(2E,8E,10R)-10-hydroxypentadeca-2,8-dien-4,6-diynal

Details

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Internal ID 6bf11a62-a980-40d8-b8e4-d82f1094b1bc
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name (2E,8E,10R)-10-hydroxypentadeca-2,8-dien-4,6-diynal
SMILES (Canonical) CCCCCC(C=CC#CC#CC=CC=O)O
SMILES (Isomeric) CCCCC[C@H](/C=C/C#CC#C/C=C/C=O)O
InChI InChI=1S/C15H18O2/c1-2-3-9-12-15(17)13-10-7-5-4-6-8-11-14-16/h8,10-11,13-15,17H,2-3,9,12H2,1H3/b11-8+,13-10+/t15-/m1/s1
InChI Key DKHGWZAGTJTORV-KZLMLFTGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H18O2
Molecular Weight 230.30 g/mol
Exact Mass 230.130679813 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.25
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,8E,10R)-10-hydroxypentadeca-2,8-dien-4,6-diynal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9931 99.31%
Caco-2 - 0.6692 66.92%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.4981 49.81%
OATP2B1 inhibitior - 0.8540 85.40%
OATP1B1 inhibitior + 0.8824 88.24%
OATP1B3 inhibitior + 0.7968 79.68%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8745 87.45%
P-glycoprotein inhibitior - 0.9327 93.27%
P-glycoprotein substrate - 0.7860 78.60%
CYP3A4 substrate - 0.5305 53.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8352 83.52%
CYP3A4 inhibition - 0.8180 81.80%
CYP2C9 inhibition - 0.8552 85.52%
CYP2C19 inhibition - 0.8261 82.61%
CYP2D6 inhibition - 0.9171 91.71%
CYP1A2 inhibition + 0.8778 87.78%
CYP2C8 inhibition - 0.9046 90.46%
CYP inhibitory promiscuity - 0.7027 70.27%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6400 64.00%
Carcinogenicity (trinary) Non-required 0.6390 63.90%
Eye corrosion + 0.7304 73.04%
Eye irritation - 0.6935 69.35%
Skin irritation + 0.8525 85.25%
Skin corrosion + 0.7607 76.07%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6719 67.19%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.6048 60.48%
skin sensitisation + 0.9035 90.35%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity - 0.9421 94.21%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.5439 54.39%
Acute Oral Toxicity (c) III 0.4318 43.18%
Estrogen receptor binding - 0.5620 56.20%
Androgen receptor binding - 0.7969 79.69%
Thyroid receptor binding + 0.6134 61.34%
Glucocorticoid receptor binding - 0.6192 61.92%
Aromatase binding - 0.5279 52.79%
PPAR gamma - 0.5967 59.67%
Honey bee toxicity - 0.9425 94.25%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5221 52.21%
Fish aquatic toxicity + 0.8272 82.72%

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 96.13% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 93.94% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.34% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 93.31% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.27% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.99% 92.86%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 92.70% 85.94%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.06% 92.08%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.45% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 84.85% 94.73%
CHEMBL299 P17252 Protein kinase C alpha 84.22% 98.03%
CHEMBL256 P0DMS8 Adenosine A3 receptor 83.64% 95.93%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.58% 100.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 82.88% 91.81%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.82% 96.00%
CHEMBL4040 P28482 MAP kinase ERK2 82.24% 83.82%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.91% 100.00%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 81.48% 96.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.36% 97.25%

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.
Bupleurum falcatum

Cross-Links

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PubChem 162954903
LOTUS LTS0045009
wikiData Q104983252