2,3,5,6,7,15-Hexachloropentadec-14-en-4-ol

Details

Top
Internal ID bafd2257-6f8c-48de-ac45-53d051092839
Taxonomy Organohalogen compounds > Halohydrins > Chlorohydrins
IUPAC Name 2,3,5,6,7,15-hexachloropentadec-14-en-4-ol
SMILES (Canonical) CC(C(C(C(C(C(CCCCCCC=CCl)Cl)Cl)Cl)O)Cl)Cl
SMILES (Isomeric) CC(C(C(C(C(C(CCCCCCC=CCl)Cl)Cl)Cl)O)Cl)Cl
InChI InChI=1S/C15H24Cl6O/c1-10(17)12(19)15(22)14(21)13(20)11(18)8-6-4-2-3-5-7-9-16/h7,9-15,22H,2-6,8H2,1H3
InChI Key VQLAUCXPJDIMTF-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C15H24Cl6O
Molecular Weight 433.10 g/mol
Exact Mass 431.992881 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 7.00
Atomic LogP (AlogP) 6.50
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2,3,5,6,7,15-Hexachloropentadec-14-en-4-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 - 0.6600 66.00%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5666 56.66%
OATP2B1 inhibitior - 0.8564 85.64%
OATP1B1 inhibitior + 0.8763 87.63%
OATP1B3 inhibitior + 0.9466 94.66%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7322 73.22%
P-glycoprotein inhibitior - 0.7976 79.76%
P-glycoprotein substrate - 0.8018 80.18%
CYP3A4 substrate - 0.5108 51.08%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7460 74.60%
CYP3A4 inhibition - 0.9445 94.45%
CYP2C9 inhibition - 0.8177 81.77%
CYP2C19 inhibition - 0.6989 69.89%
CYP2D6 inhibition - 0.9404 94.04%
CYP1A2 inhibition - 0.5836 58.36%
CYP2C8 inhibition - 0.9204 92.04%
CYP inhibitory promiscuity - 0.7750 77.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) + 0.5656 56.56%
Carcinogenicity (trinary) Non-required 0.6067 60.67%
Eye corrosion + 0.9390 93.90%
Eye irritation - 0.9860 98.60%
Skin irritation + 0.6107 61.07%
Skin corrosion + 0.6472 64.72%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4830 48.30%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5091 50.91%
skin sensitisation + 0.6850 68.50%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.7889 78.89%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.5613 56.13%
Acute Oral Toxicity (c) III 0.5877 58.77%
Estrogen receptor binding + 0.7622 76.22%
Androgen receptor binding + 0.5347 53.47%
Thyroid receptor binding + 0.7805 78.05%
Glucocorticoid receptor binding + 0.7524 75.24%
Aromatase binding + 0.7799 77.99%
PPAR gamma + 0.6391 63.91%
Honey bee toxicity - 0.8956 89.56%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5338 53.38%
Fish aquatic toxicity + 0.7383 73.83%

Targets

Top

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
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 94.77% 89.34%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.64% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.12% 96.09%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 90.00% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.43% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 88.66% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 88.13% 94.73%
CHEMBL2581 P07339 Cathepsin D 87.96% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 85.27% 87.45%
CHEMBL3975 P09467 Fructose-1,6-bisphosphatase 84.52% 92.95%
CHEMBL1829 O15379 Histone deacetylase 3 84.10% 95.00%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 83.49% 92.88%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.34% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.01% 91.11%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 81.65% 95.71%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.33% 97.21%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 80.24% 85.94%
CHEMBL240 Q12809 HERG 80.18% 89.76%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 85217915
LOTUS LTS0074314
wikiData Q105291349