Rubrofusarin-6-glucoside

Details

Top
Internal ID a9e89fe9-23a6-4a31-9c73-cd7b79070d4f
Taxonomy Organoheterocyclic compounds > Naphthopyrans > Naphthopyranones > Naphthopyranone glycosides
IUPAC Name 5-hydroxy-8-methoxy-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(C3=C(C=C(C=C3C=C2O1)OC)OC4C(C(C(C(O4)CO)O)O)O)O
SMILES (Isomeric) CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2O1)OC)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)O
InChI InChI=1S/C21H22O10/c1-8-3-11(23)16-12(29-8)5-9-4-10(28-2)6-13(15(9)18(16)25)30-21-20(27)19(26)17(24)14(7-22)31-21/h3-6,14,17,19-22,24-27H,7H2,1-2H3/t14-,17-,19+,20-,21-/m1/s1
InChI Key CDMUGCVTTUOCFT-IAAKTDFRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C21H22O10
Molecular Weight 434.40 g/mol
Exact Mass 434.12129689 g/mol
Topological Polar Surface Area (TPSA) 155.00 Ų
XlogP 1.20
Atomic LogP (AlogP) 0.15
H-Bond Acceptor 10
H-Bond Donor 5
Rotatable Bonds 4

Synonyms

Top
132922-80-6
6-(beta-D-Glucopyranosyloxy)-5-hydroxy-8-methoxy-2-methyl-4H-naphtho(2,3-b)pyran-4-one
5-hydroxy-8-methoxy-2-methyl-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybenzo[g]chromen-4-one
CHEMBL3634698
DTXSID10157857
E89052
RUBROFUSARIN-6-O-BETA-D-GLUCOPYRANOSIDE
2-Methyl-5-hydroxy-6-(beta-D-glucopyranosyloxy)-8-methoxy-4H-naphtho[2,3-b]pyran-4-one
4H-Naphtho(2,3-b)pyran-4-one, 6-(beta-D-glucopyranosyloxy)-5-hydroxy-8-methoxy-2-methyl-

2D Structure

Top
2D Structure of Rubrofusarin-6-glucoside

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6307 63.07%
Caco-2 - 0.7987 79.87%
Blood Brain Barrier - 0.8000 80.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.5843 58.43%
OATP2B1 inhibitior - 0.5545 55.45%
OATP1B1 inhibitior + 0.8657 86.57%
OATP1B3 inhibitior + 0.9664 96.64%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.5215 52.15%
P-glycoprotein inhibitior - 0.7203 72.03%
P-glycoprotein substrate - 0.7521 75.21%
CYP3A4 substrate + 0.5976 59.76%
CYP2C9 substrate - 0.8740 87.40%
CYP2D6 substrate - 0.8547 85.47%
CYP3A4 inhibition - 0.8955 89.55%
CYP2C9 inhibition - 0.9543 95.43%
CYP2C19 inhibition - 0.9390 93.90%
CYP2D6 inhibition - 0.9142 91.42%
CYP1A2 inhibition - 0.9202 92.02%
CYP2C8 inhibition - 0.6537 65.37%
CYP inhibitory promiscuity - 0.8251 82.51%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6850 68.50%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9143 91.43%
Skin irritation - 0.8318 83.18%
Skin corrosion - 0.9683 96.83%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3827 38.27%
Micronuclear + 0.5933 59.33%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.9297 92.97%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity - 0.7636 76.36%
Acute Oral Toxicity (c) III 0.7389 73.89%
Estrogen receptor binding + 0.7946 79.46%
Androgen receptor binding + 0.6070 60.70%
Thyroid receptor binding + 0.5897 58.97%
Glucocorticoid receptor binding + 0.7902 79.02%
Aromatase binding + 0.6941 69.41%
PPAR gamma + 0.6653 66.53%
Honey bee toxicity - 0.8210 82.10%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7800 78.00%
Fish aquatic toxicity - 0.3644 36.44%

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 99.02% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.49% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 96.47% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 94.90% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.29% 95.56%
CHEMBL2581 P07339 Cathepsin D 89.67% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.18% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.87% 86.92%
CHEMBL3714130 P46095 G-protein coupled receptor 6 88.66% 97.36%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.59% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.55% 89.00%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 85.91% 99.15%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.45% 96.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.69% 96.21%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.50% 99.23%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.43% 94.42%
CHEMBL4581 P52732 Kinesin-like protein 1 80.04% 93.18%

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.
Senna obtusifolia
Senna tora

Cross-Links

Top
PubChem 3035617
NPASS NPC259905
LOTUS LTS0040724
wikiData Q83026023