(E,5R)-5-hydroxy-1,7-bis(4-hydroxyphenyl)hept-1-en-3-one

Details

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Internal ID ec434bff-4f70-4c47-bbb8-61d77e36ba8a
Taxonomy Phenylpropanoids and polyketides > Diarylheptanoids > Linear diarylheptanoids > Curcuminoids
IUPAC Name (E,5R)-5-hydroxy-1,7-bis(4-hydroxyphenyl)hept-1-en-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H20O4/c20-16-7-1-14(2-8-16)5-11-18(22)13-19(23)12-6-15-3-9-17(21)10-4-15/h1-5,7-11,19-21,23H,6,12-13H2/b11-5+/t19-/m1/s1
InChI Key CWFOAVBXINFPCW-PHRJPNOBSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H20O4
Molecular Weight 312.40 g/mol
Exact Mass 312.13615911 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.06
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E,5R)-5-hydroxy-1,7-bis(4-hydroxyphenyl)hept-1-en-3-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9903 99.03%
Caco-2 - 0.8246 82.46%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.8619 86.19%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9335 93.35%
OATP1B3 inhibitior + 0.9308 93.08%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.5924 59.24%
P-glycoprotein inhibitior - 0.8038 80.38%
P-glycoprotein substrate - 0.6999 69.99%
CYP3A4 substrate - 0.5582 55.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7777 77.77%
CYP3A4 inhibition + 0.7331 73.31%
CYP2C9 inhibition - 0.8004 80.04%
CYP2C19 inhibition - 0.5252 52.52%
CYP2D6 inhibition - 0.9012 90.12%
CYP1A2 inhibition - 0.5248 52.48%
CYP2C8 inhibition - 0.6050 60.50%
CYP inhibitory promiscuity - 0.5892 58.92%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.7939 79.39%
Carcinogenicity (trinary) Non-required 0.5879 58.79%
Eye corrosion - 0.9802 98.02%
Eye irritation + 0.5416 54.16%
Skin irritation - 0.7010 70.10%
Skin corrosion - 0.9696 96.96%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3624 36.24%
Micronuclear - 0.7182 71.82%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.6518 65.18%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.7694 76.94%
Acute Oral Toxicity (c) III 0.7408 74.08%
Estrogen receptor binding + 0.9092 90.92%
Androgen receptor binding + 0.8613 86.13%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6293 62.93%
Aromatase binding + 0.7263 72.63%
PPAR gamma + 0.7238 72.38%
Honey bee toxicity - 0.7530 75.30%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity + 0.9596 95.96%

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 95.39% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.20% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.96% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.47% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.47% 94.45%
CHEMBL3437 Q16853 Amine oxidase, copper containing 88.43% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.62% 86.33%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 86.38% 100.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.28% 96.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 85.67% 95.50%
CHEMBL206 P03372 Estrogen receptor alpha 85.14% 97.64%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.05% 95.56%
CHEMBL3194 P02766 Transthyretin 83.60% 90.71%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 83.32% 85.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.51% 89.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.81% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.61% 90.71%
CHEMBL3401 O75469 Pregnane X receptor 80.88% 94.73%

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.
Dioscorea nipponica

Cross-Links

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PubChem 73349024
NPASS NPC285350
LOTUS LTS0056394
wikiData Q104971224