Lespecyrtin H2

Details

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Internal ID 024872c9-4b0e-43b8-a151-dccda02a6472
Taxonomy Phenylpropanoids and polyketides > 2-arylbenzofuran flavonoids
IUPAC Name (6bR,10aS)-8-[2-[2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,6-dihydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-3-carbonyl]-3,9-dihydroxy-2,10-bis(3-methylbut-2-enyl)-6b,10a-dihydro-[1]benzofuro[3,2-c]chromen-6-one
SMILES (Canonical) CC(=CCC1=CC(=C(C=C1O)O)C2=C(C3=CC(=C(C(=C3O2)CC=C(C)C)O)O)C(=O)C4=CC5C(C(=C4O)CC=C(C)C)OC6=C5C(=O)OC7=C6C=C(C(=C7)O)CC=C(C)C)C
SMILES (Isomeric) CC(=CCC1=CC(=C(C=C1O)O)C2=C(C3=CC(=C(C(=C3O2)CC=C(C)C)O)O)C(=O)C4=C[C@H]5[C@@H](C(=C4O)CC=C(C)C)OC6=C5C(=O)OC7=C6C=C(C(=C7)O)CC=C(C)C)C
InChI InChI=1S/C50H50O11/c1-23(2)9-13-27-17-31(38(53)21-36(27)51)48-41(34-20-39(54)44(56)30(47(34)60-48)16-12-26(7)8)45(57)35-19-33-42-49(61-46(33)29(43(35)55)15-11-25(5)6)32-18-28(14-10-24(3)4)37(52)22-40(32)59-50(42)58/h9-12,17-22,33,46,51-56H,13-16H2,1-8H3/t33-,46-/m1/s1
InChI Key RXYKSFVXSAQWGF-XGLXXXPISA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C50H50O11
Molecular Weight 826.90 g/mol
Exact Mass 826.33531241 g/mol
Topological Polar Surface Area (TPSA) 187.00 Ų
XlogP 11.20
Atomic LogP (AlogP) 11.10
H-Bond Acceptor 11
H-Bond Donor 6
Rotatable Bonds 11

Synonyms

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CHEMBL538958

2D Structure

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2D Structure of Lespecyrtin H2

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9258 92.58%
Caco-2 - 0.8670 86.70%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6921 69.21%
OATP2B1 inhibitior + 0.5780 57.80%
OATP1B1 inhibitior + 0.8364 83.64%
OATP1B3 inhibitior + 0.9311 93.11%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.8815 88.15%
P-glycoprotein inhibitior + 0.7873 78.73%
P-glycoprotein substrate + 0.7602 76.02%
CYP3A4 substrate + 0.6707 67.07%
CYP2C9 substrate + 0.6397 63.97%
CYP2D6 substrate - 0.8692 86.92%
CYP3A4 inhibition - 0.8214 82.14%
CYP2C9 inhibition + 0.8121 81.21%
CYP2C19 inhibition + 0.6475 64.75%
CYP2D6 inhibition - 0.8338 83.38%
CYP1A2 inhibition - 0.6187 61.87%
CYP2C8 inhibition + 0.6556 65.56%
CYP inhibitory promiscuity + 0.6541 65.41%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.4988 49.88%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9062 90.62%
Skin irritation - 0.7184 71.84%
Skin corrosion - 0.9223 92.23%
Ames mutagenesis + 0.5963 59.63%
Human Ether-a-go-go-Related Gene inhibition + 0.8094 80.94%
Micronuclear + 0.5800 58.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.8024 80.24%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.8621 86.21%
Acute Oral Toxicity (c) III 0.4329 43.29%
Estrogen receptor binding + 0.8086 80.86%
Androgen receptor binding + 0.7893 78.93%
Thyroid receptor binding + 0.5915 59.15%
Glucocorticoid receptor binding + 0.7457 74.57%
Aromatase binding + 0.5800 58.00%
PPAR gamma + 0.7370 73.70%
Honey bee toxicity - 0.7643 76.43%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 1.0000 100.00%

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 99.86% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.00% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 93.63% 94.73%
CHEMBL2581 P07339 Cathepsin D 92.71% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 92.01% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.17% 95.56%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.91% 92.62%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 87.69% 95.58%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.36% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.40% 94.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.03% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.95% 99.17%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.66% 91.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.12% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.79% 100.00%

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.
Lespedeza cyrtobotrya

Cross-Links

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PubChem 45273188
LOTUS LTS0089222
wikiData Q105247374