Vulgaredilone

Details

Top
Internal ID 0c3e4510-c7fe-4410-b9fa-b4f633585969
Taxonomy Organoheterocyclic compounds > Benzopyrans > 2-benzopyrans
IUPAC Name 3-dodecyl-6-(3-methylbutyl)-5,6-dihydro-3H-furo[3,2-g]isochromene-2,8-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H42O4/c1-4-5-6-7-8-9-10-11-12-13-14-23-25-18-21-17-22(16-15-20(2)3)31-28(30)24(21)19-26(25)32-27(23)29/h18-20,22-23H,4-17H2,1-3H3
InChI Key ZBZXQEXMHFZLEI-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C28H42O4
Molecular Weight 442.60 g/mol
Exact Mass 442.30830982 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 9.70
Atomic LogP (AlogP) 7.52
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 14

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Vulgaredilone

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.6150 61.50%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.8220 82.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8672 86.72%
OATP1B3 inhibitior + 0.9468 94.68%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.7966 79.66%
P-glycoprotein inhibitior + 0.7719 77.19%
P-glycoprotein substrate + 0.6509 65.09%
CYP3A4 substrate + 0.5952 59.52%
CYP2C9 substrate + 0.6090 60.90%
CYP2D6 substrate - 0.8665 86.65%
CYP3A4 inhibition - 0.6938 69.38%
CYP2C9 inhibition - 0.6092 60.92%
CYP2C19 inhibition + 0.5133 51.33%
CYP2D6 inhibition - 0.8939 89.39%
CYP1A2 inhibition + 0.5368 53.68%
CYP2C8 inhibition - 0.7455 74.55%
CYP inhibitory promiscuity - 0.7848 78.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6903 69.03%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.6644 66.44%
Skin irritation - 0.7848 78.48%
Skin corrosion - 0.8945 89.45%
Ames mutagenesis - 0.6457 64.57%
Human Ether-a-go-go-Related Gene inhibition + 0.7243 72.43%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5900 59.00%
skin sensitisation - 0.8240 82.40%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.5194 51.94%
Acute Oral Toxicity (c) III 0.5701 57.01%
Estrogen receptor binding + 0.6226 62.26%
Androgen receptor binding + 0.6693 66.93%
Thyroid receptor binding - 0.6437 64.37%
Glucocorticoid receptor binding - 0.4752 47.52%
Aromatase binding - 0.6991 69.91%
PPAR gamma - 0.5719 57.19%
Honey bee toxicity - 0.9160 91.60%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6834 68.34%
Fish aquatic toxicity + 1.0000 100.00%

Targets

Top

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 99.61% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.92% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 96.51% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.64% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.07% 96.09%
CHEMBL1907 P15144 Aminopeptidase N 93.98% 93.31%
CHEMBL3359 P21462 Formyl peptide receptor 1 93.04% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.12% 99.17%
CHEMBL1951 P21397 Monoamine oxidase A 91.26% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.37% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.05% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 87.24% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.41% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.25% 94.80%
CHEMBL217 P14416 Dopamine D2 receptor 83.75% 95.62%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.81% 91.81%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.46% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.38% 99.23%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.52% 92.08%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.39% 96.47%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 81.10% 90.24%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.00% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.91% 97.09%
CHEMBL321 P14780 Matrix metalloproteinase 9 80.74% 92.12%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 139585533
LOTUS LTS0021145
wikiData Q77424652