CID 53473939

Details

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Internal ID 91f411f5-ef29-4e3d-a728-3fa9eeaff408
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name (19R,21R,22S)-8-chloro-3,10,19,21,22,26-hexahydroxy-15-methoxy-6-methyl-7-propyl-17-oxa-6-azahexacyclo[12.12.0.02,11.04,9.016,25.018,23]hexacosa-1(14),2(11),3,7,9,15,18(23),25-octaene-5,24-dione
SMILES (Canonical) CCCC1=C(C2=C(C3=C(C4=C(CC3)C(=C5C(=C4O)C(=O)C6=C(O5)C(CC(C6O)O)O)OC)C(=C2C(=O)N1C)O)O)Cl
SMILES (Isomeric) CCCC1=C(C2=C(C3=C(C4=C(CC3)C(=C5C(=C4O)C(=O)C6=C(O5)[C@@H](C[C@H]([C@H]6O)O)O)OC)C(=C2C(=O)N1C)O)O)Cl
InChI InChI=1S/C29H28ClNO10/c1-4-5-11-20(30)16-17(29(39)31(11)2)23(36)14-9(21(16)34)6-7-10-15(14)24(37)19-25(38)18-22(35)12(32)8-13(33)27(18)41-28(19)26(10)40-3/h12-13,22,32-37H,4-8H2,1-3H3/t12-,13-,22-/m1/s1
InChI Key NEZGGHIIKFHZCZ-GIYNXVAASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C29H28ClNO10
Molecular Weight 586.00 g/mol
Exact Mass 585.1401738 g/mol
Topological Polar Surface Area (TPSA) 177.00 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.97
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 53473939

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8034 80.34%
Caco-2 - 0.8055 80.55%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Lysosomes 0.3870 38.70%
OATP2B1 inhibitior - 0.7195 71.95%
OATP1B1 inhibitior + 0.8298 82.98%
OATP1B3 inhibitior + 0.9242 92.42%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.7572 75.72%
BSEP inhibitior - 0.5783 57.83%
P-glycoprotein inhibitior - 0.4644 46.44%
P-glycoprotein substrate + 0.6410 64.10%
CYP3A4 substrate + 0.7136 71.36%
CYP2C9 substrate - 0.5835 58.35%
CYP2D6 substrate - 0.8438 84.38%
CYP3A4 inhibition - 0.6876 68.76%
CYP2C9 inhibition - 0.7911 79.11%
CYP2C19 inhibition - 0.7540 75.40%
CYP2D6 inhibition - 0.8657 86.57%
CYP1A2 inhibition - 0.6674 66.74%
CYP2C8 inhibition + 0.6984 69.84%
CYP inhibitory promiscuity - 0.7156 71.56%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Non-required 0.4415 44.15%
Eye corrosion - 0.9860 98.60%
Eye irritation - 0.9298 92.98%
Skin irritation - 0.7887 78.87%
Skin corrosion - 0.9295 92.95%
Ames mutagenesis - 0.5254 52.54%
Human Ether-a-go-go-Related Gene inhibition - 0.4519 45.19%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.6053 60.53%
skin sensitisation - 0.8711 87.11%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.9000 90.00%
Nephrotoxicity - 0.7699 76.99%
Acute Oral Toxicity (c) III 0.5778 57.78%
Estrogen receptor binding + 0.7850 78.50%
Androgen receptor binding + 0.6552 65.52%
Thyroid receptor binding + 0.5715 57.15%
Glucocorticoid receptor binding + 0.7199 71.99%
Aromatase binding + 0.6906 69.06%
PPAR gamma + 0.6292 62.92%
Honey bee toxicity - 0.7852 78.52%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.8135 81.35%

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
CHEMBL2581 P07339 Cathepsin D 96.76% 98.95%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 96.10% 95.34%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 95.94% 94.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.45% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.16% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 93.59% 96.77%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.82% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.72% 91.11%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 89.51% 92.62%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.16% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.81% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.45% 86.33%
CHEMBL5905 Q04828 Aldo-keto reductase family 1 member C1 86.99% 91.79%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 85.49% 100.00%
CHEMBL1871 P10275 Androgen Receptor 85.39% 96.43%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 85.29% 86.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.05% 95.89%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 84.58% 95.17%
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 84.04% 92.38%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.46% 90.71%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 80.80% 92.68%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.28% 94.42%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 53473939
LOTUS LTS0094611
wikiData Q58049418