beta-Sinensal

Details

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Internal ID 80156464-dcd0-4ecc-a37c-942413b2c85f
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E,6E)-2,6-dimethyl-10-methylidenedodeca-2,6,11-trienal
SMILES (Canonical) CC(=CCCC(=C)C=C)CCC=C(C)C=O
SMILES (Isomeric) C/C(=C\CCC(=C)C=C)/CC/C=C(\C)/C=O
InChI InChI=1S/C15H22O/c1-5-13(2)8-6-9-14(3)10-7-11-15(4)12-16/h5,9,11-12H,1-2,6-8,10H2,3-4H3/b14-9+,15-11+
InChI Key NOPLRNXKHZRXHT-YFVJMOTDSA-N
Popularity 5 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 4.80
Atomic LogP (AlogP) 4.38
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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sinensal
trans-beta-Sinensal
3779-62-2
60066-88-8
UNII-4C2WZT6IRL
2,6-Dimethyl-10-methylene-2,6,11-dodecatrienal
2,6-Dimethyl-10-methylenedodeca-2,6,11-trien-1-al
Orange terpenes
4C2WZT6IRL
Sinensal, beta-
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of beta-Sinensal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9911 99.11%
Caco-2 + 0.7387 73.87%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Lysosomes 0.3394 33.94%
OATP2B1 inhibitior - 0.8560 85.60%
OATP1B1 inhibitior + 0.9156 91.56%
OATP1B3 inhibitior + 0.9145 91.45%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.6658 66.58%
P-glycoprotein inhibitior - 0.9412 94.12%
P-glycoprotein substrate - 0.9064 90.64%
CYP3A4 substrate - 0.5468 54.68%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8311 83.11%
CYP3A4 inhibition - 0.9720 97.20%
CYP2C9 inhibition - 0.9302 93.02%
CYP2C19 inhibition - 0.9303 93.03%
CYP2D6 inhibition - 0.9587 95.87%
CYP1A2 inhibition - 0.6074 60.74%
CYP2C8 inhibition - 0.9309 93.09%
CYP inhibitory promiscuity - 0.7958 79.58%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.5899 58.99%
Eye corrosion + 0.8900 89.00%
Eye irritation + 0.8988 89.88%
Skin irritation + 0.8068 80.68%
Skin corrosion - 0.9282 92.82%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5164 51.64%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation + 0.9521 95.21%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.7887 78.87%
Acute Oral Toxicity (c) III 0.8492 84.92%
Estrogen receptor binding - 0.8933 89.33%
Androgen receptor binding - 0.8767 87.67%
Thyroid receptor binding - 0.7413 74.13%
Glucocorticoid receptor binding - 0.4666 46.66%
Aromatase binding - 0.5430 54.30%
PPAR gamma + 0.6301 63.01%
Honey bee toxicity - 0.8227 82.27%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9910 99.10%

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 87.33% 96.09%
CHEMBL4246 P42680 Tyrosine-protein kinase TEC 86.55% 82.05%
CHEMBL1829 O15379 Histone deacetylase 3 84.15% 95.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.02% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.34% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.30% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.31% 89.34%
CHEMBL4040 P28482 MAP kinase ERK2 82.01% 83.82%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.39% 90.24%

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.
Astrantia major
Citrus × aurantium

Cross-Links

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PubChem 5281535
NPASS NPC74859
LOTUS LTS0063357
wikiData Q27108641