Chalciporone

Details

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Internal ID a079aee1-071c-4da3-868e-a535500db04e
Taxonomy Organoheterocyclic compounds > Azepines
IUPAC Name (6E,8E)-9-(2-methyl-2H-azepin-7-yl)nona-6,8-dien-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H21NO/c1-3-16(18)13-7-5-4-6-11-15-12-9-8-10-14(2)17-15/h4-6,8-12,14H,3,7,13H2,1-2H3/b5-4+,11-6+
InChI Key YHYHJUHRELVMJW-LJIKRCSCSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C16H21NO
Molecular Weight 243.34 g/mol
Exact Mass 243.162314293 g/mol
Topological Polar Surface Area (TPSA) 29.40 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.81
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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(6E,8E)-9-(2-methyl-2H-azepin-7-yl)nona-6,8-dien-3-one
SCHEMBL19580242
CHEBI:187737
DTXSID501193247
(6E,8E)-(-)-9-(2-Methyl-2H-azepin-7-yl)-6,8-nonadien-3-one
112448-74-5

2D Structure

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2D Structure of Chalciporone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9935 99.35%
Caco-2 + 0.8426 84.26%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.3868 38.68%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8641 86.41%
OATP1B3 inhibitior + 0.9458 94.58%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.7962 79.62%
P-glycoprotein inhibitior - 0.9663 96.63%
P-glycoprotein substrate - 0.7828 78.28%
CYP3A4 substrate - 0.5154 51.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8540 85.40%
CYP3A4 inhibition - 0.9092 90.92%
CYP2C9 inhibition - 0.8793 87.93%
CYP2C19 inhibition - 0.8232 82.32%
CYP2D6 inhibition - 0.8501 85.01%
CYP1A2 inhibition + 0.6088 60.88%
CYP2C8 inhibition - 0.6566 65.66%
CYP inhibitory promiscuity - 0.8101 81.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.5998 59.98%
Eye corrosion - 0.6061 60.61%
Eye irritation - 0.9062 90.62%
Skin irritation + 0.6085 60.85%
Skin corrosion - 0.6125 61.25%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3652 36.52%
Micronuclear - 0.8200 82.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation + 0.5107 51.07%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.7778 77.78%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7002 70.02%
Acute Oral Toxicity (c) III 0.6727 67.27%
Estrogen receptor binding - 0.5618 56.18%
Androgen receptor binding - 0.6928 69.28%
Thyroid receptor binding - 0.8112 81.12%
Glucocorticoid receptor binding - 0.6302 63.02%
Aromatase binding - 0.5405 54.05%
PPAR gamma - 0.5459 54.59%
Honey bee toxicity - 0.9485 94.85%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity - 0.7566 75.66%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.60% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.63% 99.17%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 88.44% 87.67%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.45% 89.34%
CHEMBL2581 P07339 Cathepsin D 85.76% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.66% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 81.40% 94.73%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 21725394
LOTUS LTS0264806
wikiData Q105348675