Methyl vanillate

Details

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Internal ID 4b21920a-b6cb-49d9-bb06-fc9cd1b7ee87
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > M-methoxybenzoic acids and derivatives
IUPAC Name methyl 4-hydroxy-3-methoxybenzoate
SMILES (Canonical) COC1=C(C=CC(=C1)C(=O)OC)O
SMILES (Isomeric) COC1=C(C=CC(=C1)C(=O)OC)O
InChI InChI=1S/C9H10O4/c1-12-8-5-6(9(11)13-2)3-4-7(8)10/h3-5,10H,1-2H3
InChI Key BVWTXUYLKBHMOX-UHFFFAOYSA-N
Popularity 170 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10O4
Molecular Weight 182.17 g/mol
Exact Mass 182.05790880 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 1.80
Atomic LogP (AlogP) 1.19
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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Methyl 4-hydroxy-3-methoxybenzoate
3943-74-6
Methyl 3-methoxy-4-hydroxybenzoate
Vanillic acid, methyl ester
4-Hydroxy-3-methoxybenzoic acid methyl ester
BENZOIC ACID, 4-HYDROXY-3-METHOXY-, METHYL ESTER
Methylvanillate
Vanillic acid methyl ester
MFCD00008438
EINECS 223-525-9
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Methyl vanillate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9829 98.29%
Caco-2 + 0.8818 88.18%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.9093 90.93%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9484 94.84%
OATP1B3 inhibitior + 0.9724 97.24%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9566 95.66%
P-glycoprotein inhibitior - 0.9672 96.72%
P-glycoprotein substrate - 0.9576 95.76%
CYP3A4 substrate - 0.6525 65.25%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7812 78.12%
CYP3A4 inhibition - 0.9430 94.30%
CYP2C9 inhibition - 0.9602 96.02%
CYP2C19 inhibition - 0.9025 90.25%
CYP2D6 inhibition - 0.9537 95.37%
CYP1A2 inhibition - 0.9045 90.45%
CYP2C8 inhibition + 0.6488 64.88%
CYP inhibitory promiscuity - 0.9062 90.62%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7026 70.26%
Carcinogenicity (trinary) Non-required 0.6745 67.45%
Eye corrosion + 0.7114 71.14%
Eye irritation + 0.9876 98.76%
Skin irritation + 0.7548 75.48%
Skin corrosion - 0.9517 95.17%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6118 61.18%
Micronuclear - 0.5093 50.93%
Hepatotoxicity - 0.5251 52.51%
skin sensitisation - 0.8904 89.04%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity - 0.5811 58.11%
Acute Oral Toxicity (c) III 0.5484 54.84%
Estrogen receptor binding + 0.5302 53.02%
Androgen receptor binding - 0.8029 80.29%
Thyroid receptor binding - 0.8205 82.05%
Glucocorticoid receptor binding - 0.7776 77.76%
Aromatase binding - 0.7050 70.50%
PPAR gamma - 0.8029 80.29%
Honey bee toxicity - 0.9796 97.96%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.7766 77.66%
Fish aquatic toxicity + 0.9100 91.00%

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 95.97% 91.11%
CHEMBL4208 P20618 Proteasome component C5 91.93% 90.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.33% 99.17%
CHEMBL2535 P11166 Glucose transporter 90.99% 98.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.96% 96.09%
CHEMBL1255126 O15151 Protein Mdm4 88.08% 90.20%
CHEMBL3194 P02766 Transthyretin 87.93% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.47% 86.33%

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.
Acer rubrum
Aframomum daniellii
Alchornea cordifolia
Alstonia angustiloba
Amphiachyris dracunculoides
Annona cherimola
Anthemis auriculata
Aristolochia foveolata
Aristolochia kaempferi
Aristolochia manshuriensis
Aristolochia zollingeriana
Atalantia wightii
Baccharis grandicapitulata
Balanophora japonica
Beesia calthifolia
Begonia nantoensis
Boschniakia rossica
Botrychium ternatum
Bursera kerberi
Calamus draco
Cestrum parqui
Clerodendrum trichotomum
Clinacanthus nutans
Corydalis persica
Corynanthe pachyceras
Cota tinctoria
Crocus sativus
Crotalaria stolzii
Curcuma aeruginosa
Cynoglossum amabile
Delphinium giraldii
Eucalyptus albens
Euonymus fortunei
Euploca racemosa
Excoecaria acerifolia
Fibraurea tinctoria
Garrya laurifolia
Glycosmis pseudoracemosa
Goupia glabra
Hedysarum gmelinii
Helenium integrifolium
Hibiscus taiwanensis
Houttuynia cordata
Hovenia dulcis
Iphiona grantioides
Juniperus horizontalis
Juniperus scopulorum
Laggera alata
Lasianthaea podocephala
Lathyrus tingitanus
Liriodendron tulipifera
Litsea hypophaea
Lupinus cosentinii
Medinilla magnifica
Melampodium leucanthum
Melicope semecarpifolia
Mesua ferrea
Moringa oleifera
Myrica pensylvanica
Neopallasia pectinata
Onobrychis bobrovii
Papaver persicum
Papaver pseudocanescens
Pellacalyx axillaris
Peperomia filiformis
Petteria ramentacea
Phlomis crinita
Phyllanthus oligospermus
Piptostigma fugax
Plectranthus caninus
Psidium acutangulum
Pyrolirion flavum
Rauvolfia salicifolia
Renealmia alpinia
Rhinacanthus nasutus
Rhododendron mucronulatum
Senecio cathcartensis
Sequoia sempervirens
Sesamum indicum
Seseli libanotis
Sideritis dasygnaphala
Spiraea formosana
Stellaria media
Strychnos spinosa
Syncarpha gnaphaloides
Tamarix aphylla
Taraxacum mongolicum
Tephroseris kirilowii
Tephroseris palustris
Tetradium glabrifolium
Tetragonotheca repanda
Trichocolea tomentella
Vitex trifolia subsp. litoralis
Zingiber officinale

Cross-Links

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PubChem 19844
NPASS NPC159418
LOTUS LTS0253904
wikiData Q27097897