Selina-3,11-dien-14-al

Details

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Internal ID 894ef848-b838-4b82-bf21-b5378c700907
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (4aR,7R)-4a-methyl-7-prop-1-en-2-yl-4,5,6,7,8,8a-hexahydro-3H-naphthalene-1-carbaldehyde
SMILES (Canonical) CC(=C)C1CCC2(CCC=C(C2C1)C=O)C
SMILES (Isomeric) CC(=C)[C@@H]1CC[C@]2(CCC=C(C2C1)C=O)C
InChI InChI=1S/C15H22O/c1-11(2)12-6-8-15(3)7-4-5-13(10-16)14(15)9-12/h5,10,12,14H,1,4,6-9H2,2-3H3/t12-,14?,15-/m1/s1
InChI Key HAGXJRWOGHAEIY-SULGFLJSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 4.50
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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HAGXJRWOGHAEIY-SULGFLJSSA-N

2D Structure

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2D Structure of Selina-3,11-dien-14-al

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8155 81.55%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Lysosomes 0.5595 55.95%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9204 92.04%
OATP1B3 inhibitior + 0.8857 88.57%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.7861 78.61%
P-glycoprotein inhibitior - 0.9375 93.75%
P-glycoprotein substrate - 0.8383 83.83%
CYP3A4 substrate + 0.5392 53.92%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8425 84.25%
CYP3A4 inhibition - 0.7814 78.14%
CYP2C9 inhibition - 0.7511 75.11%
CYP2C19 inhibition - 0.6030 60.30%
CYP2D6 inhibition - 0.9291 92.91%
CYP1A2 inhibition - 0.7611 76.11%
CYP2C8 inhibition - 0.8412 84.12%
CYP inhibitory promiscuity - 0.7112 71.12%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8000 80.00%
Carcinogenicity (trinary) Non-required 0.5300 53.00%
Eye corrosion - 0.8981 89.81%
Eye irritation - 0.5668 56.68%
Skin irritation - 0.6099 60.99%
Skin corrosion - 0.9734 97.34%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6534 65.34%
Micronuclear - 0.9200 92.00%
Hepatotoxicity + 0.5348 53.48%
skin sensitisation + 0.8683 86.83%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6067 60.67%
Acute Oral Toxicity (c) III 0.8415 84.15%
Estrogen receptor binding - 0.7498 74.98%
Androgen receptor binding - 0.7184 71.84%
Thyroid receptor binding - 0.7035 70.35%
Glucocorticoid receptor binding - 0.6151 61.51%
Aromatase binding - 0.5907 59.07%
PPAR gamma - 0.6249 62.49%
Honey bee toxicity - 0.8031 80.31%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.04% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.76% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.87% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.67% 95.56%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.90% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.23% 97.09%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.07% 92.94%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 83.39% 85.30%
CHEMBL218 P21554 Cannabinoid CB1 receptor 83.07% 96.61%
CHEMBL1951 P21397 Monoamine oxidase A 82.87% 91.49%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.77% 95.89%
CHEMBL4208 P20618 Proteasome component C5 81.39% 90.00%

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.
Aquilaria malaccensis
Aquilaria sinensis

Cross-Links

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PubChem 6431304
NPASS NPC286570