Cucullamide

Details

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Internal ID 8263799e-cae3-454a-9d9b-81b962e9035d
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acid amides
IUPAC Name [(E)-3-methyl-4-oxo-4-[4-[[(E)-3-phenylprop-2-enoyl]amino]butylamino]but-2-enyl] 4-methoxybenzoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H30N2O5/c1-20(16-19-33-26(31)22-11-13-23(32-2)14-12-22)25(30)28-18-7-6-17-27-24(29)15-10-21-8-4-3-5-9-21/h3-5,8-16H,6-7,17-19H2,1-2H3,(H,27,29)(H,28,30)/b15-10+,20-16+
InChI Key UXEVFTFWWUXKCP-XRSREISPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H30N2O5
Molecular Weight 450.50 g/mol
Exact Mass 450.21547206 g/mol
Topological Polar Surface Area (TPSA) 93.70 Ų
XlogP 3.80
Atomic LogP (AlogP) 3.52
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cucullamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9599 95.99%
Caco-2 - 0.7344 73.44%
Blood Brain Barrier + 0.5911 59.11%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8334 83.34%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.8930 89.30%
OATP1B3 inhibitior + 0.9379 93.79%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.8788 87.88%
P-glycoprotein inhibitior + 0.8960 89.60%
P-glycoprotein substrate - 0.5103 51.03%
CYP3A4 substrate + 0.5886 58.86%
CYP2C9 substrate - 0.6150 61.50%
CYP2D6 substrate - 0.8645 86.45%
CYP3A4 inhibition + 0.6479 64.79%
CYP2C9 inhibition - 0.5981 59.81%
CYP2C19 inhibition - 0.6037 60.37%
CYP2D6 inhibition + 0.5380 53.80%
CYP1A2 inhibition - 0.7386 73.86%
CYP2C8 inhibition + 0.7996 79.96%
CYP inhibitory promiscuity + 0.6192 61.92%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8328 83.28%
Carcinogenicity (trinary) Non-required 0.6223 62.23%
Eye corrosion - 0.9925 99.25%
Eye irritation - 0.9458 94.58%
Skin irritation - 0.7908 79.08%
Skin corrosion - 0.9495 94.95%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9038 90.38%
Micronuclear + 0.5700 57.00%
Hepatotoxicity - 0.5875 58.75%
skin sensitisation - 0.8873 88.73%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.7313 73.13%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7392 73.92%
Acute Oral Toxicity (c) III 0.6984 69.84%
Estrogen receptor binding + 0.6565 65.65%
Androgen receptor binding + 0.8822 88.22%
Thyroid receptor binding + 0.5955 59.55%
Glucocorticoid receptor binding - 0.4927 49.27%
Aromatase binding - 0.5813 58.13%
PPAR gamma + 0.6477 64.77%
Honey bee toxicity - 0.9326 93.26%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 0.9742 97.42%

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 97.53% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.89% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.70% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 96.42% 90.17%
CHEMBL3192 Q9BY41 Histone deacetylase 8 95.65% 93.99%
CHEMBL2581 P07339 Cathepsin D 95.01% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.58% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.26% 99.17%
CHEMBL4208 P20618 Proteasome component C5 92.53% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.08% 95.56%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 90.82% 95.50%
CHEMBL2179 P04062 Beta-glucocerebrosidase 88.61% 85.31%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 88.13% 96.67%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 85.39% 81.11%
CHEMBL3401 O75469 Pregnane X receptor 85.31% 94.73%
CHEMBL3492 P49721 Proteasome Macropain subunit 83.43% 90.24%
CHEMBL5028 O14672 ADAM10 83.09% 97.50%
CHEMBL5261 Q7L7X3 Serine/threonine-protein kinase TAO1 83.02% 89.33%
CHEMBL240 Q12809 HERG 82.81% 89.76%
CHEMBL2535 P11166 Glucose transporter 81.96% 98.75%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.07% 97.21%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.49% 91.07%

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.
Aglaia cucullata

Cross-Links

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PubChem 46873470
LOTUS LTS0254012
wikiData Q105244665