(+)-Epoxysuberosin

Details

Top
Internal ID f135557a-6c7a-4224-9940-ae9cfe0141ea
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives
IUPAC Name 6-[[(2R)-3,3-dimethyloxiran-2-yl]methyl]-7-methoxychromen-2-one
SMILES (Canonical) CC1(C(O1)CC2=C(C=C3C(=C2)C=CC(=O)O3)OC)C
SMILES (Isomeric) CC1([C@H](O1)CC2=C(C=C3C(=C2)C=CC(=O)O3)OC)C
InChI InChI=1S/C15H16O4/c1-15(2)13(19-15)7-10-6-9-4-5-14(16)18-12(9)8-11(10)17-3/h4-6,8,13H,7H2,1-3H3/t13-/m1/s1
InChI Key JZRVCRZHZQXYDH-CYBMUJFWSA-N
Popularity 3 references in papers

Physical and Chemical Properties

Top
Molecular Formula C15H16O4
Molecular Weight 260.28 g/mol
Exact Mass 260.10485899 g/mol
Topological Polar Surface Area (TPSA) 48.10 Ų
XlogP 2.50
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

Top
(+)-Epoxysuberosin
6-[[(2R)-3,3-Dimethyloxiran-2-yl]methyl]-7-methoxychromen-2-one
6-[[(2R)-3,3-dimethyl-2-oxiranyl]methyl]-7-methoxy-2H-1-benzopyran-2-one
Epoxysuberosin, (+)-

2D Structure

Top
2D Structure of (+)-Epoxysuberosin

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9835 98.35%
Caco-2 + 0.8757 87.57%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.6316 63.16%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9099 90.99%
OATP1B3 inhibitior + 0.9583 95.83%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5203 52.03%
P-glycoprotein inhibitior - 0.8524 85.24%
P-glycoprotein substrate - 0.6862 68.62%
CYP3A4 substrate - 0.5078 50.78%
CYP2C9 substrate - 0.6506 65.06%
CYP2D6 substrate - 0.8114 81.14%
CYP3A4 inhibition - 0.7397 73.97%
CYP2C9 inhibition - 0.7565 75.65%
CYP2C19 inhibition - 0.5619 56.19%
CYP2D6 inhibition - 0.8760 87.60%
CYP1A2 inhibition - 0.5994 59.94%
CYP2C8 inhibition - 0.5947 59.47%
CYP inhibitory promiscuity - 0.6813 68.13%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9613 96.13%
Carcinogenicity (trinary) Non-required 0.5782 57.82%
Eye corrosion - 0.9818 98.18%
Eye irritation - 0.7298 72.98%
Skin irritation - 0.7807 78.07%
Skin corrosion - 0.9619 96.19%
Ames mutagenesis - 0.7037 70.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6468 64.68%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation - 0.7934 79.34%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5950 59.50%
Estrogen receptor binding + 0.8498 84.98%
Androgen receptor binding + 0.5840 58.40%
Thyroid receptor binding - 0.5696 56.96%
Glucocorticoid receptor binding + 0.6304 63.04%
Aromatase binding + 0.7113 71.13%
PPAR gamma + 0.7950 79.50%
Honey bee toxicity - 0.8207 82.07%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9621 96.21%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.94% 91.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.23% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.37% 96.09%
CHEMBL4306 P22460 Voltage-gated potassium channel subunit Kv1.5 90.46% 94.03%
CHEMBL2581 P07339 Cathepsin D 88.96% 98.95%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.39% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.72% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.37% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.37% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.96% 96.00%
CHEMBL1937 Q92769 Histone deacetylase 2 82.56% 94.75%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.00% 99.17%

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.
Coleonema album
Harbouria trachypleura
Leionema phylicifolium
Lysimachia arvensis
Uncaria perrottetii

Cross-Links

Top
PubChem 11184527
NPASS NPC76676
LOTUS LTS0249517
wikiData Q105137542