(3S,4S,5E,11E)-trideca-5,11-dien-7,9-diyne-3,4-diol

Details

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Internal ID 901ea617-2dc3-448a-b8ae-d238acaac2a8
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (3S,4S,5E,11E)-trideca-5,11-dien-7,9-diyne-3,4-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H16O2/c1-3-5-6-7-8-9-10-11-13(15)12(14)4-2/h3,5,10-15H,4H2,1-2H3/b5-3+,11-10+/t12-,13-/m0/s1
InChI Key URMQBWJXOJNVHX-SFXSTHPXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H16O2
Molecular Weight 204.26 g/mol
Exact Mass 204.115029749 g/mol
Topological Polar Surface Area (TPSA) 40.50 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.26
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,4S,5E,11E)-trideca-5,11-dien-7,9-diyne-3,4-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9805 98.05%
Caco-2 - 0.9044 90.44%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.5543 55.43%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.8308 83.08%
OATP1B3 inhibitior + 0.9448 94.48%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8880 88.80%
P-glycoprotein inhibitior - 0.9529 95.29%
P-glycoprotein substrate - 0.9073 90.73%
CYP3A4 substrate - 0.6381 63.81%
CYP2C9 substrate - 0.7983 79.83%
CYP2D6 substrate - 0.7784 77.84%
CYP3A4 inhibition - 0.8424 84.24%
CYP2C9 inhibition - 0.7923 79.23%
CYP2C19 inhibition - 0.7859 78.59%
CYP2D6 inhibition - 0.9128 91.28%
CYP1A2 inhibition - 0.7324 73.24%
CYP2C8 inhibition - 0.9384 93.84%
CYP inhibitory promiscuity - 0.8272 82.72%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.5500 55.00%
Carcinogenicity (trinary) Non-required 0.6496 64.96%
Eye corrosion - 0.7072 70.72%
Eye irritation - 0.9400 94.00%
Skin irritation + 0.5629 56.29%
Skin corrosion - 0.5278 52.78%
Ames mutagenesis - 0.6637 66.37%
Human Ether-a-go-go-Related Gene inhibition - 0.5283 52.83%
Micronuclear - 0.8268 82.68%
Hepatotoxicity - 0.5197 51.97%
skin sensitisation + 0.7880 78.80%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity - 0.8778 87.78%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.4563 45.63%
Acute Oral Toxicity (c) III 0.7420 74.20%
Estrogen receptor binding - 0.5736 57.36%
Androgen receptor binding - 0.8272 82.72%
Thyroid receptor binding - 0.4934 49.34%
Glucocorticoid receptor binding - 0.5475 54.75%
Aromatase binding - 0.6517 65.17%
PPAR gamma - 0.7511 75.11%
Honey bee toxicity - 0.9048 90.48%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.8200 82.00%
Fish aquatic toxicity - 0.7872 78.72%

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
CHEMBL4040 P28482 MAP kinase ERK2 92.33% 83.82%
CHEMBL2581 P07339 Cathepsin D 89.85% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.93% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.61% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 80.59% 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.
Aethusa cynapium
Trollius europaeus

Cross-Links

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PubChem 163034433
LOTUS LTS0271368
wikiData Q105168198