Morelin

Details

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Internal ID a7f252d9-72ca-4676-a5bf-59d5f885a4b7
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acid esters > Coumaric acid esters
IUPAC Name methyl (E)-3-(2-hydroxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H10O3/c1-13-10(12)7-6-8-4-2-3-5-9(8)11/h2-7,11H,1H3/b7-6+
InChI Key YMXREWKKROWOSO-VOTSOKGWSA-N
Popularity 15 references in papers

Physical and Chemical Properties

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Molecular Formula C10H10O3
Molecular Weight 178.18 g/mol
Exact Mass 178.062994177 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.58
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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methyl (E)-3-(2-hydroxyphenyl)prop-2-enoate
RefChem:1089844
3-(2-Hydroxyphenyl)acrylic acid methyl ester
6236-69-7
2-Propenoic acid, 3-(2-hydroxyphenyl)-, methyl ester
Methyl (2E)-3-(2-hydroxyphenyl)-2-propenoate
2-Propenoic acid, 3-(2-hydroxyphenyl)-, methyl ester, (2E)-
Methyl o-coumarate
METHYL-C-COUMARATE
o-coumaric acid methyl ester
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Morelin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9974 99.74%
Caco-2 + 0.9105 91.05%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.9164 91.64%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9379 93.79%
OATP1B3 inhibitior + 0.9878 98.78%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8674 86.74%
P-glycoprotein inhibitior - 0.9769 97.69%
P-glycoprotein substrate - 0.9578 95.78%
CYP3A4 substrate - 0.5972 59.72%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.8578 85.78%
CYP3A4 inhibition - 0.9412 94.12%
CYP2C9 inhibition - 0.8822 88.22%
CYP2C19 inhibition - 0.7815 78.15%
CYP2D6 inhibition - 0.9692 96.92%
CYP1A2 inhibition - 0.7140 71.40%
CYP2C8 inhibition - 0.7329 73.29%
CYP inhibitory promiscuity - 0.8247 82.47%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.6451 64.51%
Carcinogenicity (trinary) Non-required 0.5956 59.56%
Eye corrosion + 0.7434 74.34%
Eye irritation + 0.9917 99.17%
Skin irritation + 0.8557 85.57%
Skin corrosion - 0.9337 93.37%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7193 71.93%
Micronuclear + 0.5137 51.37%
Hepatotoxicity + 0.5072 50.72%
skin sensitisation - 0.8124 81.24%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.5426 54.26%
Acute Oral Toxicity (c) III 0.7730 77.30%
Estrogen receptor binding - 0.6118 61.18%
Androgen receptor binding - 0.5654 56.54%
Thyroid receptor binding - 0.7917 79.17%
Glucocorticoid receptor binding - 0.4915 49.15%
Aromatase binding + 0.6316 63.16%
PPAR gamma - 0.8209 82.09%
Honey bee toxicity - 0.9525 95.25%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.9580 95.80%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.72% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.53% 95.56%
CHEMBL2581 P07339 Cathepsin D 88.56% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.76% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.67% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 83.70% 94.73%
CHEMBL4208 P20618 Proteasome component C5 80.60% 90.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 80.07% 98.11%

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.
There are no matching plants.

Cross-Links

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PubChem 5370693
LOTUS LTS0090105
wikiData Q105350801