Methyl 4,5-dihydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)oxycyclohexene-1-carboxylate

Details

Top
Internal ID 0d9a31bc-2265-4cf1-af4a-23369ce6e040
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Dicarboxylic acids and derivatives
IUPAC Name methyl 4,5-dihydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)oxycyclohexene-1-carboxylate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O7/c1-6(11(15)17-2)19-9-5-7(12(16)18-3)4-8(13)10(9)14/h5,8-10,13-14H,1,4H2,2-3H3
InChI Key LXXNOOUDPRVEFK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C12H16O7
Molecular Weight 272.25 g/mol
Exact Mass 272.08960285 g/mol
Topological Polar Surface Area (TPSA) 102.00 Ų
XlogP -0.10
Atomic LogP (AlogP) -0.72
H-Bond Acceptor 7
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of Methyl 4,5-dihydroxy-3-(3-methoxy-3-oxoprop-1-en-2-yl)oxycyclohexene-1-carboxylate

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9131 91.31%
Caco-2 - 0.7590 75.90%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7908 79.08%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9342 93.42%
OATP1B3 inhibitior + 0.9534 95.34%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9403 94.03%
P-glycoprotein inhibitior - 0.9323 93.23%
P-glycoprotein substrate - 0.7472 74.72%
CYP3A4 substrate + 0.5490 54.90%
CYP2C9 substrate - 0.7965 79.65%
CYP2D6 substrate - 0.8510 85.10%
CYP3A4 inhibition - 0.9000 90.00%
CYP2C9 inhibition - 0.9098 90.98%
CYP2C19 inhibition - 0.8989 89.89%
CYP2D6 inhibition - 0.9174 91.74%
CYP1A2 inhibition - 0.9370 93.70%
CYP2C8 inhibition - 0.8768 87.68%
CYP inhibitory promiscuity - 0.9843 98.43%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8343 83.43%
Carcinogenicity (trinary) Non-required 0.7018 70.18%
Eye corrosion - 0.9601 96.01%
Eye irritation - 0.8985 89.85%
Skin irritation - 0.6907 69.07%
Skin corrosion - 0.9376 93.76%
Ames mutagenesis - 0.6954 69.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7139 71.39%
Micronuclear + 0.5700 57.00%
Hepatotoxicity - 0.5572 55.72%
skin sensitisation - 0.6328 63.28%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.5099 50.99%
Acute Oral Toxicity (c) III 0.4159 41.59%
Estrogen receptor binding - 0.6289 62.89%
Androgen receptor binding - 0.8105 81.05%
Thyroid receptor binding - 0.5991 59.91%
Glucocorticoid receptor binding - 0.5500 55.00%
Aromatase binding - 0.6256 62.56%
PPAR gamma - 0.7269 72.69%
Honey bee toxicity - 0.9029 90.29%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.8939 89.39%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.60% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 96.00% 83.82%
CHEMBL2581 P07339 Cathepsin D 94.32% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.42% 91.11%
CHEMBL4208 P20618 Proteasome component C5 83.66% 90.00%
CHEMBL340 P08684 Cytochrome P450 3A4 82.97% 91.19%
CHEMBL221 P23219 Cyclooxygenase-1 81.02% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.55% 95.89%

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 73201099
LOTUS LTS0160663
wikiData Q104171439