Page last updated: 2024-11-11

troxerutin

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Description

troxerutin: used in treatment of venous disorders; structure; venoruton & oxerutin is a mixture of hydroxyethyl rutinosides [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5486699
CHEMBL ID3182320
SCHEMBL ID142110
MeSH IDM0047701

Synonyms (99)

Synonym
flebil
tris(hydroxyethyl)rutin
troxarutin-ratiopharm
troxerutina [inn-spanish]
helveton
2-(3,4-bis(2-hydroxyethoxy)phenyl)-3-((6-o-(6-deoxy-alpha-l-mannopyranosyl)-beta-d-glucopyranosyl)oxy)-5-hydroxy-7-(2-hydroxy ethoxy)-4h-1-benzopyran-4-one
troxerutine [inn-french]
troxarutin
troxerutinum [inn-latin]
venaroid
flavone, 3,5-dihydroxy-3',4',7-tris(2-hydroxyethoxy)-, 3-(6-o-(6-deoxy-alpha-l-mannopyranosyl)-beta-d-glucopyranoside)
troxerutin [inn:ban:dcf]
factor p-zyma
3',4',7-tris(hydroxyethyl)rutin
trihydroxyethylrutoside [french]
ccris 1798
veinamitol pulver
troksevazin
tris(hydroxyethyl)rutoside
venoruton p4
pur-rutin
z 6000
rufen-p4
7,3',4'-tris(o-(2-hydroxyethyl)rutin
posorutin
einecs 230-389-4
vitamin p4
veno sl
pherarutin
brn 4778232
troxerutin
D07180
7085-55-4
troxerutin (inn)
NCGC00095147-01
vastribil
veinamitol
trihydroxyethylrutin, >=80% (hplc)
2-[3,4-bis(2-hydroxyethoxy)phenyl]-5-hydroxy-7-(2-hydroxyethoxy)-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
A837010
2-[3,4-bis(2-hydroxyethyloxy)phenyl]-7-(2-hydroxyethyloxy)-3-[(2s,3r,4s,5s,6r)-6-[[(2r,3r,4r,5r,6s)-6-methyl-3,4,5-tris(oxidanyl)oxan-2-yl]oxymethyl]-3,4,5-tris(oxidanyl)oxan-2-yl]oxy-5-oxidanyl-chromen-4-one
2-[3,4-bis(2-hydroxyethoxy)phenyl]-5-hydroxy-7-(2-hydroxyethoxy)-3-[[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-[[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyl-2-oxanyl]oxymethyl]-2-oxanyl]oxy]-1-benzopyran-4-one
808o347b5y ,
unii-808o347b5y
55965-63-4
venoruton gel
nsc-758937
tox21_111450
cas-7085-55-4
dtxsid4045929 ,
dtxcid2025929
nsc 758937
7y4n11pxo8 ,
troxerutine
trihydroxyethylrutoside
troxerutina
unii-7y4n11pxo8
troxerutinum
trihydroxyethylrutin
AKOS016339659
veniten
ruven
trioxyethylrutin
4h-1-benzopyran-4-one, 2-(3,4-bis(2-hydroxyethoxy)phenyl)-3-((6-o-(6-deoxy-.alpha.-l-mannopyranosyl)-.beta.-d-glucopyranosyl)oxy)-5-hydroxy-7-(2-hydroxyethoxy)-
troxerutin [inci]
troxerutin [who-dd]
troxerutin [ep monograph]
o-(.beta.-hydroxyethyl)rutoside, (3',4',7)-tri-
troxerutin [mart.]
troxerutin [mi]
z-6000 ,
troxerutin [inn]
SCHEMBL142110
KS-1394
succinimidyln-methylanthranilate
S2369
IYVFNTXFRYQLRP-VVSTWUKXSA-N
3,5-dihydroxy-3',4',7-tris(2-hydroxyethoxy)flavone 3-rutinoside
4h-1-benzopyran-4-one, 2-[3,4-bis(2-hydroxyethoxy)phenyl]-3-[[6-o-(6-deoxy-.alpha.-l-mannopyranosyl)-.beta.-d-glucopyranosyl]oxy]-5-hydroxy-7-(2-hydroxyethoxy)-
CHEMBL3182320
2-[3,4-bis(2-hydroxyethoxy)phenyl]-5-hydroxy-7-(2-hydroxyethoxy)-3-{[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-({[(2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}methyl)oxan-2-yl]oxy}-4h-chromen-4-one
2-(3,4-bis(2-hydroxyethoxy)phenyl)-5-hydroxy-7-(2-hydroxyethoxy)-3-(((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-((((2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyltetrahydro-2h-pyran-2-yl)oxy)methyl)tetrahydro-2h-pyran-2-yl)oxy)-4h-chromen-4-one
tris-o-(2-hydroxyethyl)rutin
triher
tris-o-(b-hydroxyethyl)rutoside
3-[6-o-(6-deoxy-alpha-l-mannopyranosyl)-beta-delta-glucopyranoside]3,5-dihydroxy-3',4',7-tris(2-hydroxyethoxy)-flavone
3',4',7-tri-o-(b-hydroxyethyl)rutoside
3-[6-o-(6-deoxy-a-l-mannopyranosyl)-b-d-glucopyranoside]3,5-dihydroxy-3',4',7-tris(2-hydroxyethoxy)-flavone
troxerutin, european pharmacopoeia (ep) reference standard
DB13124
CS-8204
2-(3,4-bis(2-hydroxyethoxy)phenyl)-5-hydroxy-7-(2-hydroxyethoxy)-3-((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(((2r,3r,4r,5r,6s)-3,4,5-trihydroxy-6-methyltetrahydro-2h-pyran-2-yloxy)methyl)tetrahydro-2h-pyran-2-yloxy)-4h-chromen-4-one
HY-N0139
mfcd00893813
troxerutin,(s)
BRD-K73529671-001-04-5
CCG-270428
4h-1-benzopyran-4-one,2-[3,4-bis(2-hydroxyethoxy)phenyl]-3-[[6-o-(6-deoxy-a-l-mannopyranosyl)-b-d-glucopyranosyl]oxy]-5-hydroxy-7-(2-hydroxyethoxy)-
troxerutin (85%)

Research Excerpts

Overview

Troxerutin (TRX) is a natural flavonoid present abundantly in tea, coffee, olives, wheat, and a variety of fruits and vegetables. It is a bioflavonoid, which can be used to treat venous disorders, thrombosis and cerebrovascular diseases.

ExcerptReferenceRelevance
"Troxerutin (TRX) is a water-soluble flavonoid which occurs commonly in the edible plants. "( Troxerutin flavonoid has neuroprotective properties and increases neurite outgrowth and migration of neural stem cells from the subventricular zone.
Masood, MI; Meiser, P; Naseem, M; Schäfer, KH; Weyland, M, 2020
)
3.44
"Troxerutin is a natural flavonoid present abundantly in tea, coffee, olives, wheat, and a variety of fruits and vegetables. "( Chemopreventive effect of troxerutin against hydrogen peroxide-induced oxidative stress in human leukocytes through modulation of glutathione-dependent enzymes.
Barreto, FS; Cavalcanti, BC; Ferreira, JRO; Magalhães, HIF; Moraes, MO; Neto, JBA; Nobre Júnior, HV; Ricardo, NMPS; Silva, AAS; Silva, CRD; Vieira, ÍGP, 2021
)
2.36
"Troxerutin is a bioflavonoid, which can be used to treat venous disorders, thrombosis and cerebrovascular diseases. "( Troxerutin protects against diabetic cardiomyopathy through NF‑κB/AKT/IRS1 in a rat model of type 2 diabetes.
Yu, Y; Zheng, G, 2017
)
3.34
"Troxerutin is a flavonoid with pharmacological activity of antioxidation and anti-inflammation."( Troxerutin Reduces Kidney Damage against BDE-47-Induced Apoptosis via Inhibiting NOX2 Activity and Increasing Nrf2 Activity.
Lu, J; Shan, Q; Zhang, Y; Zhang, Z; Zheng, G; Zheng, Y; Zhuang, J, 2017
)
2.62
"Troxerutin (TRX) is a mixture of semisynthetic hydroxyethylrutosides (Hers) arising from hydroxyethylation of rutin, a natural occurring flavonoid. "( Troxerutin, a mixture of O-hydroxyethyl derivatives of the natural flavonoid rutin: Chemical stability and analytical aspects.
Aprile, S; Bianchi, M; Canavesi, R; Del Grosso, E; Grosa, G, 2018
)
3.37
"Troxerutin (Tx) is a natural flavonoid, also called vitamin P4, which is widely present in plants consumed as part of our daily diet, such as cereals, various fruits and vegetables, tea, and coffee, and possesses various biological activities, especially an anti-inflammatory effect."( Troxerutin suppresses the inflammatory response in advanced glycation end-product-administered chondrocytes and attenuates mouse osteoarthritis development.
Chen, B; Chen, Y; Pan, X; Wang, X; Wang, Y; Xue, X; Zhan, J, 2019
)
2.68
"Troxerutin is a natural flavonoid rutin mainly found in extracts of Sophora japonica, and is a well-known antioxidant and anti-inflammatory compound used in experimental mouse models."( Troxerutin induces protective effects against ultraviolet B radiation through the alteration of microRNA expression in human HaCaT keratinocyte cells.
Ahn, KJ; An, IS; An, S; Bae, S; Cha, HJ; Hong, JT; Lee, GT; Lee, KK; Lee, KS, 2014
)
2.57
"Troxerutin is a trihydroxyethylated derivative of the flavonoid, rutin. "( Effect of troxerutin on insulin signaling molecules in the gastrocnemius muscle of high fat and sucrose-induced type-2 diabetic adult male rat.
Karundevi, B; Sampath, S, 2014
)
2.25
"Troxerutin (TXER) is a derivative of naturally occurring bioflavonoid rutin. "( Spectroscopic and molecular docking studies on the interaction of troxerutin with DNA.
Harikrishna, M; Lokeswara Rao, P; Mareeswaran, R; Ramamurthy, CH; Subastri, A; Sujatha, V; Suresh Kumar, M; Suyavaran, A; Thirunavukkarasu, C, 2015
)
2.1
"Troxerutin (TRX) is a flavonoid present in tea, coffee, cereal grains, various fruits and vegetables have been reported to exhibit radioprotective, antithrombotic, nephro and hepato-protective effects. "( Troxerutin, a plant flavonoid, protects cells against oxidative stress-induced cell death through radical scavenging mechanism.
Ghaskadbi, SS; Maurya, DK; Panat, NA; Sandur, SK, 2016
)
3.32
"Troxerutin is a natural bioflavonoid with nephro- and hepato-protective, antioxidant, and anti-inflammatory properties."( Troxerutin exerts neuroprotection in 6-hydroxydopamine lesion rat model of Parkinson's disease: Possible involvement of PI3K/ERβ signaling.
Baluchnejadmojarad, T; Jamali-Raeufy, N; Rabiee, N; Roghani, M; Zabihnejad, S, 2017
)
2.62
"Troxerutin is a naturally fluorescent flavonoid which has been known to improve subjective signs of patients with chronic venous insufficiency."( [Transport and localization of troxerutin in the venous wall].
Carlsson, K; Gerentes, I; Patwardhan, A; Poullain, JC, 1996
)
1.3

Effects

Troxerutin has attracted much attention owing to its favorable properties, including antihyperglycemic, anti-inflammatory, and antiapoptotic effects. It is currently used for the treatment of chronic varicosity.

ExcerptReferenceRelevance
"Troxerutin (TRX) has a beneficial effect on blood viscosity and platelet aggregation, and is currently used for the treatment of chronic varicosity. "( Beneficial effects of troxerutin on metabolic disorders in non-obese model of metabolic syndrome.
Hüttl, M; Kazdova, L; Malinska, H; Markova, I; Oliyarnyk, O; Poruba, M; Racova, Z; Vecera, R, 2019
)
2.27
"Troxerutin (TRX) has a beneficial effect on blood viscosity and platelet aggregation, and is currently used for the treatment of chronic varicosity. "( Beneficial effects of troxerutin on metabolic disorders in non-obese model of metabolic syndrome.
Hüttl, M; Kazdova, L; Malinska, H; Markova, I; Oliyarnyk, O; Poruba, M; Racova, Z; Vecera, R, 2019
)
2.27
"Troxerutin has attracted much attention owing to its favorable properties, including antihyperglycemic, anti-inflammatory, and antiapoptotic effects."( Can troxerutin pretreatment prevent testicular complications in prepubertal diabetic male rats?
Ahmadi, M; Bavil, FM; Ghadiri, A; Hamidian, GR; Keyhanmanesh, R; Oghbaei, H; Oskuye, ZZ, 2020
)
1.84
"Troxerutin has been reported to have cardioprotective functions."( Troxerutin attenuates oxygen‑glucose deprivation and reoxygenation‑induced oxidative stress and inflammation by enhancing the PI3K/AKT/HIF‑1α signaling pathway in H9C2 cardiomyocytes.
Hua, X; Li, C; Li, J; Sheng, XS; Yu, HQ; Yu, ZP, 2020
)
2.72

Treatment

Troxerutin-pretreatment may play an essential role in the management of the type-1 diabetes-induced testicular disorders by decreasing blood glucose and modulating apoptosis. TroxerutIn alleviated OGD/R‑induced oxidative stress.

ExcerptReferenceRelevance
"Troxerutin treatment attenuated oxidative stress in the hippocampus of diabetic rats, as evidenced by the decreased MDA level and the increased SOD activity."( Troxerutin attenuates cognitive decline in the hippocampus of male diabetic rats by inhibiting NADPH oxidase and activating the Nrf2/ARE signaling pathway.
Gao, M; Kang, Y; Li, H; Liu, L; Luan, X; Qu, C; Zhang, L; Zhang, S, 2020
)
2.72
"Troxerutin and insulin treatments were begun immediately on the day of diabetes confirmation."( Can troxerutin pretreatment prevent testicular complications in prepubertal diabetic male rats?
Ahmadi, M; Bavil, FM; Ghadiri, A; Hamidian, GR; Keyhanmanesh, R; Oghbaei, H; Oskuye, ZZ, 2020
)
1.84
"Troxerutin treatment improved these alterations compared to the diabetic group."( Can troxerutin pretreatment prevent testicular complications in prepubertal diabetic male rats?
Ahmadi, M; Bavil, FM; Ghadiri, A; Hamidian, GR; Keyhanmanesh, R; Oghbaei, H; Oskuye, ZZ, 2020
)
1.84
"Troxerutin-pretreatment may play an essential role in the management of the type-1 diabetes-induced testicular disorders by decreasing blood glucose and modulating apoptosis."( Can troxerutin pretreatment prevent testicular complications in prepubertal diabetic male rats?
Ahmadi, M; Bavil, FM; Ghadiri, A; Hamidian, GR; Keyhanmanesh, R; Oghbaei, H; Oskuye, ZZ, 2020
)
2.56
"Troxerutin pretreatment alleviated OGD/R‑induced oxidative stress, as demonstrated by the reduced generation of reactive oxygen species and malonaldehyde content, and the increased activities of superoxide dismutase and glutathione peroxidase, which were reduced by HIF‑1α‑siRNA."( Troxerutin attenuates oxygen‑glucose deprivation and reoxygenation‑induced oxidative stress and inflammation by enhancing the PI3K/AKT/HIF‑1α signaling pathway in H9C2 cardiomyocytes.
Hua, X; Li, C; Li, J; Sheng, XS; Yu, HQ; Yu, ZP, 2020
)
2.72
"Troxerutin treatment significantly suppressed STAT3/RNF6 signaling."( The bioflavonoid troxerutin prevents gestational hypertension in mice by inhibiting STAT3 signaling.
Duan, B; Li, Y; Sun, Q; Wang, Y; Yang, X, 2021
)
1.68
"Troxerutin treatment reduced the blood glucose and glycosylated hemoglobin levels in high-cholesterol-induced insulin-resistant mice and in type-2 diabetic patients."( Effect of troxerutin on insulin signaling molecules in the gastrocnemius muscle of high fat and sucrose-induced type-2 diabetic adult male rat.
Karundevi, B; Sampath, S, 2014
)
1.53
"When troxerutin pre-treated DU145 and PC3 cells were exposed to γ-radiation, cytotoxicity as estimated by MTT assay, was found to be further enhanced."( Troxerutin, a natural flavonoid binds to DNA minor groove and enhances cancer cell killing in response to radiation.
Ghaskadbi, SS; Maurya, DK; Panat, NA; Sandur, SK; Singh, BG, 2016
)
2.33
"Troxerutin was treated by daily oral administration at doses of 150 mg/kg/day for 20 weeks."( Troxerutin Attenuates Enhancement of Hepatic Gluconeogenesis by Inhibiting NOD Activation-Mediated Inflammation in High-Fat Diet-Treated Mice.
Fan, S; Lu, J; Shan, Q; Su, W; Sui, J; Sun, C; Wang, X; Wu, D; Zhang, C; Zhang, Z; Zheng, G; Zheng, Y, 2016
)
2.6
"Pretreatment with troxerutin as well as postconditioning can induce cardioprotection through prevention of the cell-cell interaction and release of inflammatory mediators, minimizing I/R pathological changes in myocardial cells."( Troxerutin Preconditioning and Ischemic Postconditioning Modulate Inflammatory Response after Myocardial Ischemia/Reperfusion Injury in Rat Model.
Abbaszadeh, A; Alihemmati, A; Badalzadeh, R; Baradaran, B; Yousefi, B, 2017
)
2.22
"Pretreatment with troxerutin resulted in a significantly higher 30-day survival rate for 70% of mice compared with 30% of irradiation group after exposure to a potentially lethal dose of 8 Gy; LD50/30 of drug treatment group was 9 Gy compared with 7.7 Gy for irradiation group. "( Radioprotective effects of troxerutin against gamma irradiation in mice liver.
Enjin, J; Junfeng, J; Junqing, J; Ping, X, 2012
)
1.01

Toxicity

ExcerptReferenceRelevance
" Adverse drug reactions were assessed regarding causality."( Safety aspects of a coumarin-troxerutin combination regarding liver function in a double-blind placebo-controlled study.
Becker, EW; Henneicke-von Zepelin, HH; Naser-Hijazi, B; Schmeck-Lindenau, HJ; Schnitker, J, 2003
)
0.61
"No serious adverse drug reactions occurred."( Safety aspects of a coumarin-troxerutin combination regarding liver function in a double-blind placebo-controlled study.
Becker, EW; Henneicke-von Zepelin, HH; Naser-Hijazi, B; Schmeck-Lindenau, HJ; Schnitker, J, 2003
)
0.61

Pharmacokinetics

ExcerptReferenceRelevance
" The maximal pharmacodynamic effects appeared simultaneous with the plasma drug peak."( Pharmacodynamics of troxerutine in patients with chronic venous insufficiency: correlations with plasma drug levels.
Auteri, A; Blardi, P; de Lillo, L; di Perri, T; Frigerio, C, 1990
)
0.6
" The primary objective was to evaluate the pharmacokinetic parameters, in particular the rate and extent of absorption (bioavailability) of two markers of Venoruton: mono-3'-HR and mono-4'-HR derivatives [glucuroconjugated forms (HG)], analysed in their deconjugated form as O-(beta-hydroxyethyl)-quercetin (HQ): mono-3'-HQ and mono-4'-HQ, and to investigate dose proportionality."( Pharmacokinetics of mono-3'- and mono-4'-0-(beta-hydroxyethyl)-rutoside derivatives, after single doses of Venoruton powder in healthy volunteers.
Ghika, A; Kienzler, JL; Sallin, D; Schifflers, MH, 2002
)
0.31
" Time to peak concentration of both Venoruton derivatives remained unaffected by the administered dose."( Pharmacokinetics of mono-3'- and mono-4'-0-(beta-hydroxyethyl)-rutoside derivatives, after single doses of Venoruton powder in healthy volunteers.
Ghika, A; Kienzler, JL; Sallin, D; Schifflers, MH, 2002
)
0.31
" The rate of appearance and the elimination half-life of both molecules were not modified with the administered dose."( Pharmacokinetics of mono-3'- and mono-4'-0-(beta-hydroxyethyl)-rutoside derivatives, after single doses of Venoruton powder in healthy volunteers.
Ghika, A; Kienzler, JL; Sallin, D; Schifflers, MH, 2002
)
0.31

Bioavailability

The W/O microemulsion can significantly promote the intestinal absorption of troxerutin in rats in vivo. The relative bioavailability of the microemulsions was about 205.

ExcerptReferenceRelevance
" The relative bioavailability of the drug from Venelbin was 97."( [HPLC determination of troxerutin in plasma and urine following oral administration in man].
Beubler, E; Dittrich, P; Kukovetz, W; Ostrowski, J; Schraven, E, 1985
)
0.58
"The bioavailability of both Venoruton derivatives (mono-3'-HQ and mono-4'-HQ) tended to be proportional to the dose."( Pharmacokinetics of mono-3'- and mono-4'-0-(beta-hydroxyethyl)-rutoside derivatives, after single doses of Venoruton powder in healthy volunteers.
Ghika, A; Kienzler, JL; Sallin, D; Schifflers, MH, 2002
)
0.31
" The W/O microemulsion can significantly promote the intestinal absorption of troxerutin in rats in vivo, and the relative bioavailability of the microemulsion was about 205."( Development and in vitro-in vivo evaluation of a water-in-oil microemulsion formulation for the oral delivery of troxerutin.
Chen, W; Jin, Y; Lin, Y; Xu, M; Yu, Q; Zhao, Q, 2016
)
0.87
"These results suggest that novel W/O microemulsion could be used as an effective formulation for improving the oral bioavailability of troxerutin."( Development and in vitro-in vivo evaluation of a water-in-oil microemulsion formulation for the oral delivery of troxerutin.
Chen, W; Jin, Y; Lin, Y; Xu, M; Yu, Q; Zhao, Q, 2016
)
0.85
"A facile and efficient whole-cell biocatalysis method was developed to synthesize troxerutin-acylated derivatives, markedly enhancing the bioavailability and antioxidant activities of troxerutin in cells."( Biocatalytic synthesis of acylated derivatives of troxerutin: their bioavailability and antioxidant properties in vitro.
Lai, F; Li, X; Xin, X; Zhang, M; Zhao, G, 2018
)
0.96
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51

Dosage Studied

Four simple, accurate, sensitive and precise spectrophotometric methods were developed and validated for simultaneous determination of Troxerutin (TXN) and Carbazochrome (CZM) in their bulk powders, laboratory prepared mixtures and pharmaceutical dosage forms.

ExcerptRelevanceReference
" These data were confirmed by excellent acceptability as well as subjective assessment by patients after 4 months' treatment at the dosage of 4 g/d."( [Clinical and rheological efficacy of troxerutin in obstetric gynecology].
Marhic, C, 1991
)
0.55
" These data indicate that the intraarterial infusion of Venoruton at this dosage does not inhibit the ability of simultaneously infused histamine or bradykinin to increase transvascular fluid and macromolecular efflux in the canine forelimb perfused at constant arterial inflow."( O-(beta-hydroxyethyl)-rutoside (Venoruton) fails to block histamine or bradykinin-induced edema formation in the canine forelimb perfused at constant arterial inflow.
Dabney, JM; Dobbins, DE; Soika, CY, 1984
)
0.27
" This proposed method was successfully applied to the detection of troxerutin in pharmaceutical dosage forms and satisfying results had been obtained."( The electrochemical oxidation of troxerutin and its sensitive determination in pharmaceutical dosage forms at PVP modified carbon paste electrode.
Hu, S; Wang, F; Yang, X, 2006
)
0.85
"05) were obtained in the group using the higher dosage and the associated treatment."( Clinical improvement in chronic venous insufficiency signs and symptoms with Venoruton® (HR): an 8-month, open-registry, cost-efficacy study.
Bavera, P; Belcaro, G; Cesarone, MR; Corsi, M; Dugall, M; Hosoi, M; Ippolito, E; Ledda, A; Luzzi, R; Pellegrini, L; Ricci, A; Stuard, S, 2010
)
0.36
"05) in the HR-treated groups with a significant decrease in edema score and ankle circumference in the higher dosage group."( Venoruton®: post thrombotic syndrome. Clinical improvement in venous insufficiency (signs and symptoms) with Venoruton®. A five-year, open-registry, efficacy study.
Bavera, P; Belcaro, G; Cesarone, MR; Corsi, M; Dugall, M; Errichi, BM; Errichi, S; Feragalli, B; Gizzi, G; Hosoi, M; Ippolito, E; Ledda, A; Luzzi, R; Pellegrini, L; Ricci, A, 2011
)
0.37
"Four simple, accurate, sensitive and precise spectrophotometric methods were developed and validated for simultaneous determination of Troxerutin (TXN) and Carbazochrome (CZM) in their bulk powders, laboratory prepared mixtures and pharmaceutical dosage forms."( Validated spectrophotometric methods for simultaneous determination of troxerutin and carbazochrome in dosage form.
Al-Ghobashy, MA; Ghoniem, NS; Hegazy, MA; Khattab, FI; Ramadan, NK, 2015
)
0.85
" Group I (control group), group II (rotenone treated group): the rats were injected subcutaneously with a single rotenone dosage of 3 mg/kg repeated every 48 hours for 60 days to trigger retinal neurodegeneration."( Troxerutin downregulates C/EBP-β gene expression via modulating the IFNγ-ERK1/2 signaling pathway to ameliorate rotenone-induced retinal neurodegeneration.
El-Esawy, RO; El-Sakaa, MH; Ibrahim, RR, 2020
)
2
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
estrogen nuclear receptor alphaHomo sapiens (human)Potency26.80620.000229.305416,493.5996AID743075
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (6)

Assay IDTitleYearJournalArticle
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1159550Human Phosphogluconate dehydrogenase (6PGD) Inhibitor Screening2015Nature cell biology, Nov, Volume: 17, Issue:11
6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling.
AID977602Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID977599Inhibition of sodium fluorescein uptake in OATP1B1-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (250)

TimeframeStudies, This Drug (%)All Drugs %
pre-199048 (19.20)18.7374
1990's36 (14.40)18.2507
2000's44 (17.60)29.6817
2010's92 (36.80)24.3611
2020's30 (12.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 62.13

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index62.13 (24.57)
Research Supply Index5.81 (2.92)
Research Growth Index4.77 (4.65)
Search Engine Demand Index103.94 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (62.13)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials58 (21.25%)5.53%
Reviews14 (5.13%)6.00%
Case Studies4 (1.47%)4.05%
Observational0 (0.00%)0.25%
Other197 (72.16%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (2)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Resolution Enhancement by a Supplemental Obstruction Lessening Venoactive Drug for Eight Weeks in Deep Vein Thrombosis: A Pilot Study to Evaluate if Hydroxyethylrutoside Reduces the Risk of Post-Thrombotic Syndrome in Patients With DVT. [NCT04670432]Phase 344 participants (Anticipated)Interventional2020-12-08Active, not recruiting
Evaluation of Efficacy and Safety of the Fixed-dose Combination of Coumarin and Troxerutin (Venalot®) Versus Placebo in the Symptomatic Treatment of Chronic Venous Insufficiency - VENACT [NCT01848210]Phase 4829 participants (Actual)Interventional2013-05-31Completed
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT01848210 (4) [back to overview]Change (Reduction) From Baseline in Local Complaint Severity
NCT01848210 (4) [back to overview]Mean Change (Reduction) From Baseline in Volume of Reference Leg at Week 16
NCT01848210 (4) [back to overview]Number of Participants With Adverse Events (AEs)
NCT01848210 (4) [back to overview]Overall Assessment by the Investigator

Change (Reduction) From Baseline in Local Complaint Severity

"Local Complaint Severity will be assessed using the Severity Score of Local Complaints that comprises 8 items: 1=tired legs, 2=heavy legs, 3= feeling of tension, 4=feeling of swelling, 5=aching legs, 6=tingling, 7=itching, 8=burning of soles of the feet.~Each item is classified with a Likert-type scale of 5 levels, where 0=absent, 1=low, 2=medium, 3=high, 4=very high.~A total score is calculated from the sum of the scores of all the 8 items and ranges from 0 (complaints absent) to 32 (very high severity)." (NCT01848210)
Timeframe: Baseline and Week 16

Interventionscore on a scale (Mean)
Coumarin + Troxerutin10.83
Placebo10.45

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Mean Change (Reduction) From Baseline in Volume of Reference Leg at Week 16

Change in the partial volume of legs will be measured using a water plethysmometer. The volume of water (at 34 ± 0.2 °C) displaced after limb immersion is collected in an empty plastic Beaker which has been previously weighed (scale tare). The equilibrium/stability will be estimated using the absolute difference between measures of volume obtained at the Week 16 visit and Baseline to determine the reduction in edema. (NCT01848210)
Timeframe: Baseline and Week 16

Interventionmilliliters (mL) (Mean)
Coumarin + Troxerutin1.13
Placebo5.78

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Number of Participants With Adverse Events (AEs)

Adverse events are any unwanted medical occurrences in an individual taking part in a clinical study who is receiving a pharmaceutical product. The adverse event does not have necessarily a causal relationship with the treatment. In this definition, any adverse or unwanted signals and symptoms, or findings that appear from the start or that deteriorate during the clinical study are also included, i.e. any intercurrent diseases (recently diagnosed concomitant diseases or symptoms), accidents and clinically relevant changes in clinical laboratory values. (NCT01848210)
Timeframe: Baseline to Week 16

Interventionparticipants (Number)
Coumarin + Troxerutin131
Placebo120

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Overall Assessment by the Investigator

The investigator recorded their impression of the overall clinical picture at the end of the treatment period (Week 16), taking into account the clinical picture compared with the Baseline visit. Data is reported for the percentage of participants in each of the following assessment categories: worsening, unchanged, discreet improvement or accentuated improvement. (NCT01848210)
Timeframe: Baseline and Week 16

,
Interventionpercentage of participants (Number)
WorseningUnchangedDiscreet improvementAccentuated improvement
Coumarin + Troxerutin0.611.225.362.9
Placebo0.814.324.460.4

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