Cleistanthoside A

Details

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Internal ID d4f07dd0-eb5b-4f9f-a966-916d2d1257f5
Taxonomy Lignans, neolignans and related compounds > Lignan glycosides
IUPAC Name 9-(1,3-benzodioxol-5-yl)-4-[(2S,3R,4S,5R)-4,5-dimethoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one
SMILES (Canonical) COC1COC(C(C1OC)OC2C(C(C(C(O2)CO)O)O)O)OC3=C4COC(=O)C4=C(C5=CC(=C(C=C53)OC)OC)C6=CC7=C(C=C6)OCO7
SMILES (Isomeric) CO[C@@H]1CO[C@H]([C@@H]([C@H]1OC)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)OC3=C4COC(=O)C4=C(C5=CC(=C(C=C53)OC)OC)C6=CC7=C(C=C6)OCO7
InChI InChI=1S/C34H38O16/c1-40-19-8-15-16(9-20(19)41-2)29(17-11-44-32(39)25(17)24(15)14-5-6-18-21(7-14)47-13-46-18)49-34-31(30(43-4)23(42-3)12-45-34)50-33-28(38)27(37)26(36)22(10-35)48-33/h5-9,22-23,26-28,30-31,33-38H,10-13H2,1-4H3/t22-,23-,26-,27+,28-,30+,31-,33+,34+/m1/s1
InChI Key JBVKVMLXAUHJEJ-LXOHQACASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C34H38O16
Molecular Weight 702.70 g/mol
Exact Mass 702.21598512 g/mol
Topological Polar Surface Area (TPSA) 200.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 0.87
H-Bond Acceptor 16
H-Bond Donor 4
Rotatable Bonds 10

Synonyms

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86402-39-3
CHEMBL3298958
DTXSID90235526
Naphtho(2,3-c)furan-1(3H)-one, 9-(1,3-benzodioxol-5-yl)-4-((2-O-beta-D-glucopyranosyl-3,4-di-O-methyl-beta-D-xylopyranosyl)oxy)-6,7-dimethoxy-

2D Structure

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2D Structure of Cleistanthoside A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6717 67.17%
Caco-2 - 0.8344 83.44%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.5839 58.39%
OATP2B1 inhibitior - 0.8626 86.26%
OATP1B1 inhibitior + 0.8683 86.83%
OATP1B3 inhibitior + 0.9574 95.74%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9680 96.80%
P-glycoprotein inhibitior + 0.6634 66.34%
P-glycoprotein substrate + 0.5437 54.37%
CYP3A4 substrate + 0.6934 69.34%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8533 85.33%
CYP3A4 inhibition - 0.7416 74.16%
CYP2C9 inhibition - 0.8441 84.41%
CYP2C19 inhibition - 0.8222 82.22%
CYP2D6 inhibition - 0.9268 92.68%
CYP1A2 inhibition - 0.9014 90.14%
CYP2C8 inhibition + 0.6661 66.61%
CYP inhibitory promiscuity + 0.5153 51.53%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6315 63.15%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.9387 93.87%
Skin irritation - 0.8131 81.31%
Skin corrosion - 0.9476 94.76%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8045 80.45%
Micronuclear + 0.5300 53.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.8878 88.78%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7956 79.56%
Acute Oral Toxicity (c) III 0.6553 65.53%
Estrogen receptor binding + 0.8204 82.04%
Androgen receptor binding + 0.6464 64.64%
Thyroid receptor binding + 0.5221 52.21%
Glucocorticoid receptor binding + 0.7068 70.68%
Aromatase binding - 0.4854 48.54%
PPAR gamma + 0.7003 70.03%
Honey bee toxicity - 0.6486 64.86%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.8696 86.96%

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 99.24% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.77% 94.45%
CHEMBL2581 P07339 Cathepsin D 96.76% 98.95%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 96.09% 96.77%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 95.59% 94.80%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.97% 89.00%
CHEMBL1951 P21397 Monoamine oxidase A 94.71% 91.49%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 94.53% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.52% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.92% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.42% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.17% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.68% 94.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.72% 97.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.38% 99.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.68% 96.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 85.98% 97.28%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.45% 100.00%
CHEMBL5555 O00767 Acyl-CoA desaturase 83.16% 97.50%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 82.70% 97.14%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 82.26% 96.21%
CHEMBL2535 P11166 Glucose transporter 81.65% 98.75%

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.
Cleistanthus patulus
Phyllanthus taxodiifolius

Cross-Links

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PubChem 158941
LOTUS LTS0238175
wikiData Q83117409