Cassiaside

Details

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Internal ID 5d045f4a-dfe2-4cca-8d7a-af953b1d7567
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones > Naphthopyranone glycosides
IUPAC Name 5-hydroxy-2-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzo[g]chromen-4-one
SMILES (Canonical) CC1=CC(=O)C2=C(O1)C=C3C=CC=C(C3=C2O)OC4C(C(C(C(O4)CO)O)O)O
SMILES (Isomeric) CC1=CC(=O)C2=C(O1)C=C3C=CC=C(C3=C2O)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O
InChI InChI=1S/C20H20O9/c1-8-5-10(22)15-12(27-8)6-9-3-2-4-11(14(9)17(15)24)28-20-19(26)18(25)16(23)13(7-21)29-20/h2-6,13,16,18-21,23-26H,7H2,1H3/t13-,16-,18+,19-,20-/m1/s1
InChI Key SBVZTBIAKFTNIJ-CZNQJBLBSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C20H20O9
Molecular Weight 404.40 g/mol
Exact Mass 404.11073221 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.14
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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123914-49-8
13709-03-0
Cassiaside A
5-hydroxy-2-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzo[g]chromen-4-one
4H-Naphtho(2,3-b)pyran-4-one, 6-(beta-D-glucopyranosyloxy)-5-hydroxy-2-methyl-
DTXSID70154145
CHEBI:168433
C20-H29-O9
E87130
4H-Naphtho[2,3-b]pyran-4-one,6-(beta-D-glucopyranosyloxy)-5-hydroxy-2-methyl-

2D Structure

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2D Structure of Cassiaside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5998 59.98%
Caco-2 - 0.8540 85.40%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6483 64.83%
OATP2B1 inhibitior - 0.5499 54.99%
OATP1B1 inhibitior + 0.8945 89.45%
OATP1B3 inhibitior + 0.9671 96.71%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6848 68.48%
P-glycoprotein inhibitior - 0.8091 80.91%
P-glycoprotein substrate - 0.8024 80.24%
CYP3A4 substrate + 0.6087 60.87%
CYP2C9 substrate - 0.6986 69.86%
CYP2D6 substrate - 0.8617 86.17%
CYP3A4 inhibition - 0.9417 94.17%
CYP2C9 inhibition - 0.9552 95.52%
CYP2C19 inhibition - 0.9427 94.27%
CYP2D6 inhibition - 0.9493 94.93%
CYP1A2 inhibition - 0.9020 90.20%
CYP2C8 inhibition - 0.6294 62.94%
CYP inhibitory promiscuity - 0.8183 81.83%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6495 64.95%
Eye corrosion - 0.9920 99.20%
Eye irritation - 0.8969 89.69%
Skin irritation - 0.8214 82.14%
Skin corrosion - 0.9690 96.90%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4905 49.05%
Micronuclear + 0.5633 56.33%
Hepatotoxicity - 0.7199 71.99%
skin sensitisation - 0.9235 92.35%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6634 66.34%
Acute Oral Toxicity (c) III 0.6607 66.07%
Estrogen receptor binding + 0.7614 76.14%
Androgen receptor binding + 0.5959 59.59%
Thyroid receptor binding + 0.5284 52.84%
Glucocorticoid receptor binding + 0.7457 74.57%
Aromatase binding + 0.6894 68.94%
PPAR gamma + 0.6488 64.88%
Honey bee toxicity - 0.8444 84.44%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7150 71.50%
Fish aquatic toxicity + 0.7355 73.55%

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 98.42% 91.11%
CHEMBL220 P22303 Acetylcholinesterase 98.01% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.33% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 96.27% 94.73%
CHEMBL2581 P07339 Cathepsin D 95.91% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.84% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.34% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.25% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.62% 99.17%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.90% 99.23%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 83.69% 96.21%
CHEMBL1951 P21397 Monoamine oxidase A 81.96% 91.49%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.32% 90.71%

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.
Erythrophleum ivorense
Senna obtusifolia
Senna tora

Cross-Links

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PubChem 164146
NPASS NPC676
LOTUS LTS0122589
wikiData Q72515848