Rutoside
C05C - Capillary stabilizing agents
ATC C05CA01
Small molecule
Natural product
JFDA label: VENORUTON FORTE TAB
Indications
Off-label
- Cardiovascular Diseases
- Prostatic Neoplasms, Castration-Resistant
- Venous Thrombosis
Chemistry & Properties
| Formula | C27H30O16 |
|---|---|
| Molecular weight | 610.52 g/mol |
| IUPAC name | 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one |
| CAS | 153-18-4 |
| PubChem CID | 5280805 |
| InChIKey | IKGXIBQEEMLURG-NVPNHPEKSA-N |
| logP | -1.69 (XLogP -1.3) |
| Polar surface area | 269.43 Ų |
| H-bond acceptors / donors | 16 / 10 |
| Drug-likeness (QED) | 0.14 |
| Lipinski violations | 3 |
SMILES
C[C@@H]1O[C@@H](OC[C@H]2O[C@@H](Oc3c(-c4ccc(O)c(O)c4)oc4cc(O)cc(O)c4c3=O)[C@H](O)[C@@H](O)[C@@H]2O)[C@H](O)[C@H](O)[C@H]1OBiology & Pharmacokinetics
Pharmacokinetics predicted
| Bioavailability | 70.0% |
|---|---|
| Half-life | 4.616 h |
| Volume of distribution | 0.873 L/kg |
| Protein binding | 85.0% |
| BBB penetrant | No |
Enzyme interactions
| Enzyme | Role | Detail |
|---|---|---|
| CYP2C8 | Inhibitor | — |
Transporters
BCRP (Inhibitor)BSEP (Inhibitor)MRP1 (Inhibitor)OATP1B1 (Inhibitor)OATP1B3 (Inhibitor)P-gp (Inhibitor)P-gp (Substrate)
Registered Products (2)
| Brand | Form / strength | Pack | Agent | Citizen (JOD) |
|---|---|---|---|---|
| Pharmaton Capsules | Capsule 20 mg, 15 mg, 10 mg, 60 mg, 400 IU, 2 mg, 4000 IU, 1 mcg, 90.3 mg, 1 mg, 10 mg, 1 mg, 10 mg, 40 mg, 10 mg, 1 mg, 2 mg, 8 mg, 66 mg, 1 mg, 26 mg, 70 mg, 0.2 mg | 30 cap | THE ARAB DRUG STORE P.S.C | 6.700 |
| VENORUTON FORTE TAB | Tablet 500 mg | 30 tab | Nabulsi Drug Store | 8.280 |