p-Anisic acid

Details

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Internal ID 613567ec-a7c9-4760-9f39-344f29da0e28
Taxonomy Benzenoids > Benzene and substituted derivatives > Benzoic acids and derivatives > Methoxybenzoic acids and derivatives > P-methoxybenzoic acids and derivatives
IUPAC Name 4-methoxybenzoic acid
SMILES (Canonical) COC1=CC=C(C=C1)C(=O)O
SMILES (Isomeric) COC1=CC=C(C=C1)C(=O)O
InChI InChI=1S/C8H8O3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H,9,10)
InChI Key ZEYHEAKUIGZSGI-UHFFFAOYSA-N
Popularity 934 references in papers

Physical and Chemical Properties

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Molecular Formula C8H8O3
Molecular Weight 152.15 g/mol
Exact Mass 152.047344113 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 2.00
Atomic LogP (AlogP) 1.39
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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p-Anisic acid
100-09-4
ANISIC ACID
p-Methoxybenzoic acid
Draconic acid
4-Anisic acid
Benzoic acid, 4-methoxy-
ANISIC ACID, PARA
para-anisic acid
Anisic acid, p-isomer
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of p-Anisic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9958 99.58%
Caco-2 + 0.9460 94.60%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.9255 92.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9723 97.23%
OATP1B3 inhibitior + 0.9780 97.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9454 94.54%
P-glycoprotein inhibitior - 0.9833 98.33%
P-glycoprotein substrate - 0.9923 99.23%
CYP3A4 substrate - 0.7619 76.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8571 85.71%
CYP3A4 inhibition - 0.9761 97.61%
CYP2C9 inhibition - 0.9764 97.64%
CYP2C19 inhibition - 0.9503 95.03%
CYP2D6 inhibition - 0.9848 98.48%
CYP1A2 inhibition - 0.6776 67.76%
CYP2C8 inhibition - 0.8404 84.04%
CYP inhibitory promiscuity - 0.9640 96.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5659 56.59%
Carcinogenicity (trinary) Non-required 0.5851 58.51%
Eye corrosion + 0.8329 83.29%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.8579 85.79%
Skin corrosion - 0.8627 86.27%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8913 89.13%
Micronuclear - 0.5445 54.45%
Hepatotoxicity - 0.8750 87.50%
skin sensitisation - 0.9390 93.90%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.5939 59.39%
Acute Oral Toxicity (c) III 0.8243 82.43%
Estrogen receptor binding - 0.8590 85.90%
Androgen receptor binding - 0.6829 68.29%
Thyroid receptor binding - 0.8508 85.08%
Glucocorticoid receptor binding - 0.8734 87.34%
Aromatase binding - 0.6409 64.09%
PPAR gamma - 0.7555 75.55%
Honey bee toxicity - 0.9913 99.13%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity - 0.9600 96.00%
Fish aquatic toxicity + 0.7524 75.24%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL261 P00915 Carbonic anhydrase I 9060 nM
Ki
PMID: 21402476
CHEMBL205 P00918 Carbonic anhydrase II 8030 nM
Ki
PMID: 21402476

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL1293294 P51151 Ras-related protein Rab-9A 96.45% 87.67%
CHEMBL4208 P20618 Proteasome component C5 93.89% 90.00%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 91.81% 81.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.48% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.33% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.68% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.20% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 82.75% 90.17%
CHEMBL1907 P15144 Aminopeptidase N 80.00% 93.31%

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.
Abies alba
Aconitum forrestii
Aegle marmelos
Albizia julibrissin
Alkanna hirsutissima
Amsinckia menziesii
Amyris barbata
Anacardium occidentale
Anastatica hierochuntica
Anchusa officinalis
Angelica sinensis
Annona purpurea
Aquilaria sinensis
Asplenium adiantum-nigrum
Buddleja davidii
Calea megacephala
Calea pinnatifida
Capparis spinosa
Caryopteris mongholica
Chaenomeles sinensis
Chaenomeles speciosa
Chamaecrista greggii
Chromolaena subscandens
Clausena anisata
Colchicum speciosum
Cordyline indivisa
Corydalis cornuta
Cota palaestina
Cyathobasis fruticulosa
Dalbergia rubiginosa
Daphne mucronata
Delphinium campylocentrum
Delphinium giraldii
Disepalum plagioneurum
Distemonanthus benthamianus
Eremophila serrulata
Euphorbia aleppica
Euphorbia kansui
Ferula latipinna
Ferula sinaica
Ficus mucuso
Foeniculum vulgare
Grindelia hirsutula
Hakea salicifolia
Haloxylon salicornicum
Handroanthus impetiginosus
Illicium verum
Isatis tinctoria
Jasminum grandiflorum
Lagotis yunnanensis
Leucanthemum maximum
Licaria triandra
Limnophila rugosa
Lysionotus denticulosus
Mappia nimmoniana
Melaleuca uncinata
Mentha arvensis
Mesembryanthemum tortuosum
Momordica charantia
Nelumbo nucifera
Neolitsea hiiranensis
Nymphaea micrantha
Packera bellidifolia
Parthenium hysterophorus
Peperomia heyneana
Perovskia atriplicifolia
Persea indica
Phegopteris microstegia
Picris asplenioides subsp. asplenioides
Pimpinella anisum
Piper aduncum
Piper aequale
Piper kwashoense
Populus deltoides
Posidonia oceanica
Primula hirsuta
Pulicaria gnaphalodes
Pulicaria paludosa
Putranjiva roxburghii
Rhododendron dauricum
Rhododendron ferrugineum
Rodgersia podophylla
Rostrinucula dependens
Salsola collina
Salvia nubicola
Satureja atropatana
Scapania nemorea
Senecio scandens
Soroseris hookeriana
Taraxacum mongolicum
Trianthema portulacastrum
Vaccinium macrocarpon
Vallaris solanacea
Vanilla planifolia
Vanilla pompona
Viburnum dilatatum
Viscum coloratum
Vitex trifolia
Wurfbainia longiligularis
Wurfbainia villosa
Wurfbainia villosa var. xanthioides

Cross-Links

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PubChem 7478
NPASS NPC61779
ChEMBL CHEMBL21932
LOTUS LTS0123492
wikiData Q4566032