(20Z)-4,6,12,17,20,21,23,26-octachloropentacyclo[20.2.2.110,14.115,19.02,7]octacosa-1(25),2,4,6,10(28),11,13,15,17,19(27),20,22(26),23-tridecaene-5,13,16,24-tetrol

Details

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Internal ID d59b87da-0bcb-4801-b6c9-030a5ae64f4a
Taxonomy Benzenoids > Phenols > Halophenols
IUPAC Name (20Z)-4,6,12,17,20,21,23,26-octachloropentacyclo[20.2.2.110,14.115,19.02,7]octacosa-1(25),2,4,6,10(28),11,13,15,17,19(27),20,22(26),23-tridecaene-5,13,16,24-tetrol
SMILES (Canonical) C1CC2=C(C(=C(C=C2C3=CC(=C(C(=C3O)Cl)C(=C(C4=CC(=C(C(=C4)Cl)O)C5=C(C(=CC1=C5)Cl)O)Cl)Cl)Cl)Cl)O)Cl
SMILES (Isomeric) C1CC2=C(C(=C(C=C2C3=CC(=C(C(=C3O)Cl)/C(=C(\C4=CC(=C(C(=C4)Cl)O)C5=C(C(=CC1=C5)Cl)O)/Cl)/Cl)Cl)Cl)O)Cl
InChI InChI=1S/C28H14Cl8O4/c29-16-8-15-12-7-19(32)28(40)22(34)11(12)2-1-9-3-13(25(37)17(30)4-9)14-5-10(6-18(31)26(14)38)21(33)23(35)20(16)24(36)27(15)39/h3-8,37-40H,1-2H2/b23-21-
InChI Key PUVVUWIKKLCJMS-LNVKXUELSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H14Cl8O4
Molecular Weight 698.00 g/mol
Exact Mass 697.834130 g/mol
Topological Polar Surface Area (TPSA) 80.90 Ų
XlogP 10.90
Atomic LogP (AlogP) 11.17
H-Bond Acceptor 4
H-Bond Donor 4
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (20Z)-4,6,12,17,20,21,23,26-octachloropentacyclo[20.2.2.110,14.115,19.02,7]octacosa-1(25),2,4,6,10(28),11,13,15,17,19(27),20,22(26),23-tridecaene-5,13,16,24-tetrol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9792 97.92%
Caco-2 - 0.8090 80.90%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.8391 83.91%
OATP2B1 inhibitior + 0.5689 56.89%
OATP1B1 inhibitior + 0.8411 84.11%
OATP1B3 inhibitior + 0.9182 91.82%
MATE1 inhibitior - 0.6800 68.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9787 97.87%
P-glycoprotein inhibitior - 0.4595 45.95%
P-glycoprotein substrate - 0.7161 71.61%
CYP3A4 substrate + 0.5734 57.34%
CYP2C9 substrate - 0.8064 80.64%
CYP2D6 substrate - 0.6794 67.94%
CYP3A4 inhibition - 0.5455 54.55%
CYP2C9 inhibition + 0.9148 91.48%
CYP2C19 inhibition + 0.8476 84.76%
CYP2D6 inhibition - 0.7784 77.84%
CYP1A2 inhibition + 0.9237 92.37%
CYP2C8 inhibition + 0.6414 64.14%
CYP inhibitory promiscuity + 0.8275 82.75%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6203 62.03%
Carcinogenicity (trinary) Non-required 0.5037 50.37%
Eye corrosion - 0.9654 96.54%
Eye irritation - 0.8136 81.36%
Skin irritation + 0.5304 53.04%
Skin corrosion - 0.9324 93.24%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8234 82.34%
Micronuclear - 0.5700 57.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.5595 55.95%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.5990 59.90%
Acute Oral Toxicity (c) III 0.5688 56.88%
Estrogen receptor binding + 0.8727 87.27%
Androgen receptor binding + 0.7803 78.03%
Thyroid receptor binding + 0.7611 76.11%
Glucocorticoid receptor binding + 0.9007 90.07%
Aromatase binding + 0.6892 68.92%
PPAR gamma + 0.9430 94.30%
Honey bee toxicity - 0.8732 87.32%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6700 67.00%
Fish aquatic toxicity + 0.9966 99.66%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.43% 91.11%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 91.14% 95.34%
CHEMBL2581 P07339 Cathepsin D 91.12% 98.95%
CHEMBL5905 Q04828 Aldo-keto reductase family 1 member C1 89.91% 91.79%
CHEMBL242 Q92731 Estrogen receptor beta 88.31% 98.35%
CHEMBL1951 P21397 Monoamine oxidase A 88.09% 91.49%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.93% 86.33%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.67% 99.15%
CHEMBL226 P30542 Adenosine A1 receptor 86.88% 95.93%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 85.07% 83.57%
CHEMBL221 P23219 Cyclooxygenase-1 84.32% 90.17%
CHEMBL2056 P21728 Dopamine D1 receptor 83.41% 91.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.15% 96.09%
CHEMBL2083 P15090 Fatty acid binding protein adipocyte 82.89% 95.71%
CHEMBL1929 P47989 Xanthine dehydrogenase 82.89% 96.12%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 82.00% 96.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.86% 94.45%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.49% 95.78%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 80.79% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 80.07% 94.73%

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.
Lepidozia incurvata

Cross-Links

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PubChem 21576530
LOTUS LTS0248123
wikiData Q105215309