396 33.96%
Estrogen receptor binding - 0.6177 61.77%
Androgen receptor binding - 0.5567 55.67%
Thyroid receptor binding - 0.6225 62.25%
Glucocorticoid receptor binding - 0.5420 54.20%
Aromatase binding - 0.9313 93.13%
PPAR gamma + 0.5360 53.60%
Honey bee toxicity - 0.8873 88.73%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.8779 87.79%

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 96.58% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.80% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.63% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.43% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.92% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.87% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.75% 92.62%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.34% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.95% 95.89%

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.
Angelica sinensis

Cross-Links

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PubChem 163025235
LOTUS LTS0258949
wikiData Q105328906