(3S,8R,9R,10S)-10-chloroheptadec-1-en-4,6-diyne-3,8,9-triol

Details

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Internal ID 232a4430-85ae-4503-832c-725db21bc76f
Taxonomy Organohalogen compounds > Halohydrins > Chlorohydrins
IUPAC Name (3S,8R,9R,10S)-10-chloroheptadec-1-en-4,6-diyne-3,8,9-triol
SMILES (Canonical) CCCCCCCC(C(C(C#CC#CC(C=C)O)O)O)Cl
SMILES (Isomeric) CCCCCCC[C@@H]([C@@H]([C@@H](C#CC#C[C@H](C=C)O)O)O)Cl
InChI InChI=1S/C17H25ClO3/c1-3-5-6-7-8-12-15(18)17(21)16(20)13-10-9-11-14(19)4-2/h4,14-17,19-21H,2-3,5-8,12H2,1H3/t14-,15-,16+,17-/m0/s1
InChI Key VKOLPKBPPQVWIT-NXOAAHMSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H25ClO3
Molecular Weight 312.80 g/mol
Exact Mass 312.1492223 g/mol
Topological Polar Surface Area (TPSA) 60.70 Ų
XlogP 3.60
Atomic LogP (AlogP) 2.23
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (3S,8R,9R,10S)-10-chloroheptadec-1-en-4,6-diyne-3,8,9-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9718 97.18%
Caco-2 - 0.6856 68.56%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6336 63.36%
OATP2B1 inhibitior - 0.8551 85.51%
OATP1B1 inhibitior + 0.8873 88.73%
OATP1B3 inhibitior + 0.9294 92.94%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8612 86.12%
P-glycoprotein inhibitior - 0.8747 87.47%
P-glycoprotein substrate - 0.7468 74.68%
CYP3A4 substrate + 0.5151 51.51%
CYP2C9 substrate - 0.7982 79.82%
CYP2D6 substrate - 0.7680 76.80%
CYP3A4 inhibition - 0.7828 78.28%
CYP2C9 inhibition - 0.7309 73.09%
CYP2C19 inhibition - 0.6637 66.37%
CYP2D6 inhibition - 0.8395 83.95%
CYP1A2 inhibition - 0.5245 52.45%
CYP2C8 inhibition - 0.7959 79.59%
CYP inhibitory promiscuity - 0.6599 65.99%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6335 63.35%
Carcinogenicity (trinary) Non-required 0.6369 63.69%
Eye corrosion - 0.7916 79.16%
Eye irritation - 0.9307 93.07%
Skin irritation - 0.6862 68.62%
Skin corrosion - 0.7370 73.70%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6860 68.60%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.6361 63.61%
skin sensitisation + 0.6934 69.34%
Respiratory toxicity - 0.6889 68.89%
Reproductive toxicity - 0.8116 81.16%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity + 0.7346 73.46%
Acute Oral Toxicity (c) III 0.5586 55.86%
Estrogen receptor binding + 0.7255 72.55%
Androgen receptor binding - 0.6114 61.14%
Thyroid receptor binding + 0.7498 74.98%
Glucocorticoid receptor binding + 0.8383 83.83%
Aromatase binding + 0.6465 64.65%
PPAR gamma + 0.6234 62.34%
Honey bee toxicity - 0.8518 85.18%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6209 62.09%
Fish aquatic toxicity + 0.9939 99.39%

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
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 97.76% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 96.66% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 94.78% 97.29%
CHEMBL2581 P07339 Cathepsin D 93.65% 98.95%
CHEMBL1907 P15144 Aminopeptidase N 92.36% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.46% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 91.24% 89.63%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 91.01% 91.81%
CHEMBL2885 P07451 Carbonic anhydrase III 90.58% 87.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.32% 92.08%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 90.07% 95.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.86% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.42% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 85.19% 90.17%
CHEMBL240 Q12809 HERG 84.97% 89.76%
CHEMBL3359 P21462 Formyl peptide receptor 1 84.67% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 84.53% 94.73%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 83.16% 100.00%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.19% 89.34%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.18% 96.61%

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.
Niphogeton ternata

Cross-Links

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PubChem 162846773
LOTUS LTS0197370
wikiData Q105287955