Saikochromoside A

Details

Top
Internal ID a45d7318-3d62-4045-a860-d4cf5c49fc0b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name 5-hydroxy-7-methoxy-2-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]chromen-4-one
SMILES (Canonical) COC1=CC(=C2C(=C1)OC(=CC2=O)COC3C(C(C(C(O3)CO)O)O)O)O
SMILES (Isomeric) COC1=CC(=C2C(=C1)OC(=CC2=O)CO[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O
InChI InChI=1S/C17H20O10/c1-24-7-2-9(19)13-10(20)3-8(26-11(13)4-7)6-25-17-16(23)15(22)14(21)12(5-18)27-17/h2-4,12,14-19,21-23H,5-6H2,1H3/t12-,14-,15+,16-,17-/m1/s1
InChI Key UIKLIOIWCUSJML-USACIQFYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C17H20O10
Molecular Weight 384.30 g/mol
Exact Mass 384.10564683 g/mol
Topological Polar Surface Area (TPSA) 155.00 Ų
XlogP -0.80
Atomic LogP (AlogP) -1.18
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

Top
CHEMBL2087916

2D Structure

Top
2D Structure of Saikochromoside A

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6786 67.86%
Caco-2 - 0.7353 73.53%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.8143 81.43%
Subcellular localzation Mitochondria 0.5623 56.23%
OATP2B1 inhibitior - 0.5701 57.01%
OATP1B1 inhibitior + 0.8954 89.54%
OATP1B3 inhibitior + 0.9803 98.03%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.6320 63.20%
P-glycoprotein inhibitior - 0.8179 81.79%
P-glycoprotein substrate - 0.8336 83.36%
CYP3A4 substrate + 0.5488 54.88%
CYP2C9 substrate - 0.8485 84.85%
CYP2D6 substrate - 0.8501 85.01%
CYP3A4 inhibition - 0.9532 95.32%
CYP2C9 inhibition - 0.9448 94.48%
CYP2C19 inhibition - 0.9062 90.62%
CYP2D6 inhibition - 0.9288 92.88%
CYP1A2 inhibition - 0.9189 91.89%
CYP2C8 inhibition - 0.6596 65.96%
CYP inhibitory promiscuity - 0.8207 82.07%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6080 60.80%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9473 94.73%
Skin irritation - 0.8346 83.46%
Skin corrosion - 0.9670 96.70%
Ames mutagenesis + 0.6463 64.63%
Human Ether-a-go-go-Related Gene inhibition - 0.8098 80.98%
Micronuclear + 0.5633 56.33%
Hepatotoxicity - 0.9125 91.25%
skin sensitisation - 0.9248 92.48%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.7968 79.68%
Acute Oral Toxicity (c) III 0.7273 72.73%
Estrogen receptor binding + 0.7532 75.32%
Androgen receptor binding + 0.6727 67.27%
Thyroid receptor binding + 0.5661 56.61%
Glucocorticoid receptor binding + 0.6034 60.34%
Aromatase binding + 0.6479 64.79%
PPAR gamma + 0.5884 58.84%
Honey bee toxicity - 0.8032 80.32%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.4641 46.41%

Targets

Top

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 99.45% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 95.96% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.42% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.48% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 91.13% 94.73%
CHEMBL2581 P07339 Cathepsin D 90.61% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.46% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 89.32% 99.15%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.62% 89.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.62% 96.09%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 86.07% 86.92%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.53% 97.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.27% 97.36%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.60% 86.33%
CHEMBL3194 P02766 Transthyretin 82.50% 90.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.09% 94.45%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 80.40% 96.21%

Plants that contains it

Top
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.
Bupleurum chinense
Cnidium monnieri

Cross-Links

Top
PubChem 70697379
NPASS NPC207894
LOTUS LTS0046871
wikiData Q105273415