(2R,4R)-16-Heptadecyne-1,2,4-triol

Details

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Internal ID f2b20149-e32d-4205-ad6a-bbdf927666b7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name (2R,4R)-heptadec-16-yne-1,2,4-triol
SMILES (Canonical) C#CCCCCCCCCCCCC(CC(CO)O)O
SMILES (Isomeric) C#CCCCCCCCCCCC[C@H](C[C@H](CO)O)O
InChI InChI=1S/C17H32O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-16(19)14-17(20)15-18/h1,16-20H,3-15H2/t16-,17-/m1/s1
InChI Key OHLQBKZXSJYBMK-IAGOWNOFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H32O3
Molecular Weight 284.40 g/mol
Exact Mass 284.23514488 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 4.30
Atomic LogP (AlogP) 3.01
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 14

Synonyms

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SCHEMBL18730915
DTXSID401298181
129099-93-0

2D Structure

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2D Structure of (2R,4R)-16-Heptadecyne-1,2,4-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6618 66.18%
Caco-2 - 0.6147 61.47%
Blood Brain Barrier - 0.7500 75.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.7165 71.65%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9550 95.50%
OATP1B3 inhibitior + 0.9527 95.27%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7458 74.58%
P-glycoprotein inhibitior - 0.9293 92.93%
P-glycoprotein substrate - 0.9047 90.47%
CYP3A4 substrate - 0.5660 56.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7292 72.92%
CYP3A4 inhibition - 0.9097 90.97%
CYP2C9 inhibition - 0.7962 79.62%
CYP2C19 inhibition - 0.8453 84.53%
CYP2D6 inhibition - 0.9126 91.26%
CYP1A2 inhibition - 0.7319 73.19%
CYP2C8 inhibition - 0.9664 96.64%
CYP inhibitory promiscuity - 0.9210 92.10%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6997 69.97%
Eye corrosion - 0.9048 90.48%
Eye irritation - 0.8571 85.71%
Skin irritation - 0.7172 71.72%
Skin corrosion - 0.9300 93.00%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3786 37.86%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6304 63.04%
skin sensitisation - 0.8311 83.11%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.9444 94.44%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5212 52.12%
Acute Oral Toxicity (c) IV 0.6853 68.53%
Estrogen receptor binding - 0.6097 60.97%
Androgen receptor binding - 0.8670 86.70%
Thyroid receptor binding + 0.6214 62.14%
Glucocorticoid receptor binding + 0.6308 63.08%
Aromatase binding - 0.7009 70.09%
PPAR gamma - 0.5704 57.04%
Honey bee toxicity - 0.7928 79.28%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6583 65.83%
Fish aquatic toxicity - 0.8993 89.93%

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 92.84% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.55% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 89.26% 89.63%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.25% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.87% 91.11%
CHEMBL2581 P07339 Cathepsin D 88.11% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.87% 99.17%
CHEMBL2885 P07451 Carbonic anhydrase III 82.49% 87.45%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.46% 95.17%
CHEMBL242 Q92731 Estrogen receptor beta 80.78% 98.35%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.61% 100.00%

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.
Persea americana

Cross-Links

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PubChem 14630627
LOTUS LTS0093122
wikiData Q105192137