2-(1',5'-Heptadienyl)-3,6-dihydroxy-5-(3"-methyl-2"-butenyl)benzaldehyde

Details

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Internal ID 30919222-c6ed-415e-9d8b-03a3f2643bcd
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Quinone and hydroquinone lipids > Prenylated hydroquinones
IUPAC Name 2-[(1E,5E)-hepta-1,5-dienyl]-3,6-dihydroxy-5-(3-methylbut-2-enyl)benzaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H24O3/c1-4-5-6-7-8-9-16-17(13-20)19(22)15(12-18(16)21)11-10-14(2)3/h4-5,8-10,12-13,21-22H,6-7,11H2,1-3H3/b5-4+,9-8+
InChI Key YMWWYKZCNJAKQU-KQWYESAVSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O3
Molecular Weight 300.40 g/mol
Exact Mass 300.17254462 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.79
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(1',5'-Heptadienyl)-3,6-dihydroxy-5-(3"-methyl-2"-butenyl)benzaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.6404 64.04%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.8701 87.01%
OATP2B1 inhibitior - 0.7144 71.44%
OATP1B1 inhibitior + 0.7369 73.69%
OATP1B3 inhibitior + 0.9472 94.72%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7190 71.90%
P-glycoprotein inhibitior - 0.5969 59.69%
P-glycoprotein substrate - 0.8036 80.36%
CYP3A4 substrate - 0.5336 53.36%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8078 80.78%
CYP3A4 inhibition - 0.6205 62.05%
CYP2C9 inhibition + 0.8308 83.08%
CYP2C19 inhibition + 0.8179 81.79%
CYP2D6 inhibition - 0.6765 67.65%
CYP1A2 inhibition + 0.8512 85.12%
CYP2C8 inhibition - 0.8296 82.96%
CYP inhibitory promiscuity + 0.7871 78.71%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7662 76.62%
Carcinogenicity (trinary) Non-required 0.6703 67.03%
Eye corrosion - 0.9600 96.00%
Eye irritation - 0.5370 53.70%
Skin irritation - 0.5370 53.70%
Skin corrosion - 0.8367 83.67%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7498 74.98%
Micronuclear - 0.7900 79.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.6836 68.36%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6418 64.18%
Acute Oral Toxicity (c) III 0.7474 74.74%
Estrogen receptor binding + 0.9161 91.61%
Androgen receptor binding + 0.5712 57.12%
Thyroid receptor binding + 0.7067 70.67%
Glucocorticoid receptor binding + 0.8496 84.96%
Aromatase binding + 0.7648 76.48%
PPAR gamma + 0.9594 95.94%
Honey bee toxicity - 0.9125 91.25%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9900 99.00%

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
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 98.35% 98.11%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.21% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.46% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 93.23% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.86% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.46% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.13% 96.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.40% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.75% 86.33%
CHEMBL1951 P21397 Monoamine oxidase A 81.53% 91.49%

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 25111561
LOTUS LTS0254666
wikiData Q75052926