cis-p-Coumaric acid

Details

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Internal ID 16fb27e2-c399-4f9c-a5be-8c40a99a0485
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Hydroxycinnamic acids and derivatives > Hydroxycinnamic acids
IUPAC Name (Z)-3-(4-hydroxyphenyl)prop-2-enoic acid
SMILES (Canonical) C1=CC(=CC=C1C=CC(=O)O)O
SMILES (Isomeric) C1=CC(=CC=C1/C=C\C(=O)O)O
InChI InChI=1S/C9H8O3/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-6,10H,(H,11,12)/b6-3-
InChI Key NGSWKAQJJWESNS-UTCJRWHESA-N
Popularity 93 references in papers

Physical and Chemical Properties

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Molecular Formula C9H8O3
Molecular Weight 164.16 g/mol
Exact Mass 164.047344113 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.49
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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cis-4-Hydroxycinnamic acid
4501-31-9
(Z)-p-Coumaric acid
cis-p-Cumaric acid
cis-p-Hydroxycinnamic acid
cis-4-coumaric acid
cis-p-Coumarinic acid
(Z)-3-(4-Hydroxyphenyl)-2-propenoic acid
cis-p-Coumarate
(Z)-3-(4-hydroxyphenyl)prop-2-enoic acid
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of cis-p-Coumaric acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 + 0.8533 85.33%
Blood Brain Barrier - 0.7750 77.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.8227 82.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9325 93.25%
OATP1B3 inhibitior + 0.9445 94.45%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9108 91.08%
P-glycoprotein inhibitior - 0.9890 98.90%
P-glycoprotein substrate - 0.9843 98.43%
CYP3A4 substrate - 0.7537 75.37%
CYP2C9 substrate - 0.6124 61.24%
CYP2D6 substrate - 0.8682 86.82%
CYP3A4 inhibition - 0.8693 86.93%
CYP2C9 inhibition - 0.9364 93.64%
CYP2C19 inhibition - 0.9116 91.16%
CYP2D6 inhibition - 0.9766 97.66%
CYP1A2 inhibition - 0.9458 94.58%
CYP2C8 inhibition - 0.6249 62.49%
CYP inhibitory promiscuity - 0.8913 89.13%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6105 61.05%
Carcinogenicity (trinary) Non-required 0.6034 60.34%
Eye corrosion + 0.6040 60.40%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.9245 92.45%
Skin corrosion - 0.8096 80.96%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8830 88.30%
Micronuclear + 0.5900 59.00%
Hepatotoxicity - 0.7378 73.78%
skin sensitisation + 0.8695 86.95%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.4692 46.92%
Acute Oral Toxicity (c) III 0.4898 48.98%
Estrogen receptor binding - 0.8610 86.10%
Androgen receptor binding + 0.5583 55.83%
Thyroid receptor binding - 0.8178 81.78%
Glucocorticoid receptor binding - 0.7008 70.08%
Aromatase binding - 0.7910 79.10%
PPAR gamma - 0.6443 64.43%
Honey bee toxicity - 0.9576 95.76%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9444 94.44%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL205 P00918 Carbonic anhydrase II 980 nM
Ki
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL206 P03372 Estrogen receptor alpha 92.50% 97.64%
CHEMBL3194 P02766 Transthyretin 90.77% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.97% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.67% 95.56%
CHEMBL242 Q92731 Estrogen receptor beta 89.50% 98.35%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.49% 86.33%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 84.39% 91.71%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.84% 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.
Aconitum carmichaelii
Aconitum japonicum
Ageratina areolaris
Albizia julibrissin
Alcea rosea
Allium sativum
Aloe africana
Aloe ferox
Aloe spicata
Aloe vera
Aristolochia contorta
Aristolochia debilis
Baccharis myrsinites
Boehmeria nivea
Carthamus tinctorius
Castanopsis fissa
Centella asiatica
Chelidonium majus
Cirsium japonicum
Citrus × aurantium
Citrus deliciosa
Citrus medica
Commelina communis
Cornus officinalis
Cremastra appendiculata
Delphinium venulosum
Dracocephalum ruyschiana
Eleutherococcus senticosus
Epimedium sagittatum
Eucommia ulmoides
Fagopyrum acutatum
Ginkgo biloba
Hippophae rhamnoides
Hoffmannia strigillosa
Hordeum vulgare
Imperata cylindrica
Inula japonica
Ipomoea nil
Ipomoea purpurea
Juglans regia
Lilium brownii
Lilium lancifolium
Lilium pumilum
Linum usitatissimum
Lonicera japonica
Lotus corniculatus subsp. corniculatus
Luffa aegyptiaca
Lycium barbarum
Lycium chinense
Medicago sativa
Melia azedarach
Morus alba
Morus indica
Nelumbo nucifera
Oryza sativa
Oxalis pes-caprae
Pentanema britannicum
Peperomia heyneana
Persicaria orientalis
Pleione bulbocodioides
Pleione yunnanensis
Populus tremuloides
Portulaca oleracea
Prunella vulgaris
Punica granatum
Ranunculus ternatus
Reynoutria japonica
Reynoutria multiflora
Rhodiola rosea
Rhododendron dauricum
Rosa chinensis
Rosa rugosa
Rubus chingii
Rubus coreanus
Rumex chalepensis
Rumex japonicus
Schisandra chinensis
Scleromitrion diffusum
Scrophularia buergeriana
Scrophularia ningpoensis
Scutellaria barbata
Senecio scandens
Solanum nigrum
Sparganium stoloniferum
Styrax benzoin
Styrax tonkinensis
Taraxacum coreanum
Taraxacum mongolicum
Taraxacum officinale
Taraxacum platycarpum
Taraxacum sinicum
Thymus quinquecostatus
Thymus vulgaris
Toxicodendron vernicifluum
Vigna angularis
Vigna umbellata
Ziziphus jujuba

Cross-Links

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PubChem 1549106
NPASS NPC32977
LOTUS LTS0181455
wikiData Q27102404