ar-Curcumen-15-al

Details

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Internal ID 9215cbad-50b6-48c6-9f24-c56c3fa7769d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 4-(6-methylhept-5-en-2-yl)benzaldehyde
SMILES (Canonical) CC(CCC=C(C)C)C1=CC=C(C=C1)C=O
SMILES (Isomeric) CC(CCC=C(C)C)C1=CC=C(C=C1)C=O
InChI InChI=1S/C15H20O/c1-12(2)5-4-6-13(3)15-9-7-14(11-16)8-10-15/h5,7-11,13H,4,6H2,1-3H3
InChI Key XVWGGKCJOXAGDW-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H20O
Molecular Weight 216.32 g/mol
Exact Mass 216.151415257 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.35
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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XVWGGKCJOXAGDW-UHFFFAOYSA-N
Q67879692

2D Structure

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2D Structure of ar-Curcumen-15-al

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9968 99.68%
Caco-2 + 0.9495 94.95%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Nucleus 0.3518 35.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8968 89.68%
OATP1B3 inhibitior + 0.8817 88.17%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5260 52.60%
P-glycoprotein inhibitior - 0.9719 97.19%
P-glycoprotein substrate - 0.8896 88.96%
CYP3A4 substrate - 0.7076 70.76%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7337 73.37%
CYP3A4 inhibition - 0.9491 94.91%
CYP2C9 inhibition - 0.8844 88.44%
CYP2C19 inhibition - 0.8450 84.50%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition - 0.5744 57.44%
CYP2C8 inhibition - 0.9917 99.17%
CYP inhibitory promiscuity - 0.5465 54.65%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.5800 58.00%
Eye corrosion - 0.7558 75.58%
Eye irritation + 0.6074 60.74%
Skin irritation + 0.8879 88.79%
Skin corrosion - 0.7353 73.53%
Ames mutagenesis - 0.8800 88.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6985 69.85%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5750 57.50%
skin sensitisation + 0.9602 96.02%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.4737 47.37%
Acute Oral Toxicity (c) III 0.8826 88.26%
Estrogen receptor binding - 0.7970 79.70%
Androgen receptor binding - 0.7084 70.84%
Thyroid receptor binding - 0.6891 68.91%
Glucocorticoid receptor binding - 0.6982 69.82%
Aromatase binding - 0.6349 63.49%
PPAR gamma - 0.6651 66.51%
Honey bee toxicity - 0.9365 93.65%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity + 0.9867 98.67%

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
CHEMBL2581 P07339 Cathepsin D 95.04% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.62% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 92.10% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.99% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.26% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.41% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.50% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.92% 90.71%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.86% 93.56%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 80.46% 85.30%

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.
Lantana camara

Cross-Links

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PubChem 10846393
LOTUS LTS0194294
wikiData Q67879692