(2,3a-dihydroxy-4,4,7a-trimethyl-3-oxo-6,7-dihydro-5H-1-benzofuran-6-yl) acetate

Details

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Internal ID 997d99f6-b2f2-4276-8001-7f56389eca3f
Taxonomy Organoheterocyclic compounds > Benzofurans
IUPAC Name (2,3a-dihydroxy-4,4,7a-trimethyl-3-oxo-6,7-dihydro-5H-1-benzofuran-6-yl) acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H20O6/c1-7(14)18-8-5-11(2,3)13(17)9(15)10(16)19-12(13,4)6-8/h8,10,16-17H,5-6H2,1-4H3
InChI Key UXCJSPHEVUMWLQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H20O6
Molecular Weight 272.29 g/mol
Exact Mass 272.12598835 g/mol
Topological Polar Surface Area (TPSA) 93.10 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.15
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2,3a-dihydroxy-4,4,7a-trimethyl-3-oxo-6,7-dihydro-5H-1-benzofuran-6-yl) acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8539 85.39%
Caco-2 - 0.6691 66.91%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7025 70.25%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.9497 94.97%
OATP1B3 inhibitior + 0.9122 91.22%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9071 90.71%
P-glycoprotein inhibitior - 0.9442 94.42%
P-glycoprotein substrate - 0.8564 85.64%
CYP3A4 substrate + 0.5767 57.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8713 87.13%
CYP3A4 inhibition - 0.8052 80.52%
CYP2C9 inhibition - 0.8525 85.25%
CYP2C19 inhibition - 0.8708 87.08%
CYP2D6 inhibition - 0.9545 95.45%
CYP1A2 inhibition - 0.8362 83.62%
CYP2C8 inhibition - 0.9557 95.57%
CYP inhibitory promiscuity - 0.9225 92.25%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9643 96.43%
Carcinogenicity (trinary) Non-required 0.5668 56.68%
Eye corrosion - 0.9830 98.30%
Eye irritation - 0.8259 82.59%
Skin irritation - 0.7224 72.24%
Skin corrosion - 0.8967 89.67%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7240 72.40%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.5857 58.57%
skin sensitisation - 0.8226 82.26%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity + 0.6978 69.78%
Acute Oral Toxicity (c) III 0.3998 39.98%
Estrogen receptor binding + 0.6682 66.82%
Androgen receptor binding + 0.6608 66.08%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6800 68.00%
Aromatase binding - 0.5533 55.33%
PPAR gamma - 0.6700 67.00%
Honey bee toxicity - 0.7506 75.06%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6950 69.50%
Fish aquatic toxicity + 0.9073 90.73%

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 95.06% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.49% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.23% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 87.57% 91.19%
CHEMBL2581 P07339 Cathepsin D 84.35% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.55% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.52% 95.56%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.21% 96.77%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.19% 97.25%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.13% 100.00%

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.
Hedlundia hybrida

Cross-Links

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PubChem 73837163
LOTUS LTS0183269
wikiData Q105280709