Heptadeca-1,9-dien-4,6-diyne-3,8,11-triol

Details

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Internal ID 9faaedab-15b1-4bba-ad5e-82c686d0d8b7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name heptadeca-1,9-dien-4,6-diyne-3,8,11-triol
SMILES (Canonical) CCCCCCC(C=CC(C#CC#CC(C=C)O)O)O
SMILES (Isomeric) CCCCCCC(C=CC(C#CC#CC(C=C)O)O)O
InChI InChI=1S/C17H24O3/c1-3-5-6-7-11-16(19)13-14-17(20)12-9-8-10-15(18)4-2/h4,13-20H,2-3,5-7,11H2,1H3
InChI Key VAHRGQLBSHWDKX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H24O3
Molecular Weight 276.40 g/mol
Exact Mass 276.17254462 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 2.90
Atomic LogP (AlogP) 1.79
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Heptadeca-1,9-dien-4,6-diyne-3,8,11-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9810 98.10%
Caco-2 - 0.6134 61.34%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.5366 53.66%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.9117 91.17%
OATP1B3 inhibitior + 0.9100 91.00%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9202 92.02%
P-glycoprotein inhibitior - 0.8955 89.55%
P-glycoprotein substrate - 0.8049 80.49%
CYP3A4 substrate - 0.5392 53.92%
CYP2C9 substrate - 0.6079 60.79%
CYP2D6 substrate - 0.7470 74.70%
CYP3A4 inhibition - 0.6632 66.32%
CYP2C9 inhibition - 0.8397 83.97%
CYP2C19 inhibition - 0.8194 81.94%
CYP2D6 inhibition - 0.9106 91.06%
CYP1A2 inhibition + 0.6306 63.06%
CYP2C8 inhibition - 0.8284 82.84%
CYP inhibitory promiscuity - 0.6853 68.53%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6971 69.71%
Eye corrosion - 0.6794 67.94%
Eye irritation - 0.9005 90.05%
Skin irritation - 0.5552 55.52%
Skin corrosion - 0.7964 79.64%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6785 67.85%
Micronuclear - 0.9300 93.00%
Hepatotoxicity - 0.5117 51.17%
skin sensitisation + 0.7715 77.15%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.9228 92.28%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.4574 45.74%
Acute Oral Toxicity (c) III 0.4301 43.01%
Estrogen receptor binding + 0.6710 67.10%
Androgen receptor binding - 0.7927 79.27%
Thyroid receptor binding + 0.6765 67.65%
Glucocorticoid receptor binding + 0.7163 71.63%
Aromatase binding + 0.5885 58.85%
PPAR gamma + 0.6616 66.16%
Honey bee toxicity - 0.9080 90.80%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6320 63.20%
Fish aquatic toxicity + 0.9671 96.71%

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
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 94.89% 97.29%
CHEMBL2581 P07339 Cathepsin D 94.58% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 93.98% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 93.69% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 93.31% 85.94%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.08% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 91.97% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.85% 96.09%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 90.14% 91.81%
CHEMBL2885 P07451 Carbonic anhydrase III 87.93% 87.45%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.14% 95.17%
CHEMBL240 Q12809 HERG 86.75% 89.76%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.64% 100.00%
CHEMBL2996 Q05655 Protein kinase C delta 85.52% 97.79%
CHEMBL1907 P15144 Aminopeptidase N 85.30% 93.31%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 82.93% 96.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.86% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 82.84% 94.73%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 82.45% 85.40%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.21% 91.11%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.73% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 80.36% 90.17%

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.
Angelica japonica
Glehnia littoralis

Cross-Links

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PubChem 469610
LOTUS LTS0262906
wikiData Q105282728