(20E)-4,6,23-trichloro-13-methoxypentacyclo[20.2.2.110,14.115,19.02,7]octacosa-1(24),2,4,6,10(28),11,13,15,17,19(27),20,22,25-tridecaene-5,16,24-triol

Details

Top
Internal ID d6080454-e68f-4eac-b4e6-ee692ae78b97
Taxonomy Benzenoids > Phenols > Halophenols
IUPAC Name (20E)-4,6,23-trichloro-13-methoxypentacyclo[20.2.2.110,14.115,19.02,7]octacosa-1(24),2,4,6,10(28),11,13,15,17,19(27),20,22,25-tridecaene-5,16,24-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C29H21Cl3O4/c1-36-25-11-5-16-3-8-18-20(14-23(30)29(35)27(18)32)19-9-7-17(26(31)28(19)34)6-2-15-4-10-24(33)21(12-15)22(25)13-16/h2,4-7,9-14,33-35H,3,8H2,1H3/b6-2+
InChI Key YHYFZZPAXLZZLU-QHHAFSJGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C29H21Cl3O4
Molecular Weight 539.80 g/mol
Exact Mass 538.050542 g/mol
Topological Polar Surface Area (TPSA) 69.90 Ų
XlogP 8.70
Atomic LogP (AlogP) 8.38
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (20E)-4,6,23-trichloro-13-methoxypentacyclo[20.2.2.110,14.115,19.02,7]octacosa-1(24),2,4,6,10(28),11,13,15,17,19(27),20,22,25-tridecaene-5,16,24-triol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9817 98.17%
Caco-2 - 0.6875 68.75%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8469 84.69%
OATP2B1 inhibitior - 0.8542 85.42%
OATP1B1 inhibitior + 0.8673 86.73%
OATP1B3 inhibitior + 0.9502 95.02%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9928 99.28%
P-glycoprotein inhibitior + 0.6835 68.35%
P-glycoprotein substrate + 0.5175 51.75%
CYP3A4 substrate + 0.6712 67.12%
CYP2C9 substrate - 0.6145 61.45%
CYP2D6 substrate + 0.3619 36.19%
CYP3A4 inhibition - 0.5469 54.69%
CYP2C9 inhibition + 0.8887 88.87%
CYP2C19 inhibition + 0.8894 88.94%
CYP2D6 inhibition - 0.8429 84.29%
CYP1A2 inhibition + 0.9253 92.53%
CYP2C8 inhibition + 0.7666 76.66%
CYP inhibitory promiscuity + 0.8164 81.64%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.6167 61.67%
Carcinogenicity (trinary) Non-required 0.4496 44.96%
Eye corrosion - 0.9745 97.45%
Eye irritation - 0.8695 86.95%
Skin irritation - 0.6481 64.81%
Skin corrosion - 0.9260 92.60%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8169 81.69%
Micronuclear - 0.6000 60.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.7792 77.92%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity - 0.5625 56.25%
Nephrotoxicity - 0.5748 57.48%
Acute Oral Toxicity (c) III 0.5756 57.56%
Estrogen receptor binding + 0.8928 89.28%
Androgen receptor binding + 0.9184 91.84%
Thyroid receptor binding + 0.7767 77.67%
Glucocorticoid receptor binding + 0.8867 88.67%
Aromatase binding + 0.6172 61.72%
PPAR gamma + 0.8793 87.93%
Honey bee toxicity - 0.8934 89.34%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.6152 61.52%
Fish aquatic toxicity + 0.9918 99.18%

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
CHEMBL1951 P21397 Monoamine oxidase A 99.14% 91.49%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.71% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.81% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.07% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.56% 86.33%
CHEMBL4208 P20618 Proteasome component C5 91.00% 90.00%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 90.89% 89.62%
CHEMBL2056 P21728 Dopamine D1 receptor 89.90% 91.00%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 89.72% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.00% 95.56%
CHEMBL2535 P11166 Glucose transporter 88.82% 98.75%
CHEMBL3194 P02766 Transthyretin 88.46% 90.71%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.36% 99.15%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 85.64% 95.34%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.63% 95.89%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 85.29% 98.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.98% 94.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 84.48% 90.24%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.35% 94.45%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 82.49% 95.78%
CHEMBL5905 Q04828 Aldo-keto reductase family 1 member C1 81.86% 91.79%
CHEMBL5311 P37023 Serine/threonine-protein kinase receptor R3 81.47% 82.67%

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.
Lepidozia incurvata

Cross-Links

Top
PubChem 101263411
LOTUS LTS0231091
wikiData Q105348672