Chiricanine C

Details

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Internal ID db913bf8-79aa-4aed-897a-d5c41b9055e1
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name 3-methoxy-2,4-bis(3-methylbut-2-enyl)-5-[(E)-2-phenylethenyl]phenol
SMILES (Canonical) CC(=CCC1=C(C(=C(C=C1C=CC2=CC=CC=C2)O)CC=C(C)C)OC)C
SMILES (Isomeric) CC(=CCC1=C(C(=C(C=C1/C=C/C2=CC=CC=C2)O)CC=C(C)C)OC)C
InChI InChI=1S/C25H30O2/c1-18(2)11-15-22-21(14-13-20-9-7-6-8-10-20)17-24(26)23(25(22)27-5)16-12-19(3)4/h6-14,17,26H,15-16H2,1-5H3/b14-13+
InChI Key ZMMOCDBCJOUFDQ-BUHFOSPRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C25H30O2
Molecular Weight 362.50 g/mol
Exact Mass 362.224580195 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 7.70
Atomic LogP (AlogP) 6.59
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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Chiricanone C
CHEMBL512168

2D Structure

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2D Structure of Chiricanine C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.8045 80.45%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8225 82.25%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.8347 83.47%
OATP1B3 inhibitior + 0.9206 92.06%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9727 97.27%
P-glycoprotein inhibitior + 0.8908 89.08%
P-glycoprotein substrate - 0.8935 89.35%
CYP3A4 substrate - 0.5541 55.41%
CYP2C9 substrate + 0.6048 60.48%
CYP2D6 substrate + 0.3626 36.26%
CYP3A4 inhibition - 0.8863 88.63%
CYP2C9 inhibition - 0.5532 55.32%
CYP2C19 inhibition + 0.8522 85.22%
CYP2D6 inhibition - 0.8166 81.66%
CYP1A2 inhibition + 0.5884 58.84%
CYP2C8 inhibition + 0.5814 58.14%
CYP inhibitory promiscuity + 0.8460 84.60%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7226 72.26%
Carcinogenicity (trinary) Non-required 0.7153 71.53%
Eye corrosion - 0.9851 98.51%
Eye irritation - 0.5973 59.73%
Skin irritation - 0.8159 81.59%
Skin corrosion - 0.9360 93.60%
Ames mutagenesis + 0.5446 54.46%
Human Ether-a-go-go-Related Gene inhibition + 0.8308 83.08%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.5400 54.00%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.7843 78.43%
Acute Oral Toxicity (c) III 0.8019 80.19%
Estrogen receptor binding + 0.9132 91.32%
Androgen receptor binding + 0.8046 80.46%
Thyroid receptor binding + 0.7813 78.13%
Glucocorticoid receptor binding + 0.8434 84.34%
Aromatase binding + 0.6542 65.42%
PPAR gamma + 0.9309 93.09%
Honey bee toxicity - 0.8994 89.94%
Biodegradation - 0.9500 95.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9967 99.67%

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 99.20% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 97.03% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.93% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.37% 93.99%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 90.69% 94.62%
CHEMBL2581 P07339 Cathepsin D 90.08% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.22% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 88.90% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.26% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.61% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.69% 94.45%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 82.88% 94.08%
CHEMBL221 P23219 Cyclooxygenase-1 81.55% 90.17%
CHEMBL3194 P02766 Transthyretin 80.55% 90.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.45% 95.50%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.21% 96.95%

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.
Lonchocarpus chiricanus
Rheum palmatum

Cross-Links

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PubChem 10893817
NPASS NPC105031
LOTUS LTS0023740
wikiData Q105379523