3-Hydroxy-4-methoxybenzoic acid

Details

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Internal ID 76d911f9-8685-4757-b4a6-6b4a0ddc005b
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > P-methoxybenzoic acids and derivatives
IUPAC Name 3-hydroxy-4-methoxybenzoic acid
SMILES (Canonical) COC1=C(C=C(C=C1)C(=O)O)O
SMILES (Isomeric) COC1=C(C=C(C=C1)C(=O)O)O
InChI InChI=1S/C8H8O4/c1-12-7-3-2-5(8(10)11)4-6(7)9/h2-4,9H,1H3,(H,10,11)
InChI Key LBKFGYZQBSGRHY-UHFFFAOYSA-N
Popularity 217 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O4
Molecular Weight 168.15 g/mol
Exact Mass 168.04225873 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.10
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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Isovanillic acid
645-08-9
3-Hydroxy-p-anisic acid
Acide isovanillique
3-Hydroxyanisic acid
Benzoic acid, 3-hydroxy-4-methoxy-
p-Anisic acid, 3-hydroxy-
EINECS 211-430-5
MFCD00002507
A8D1DUX2PR
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-Hydroxy-4-methoxybenzoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9758 97.58%
Caco-2 + 0.6757 67.57%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.8990 89.90%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9648 96.48%
OATP1B3 inhibitior + 0.9707 97.07%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9742 97.42%
P-glycoprotein inhibitior - 0.9816 98.16%
P-glycoprotein substrate - 0.9687 96.87%
CYP3A4 substrate - 0.7259 72.59%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8470 84.70%
CYP3A4 inhibition - 0.9711 97.11%
CYP2C9 inhibition - 0.8125 81.25%
CYP2C19 inhibition - 0.8249 82.49%
CYP2D6 inhibition - 0.9702 97.02%
CYP1A2 inhibition - 0.8864 88.64%
CYP2C8 inhibition + 0.5363 53.63%
CYP inhibitory promiscuity - 0.8904 89.04%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.7026 70.26%
Carcinogenicity (trinary) Non-required 0.6294 62.94%
Eye corrosion + 0.6939 69.39%
Eye irritation + 0.9896 98.96%
Skin irritation + 0.7744 77.44%
Skin corrosion - 0.8786 87.86%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8247 82.47%
Micronuclear + 0.7000 70.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.8599 85.99%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.4923 49.23%
Estrogen receptor binding - 0.8103 81.03%
Androgen receptor binding - 0.8462 84.62%
Thyroid receptor binding - 0.8914 89.14%
Glucocorticoid receptor binding - 0.8030 80.30%
Aromatase binding - 0.6515 65.15%
PPAR gamma - 0.6715 67.15%
Honey bee toxicity - 0.9748 97.48%
Biodegradation + 0.7250 72.50%
Crustacea aquatic toxicity - 0.9400 94.00%
Fish aquatic toxicity + 0.8939 89.39%

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
CHEMBL3194 P02766 Transthyretin 96.28% 90.71%
CHEMBL1255126 O15151 Protein Mdm4 94.97% 90.20%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.08% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.20% 99.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.71% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.51% 96.09%
CHEMBL4208 P20618 Proteasome component C5 86.57% 90.00%
CHEMBL2535 P11166 Glucose transporter 86.31% 98.75%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 81.65% 94.42%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.12% 96.00%

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.
Acacia confusa
Alstonia angustiloba
Amphiachyris dracunculoides
Annona cherimola
Annona purpurea
Arachis hypogaea
Aristolochia gehrtii
Aristolochia kaempferi
Asarum heterotropoides
Asarum sieboldii
Baccharis grandicapitulata
Beesia calthifolia
Boschniakia rossica
Botrychium ternatum
Bursera kerberi
Calophyllum polyanthum
Campsis grandiflora
Cassia fistula
Centaurea spruneri
Cheniella glauca
Citrus × aurantium
Clerodendrum trichotomum
Clinacanthus nutans
Cota palaestina
Crocus sativus
Crotalaria stolzii
Curcuma aeruginosa
Delphinium giraldii
Eucalyptus albens
Euonymus fortunei
Euphorbia polycaulis
Euploca racemosa
Galinsoga quadriradiata
Ginkgo biloba
Hedysarum gmelinii
Helenium integrifolium
Hypericum erectum
Ilex pubescens
Imperata cylindrica
Jatropha curcas
Juniperus scopulorum
Knoxia roxburghii
Lasianthaea podocephala
Leucaena leucocephala
Lupinus cosentinii
Melampodium leucanthum
Microcos paniculata
Muntingia calabura
Myrica pensylvanica
Neopallasia pectinata
Paeonia suffruticosa
Panax notoginseng
Papaver pseudocanescens
Parmentiera cereifera
Pellacalyx axillaris
Peperomia filiformis
Perilla frutescens
Perilla frutescens var. crispa
Persea americana
Phlomis crinita
Pinus pinaster
Psammosilene tunicoides
Psidium acutangulum
Pteris multifida
Pyrolirion flavum
Renealmia alpinia
Rhododendron mucronulatum
Santalum album
Scrophularia frutescens
Scrophularia ningpoensis
Seseli libanotis
Sideritis dasygnaphala
Soroseris hookeriana
Stellaria media
Synsepalum dulcificum
Tephroseris kirilowii
Tephroseris palustris
Vitis vinifera
Zanthoxylum bungeanum

Cross-Links

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PubChem 12575
NPASS NPC283823
LOTUS LTS0247446
wikiData Q1674563