Hastatuside A

Details

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Internal ID 3292f660-64ad-499d-b82a-199efe2800e9
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Coumarin glycosides
IUPAC Name 7-hydroxy-5-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one
SMILES (Canonical) CC1=CC(=CC2=C1C(=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)O
SMILES (Isomeric) CC1=CC(=CC2=C1C(=CC(=O)O2)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O
InChI InChI=1S/C16H18O9/c1-6-2-7(18)3-8-12(6)9(4-11(19)23-8)24-16-15(22)14(21)13(20)10(5-17)25-16/h2-4,10,13-18,20-22H,5H2,1H3/t10-,13-,14+,15-,16-/m1/s1
InChI Key NPDJLYQZNREONG-LMXXTMHSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H18O9
Molecular Weight 354.31 g/mol
Exact Mass 354.09508215 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP -0.50
Atomic LogP (AlogP) -1.01
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hastatuside A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5998 59.98%
Caco-2 - 0.7746 77.46%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6483 64.83%
OATP2B1 inhibitior - 0.7108 71.08%
OATP1B1 inhibitior + 0.9028 90.28%
OATP1B3 inhibitior + 0.9671 96.71%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9185 91.85%
P-glycoprotein inhibitior - 0.9081 90.81%
P-glycoprotein substrate - 0.8644 86.44%
CYP3A4 substrate + 0.5312 53.12%
CYP2C9 substrate - 0.8173 81.73%
CYP2D6 substrate - 0.8664 86.64%
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 - 0.6489 64.89%
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 - 0.8962 89.62%
Skin irritation - 0.8214 82.14%
Skin corrosion - 0.9690 96.90%
Ames mutagenesis - 0.5754 57.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5073 50.73%
Micronuclear + 0.5633 56.33%
Hepatotoxicity - 0.7423 74.23%
skin sensitisation - 0.9235 92.35%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6411 64.11%
Acute Oral Toxicity (c) III 0.6607 66.07%
Estrogen receptor binding + 0.6062 60.62%
Androgen receptor binding + 0.6028 60.28%
Thyroid receptor binding - 0.5551 55.51%
Glucocorticoid receptor binding + 0.7355 73.55%
Aromatase binding + 0.5207 52.07%
PPAR gamma + 0.5604 56.04%
Honey bee toxicity - 0.7721 77.21%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6400 64.00%
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 98.40% 91.11%
CHEMBL220 P22303 Acetylcholinesterase 97.71% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.17% 94.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 94.14% 96.21%
CHEMBL3401 O75469 Pregnane X receptor 93.82% 94.73%
CHEMBL2581 P07339 Cathepsin D 93.05% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.55% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.46% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.81% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.96% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.46% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.22% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 83.08% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.11% 99.23%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.08% 93.65%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 80.73% 83.57%
CHEMBL3194 P02766 Transthyretin 80.55% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.38% 96.95%

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.
Rumex hastatus

Cross-Links

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PubChem 102480464
LOTUS LTS0050701
wikiData Q105182983