Page last updated: 2024-11-11

glucuronyl glucosamine glycan sulfate

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Cross-References

ID SourceID
PubMed CID6453528
SCHEMBL ID665209
MeSH IDM0051290

Synonyms (32)

Synonym
n(6),o(2)-dimethyladenosine
(2r,3r,4r,5r)-2-(hydroxymethyl)-4-methoxy-5-[6-(methylamino)purin-9-yl]oxolan-3-ol
glucuronyl glucosamine glycan sulfate
unii-lev25j2gtv
lev25j2gtv ,
57817-83-1
75hgv0062c ,
sulodexidum [inn-latin]
krx-101
vessel 2f
provenal
vessel
gluparin
treparin
vessel due f
sulodexido
sulodexidum
sulodexide [inn]
sulodexido [inn-spanish]
glucorono-2-amino-2-deoxyglucoglucan sulfate
glucuronylglucosamineglicane sulfate
unii-75hgv0062c
SCHEMBL665209
DTXSID50206530
n6,2'-o-dimethyladenosine
n6-methyl-2'-o-methyladenosine
2'-o-methyl-6-methyladenosine
n6,2 inverted exclamation marka-o-dimethyladenosine
HY-101082
(2r,3r,4r,5r)-2-(hydroxymethyl)-4-methoxy-5-[6-(methylamino)-9h-purin-9-yl]oxolan-3-ol
n6,o2'-dimethyladenosine
CS-0020794

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Compliance with treatment and occurrence of adverse events were constantly monitored; systemic tolerability was evaluated through the use of routine haematological and haematochemical tests."( Controlled clinical trial on the efficacy and safety of oral sulodexide in patients with peripheral occlusive arterial disease.
Shustov, SB, 1997
)
0.3
" No differences between the groups were detected concerning demographic or basal characteristics in clinical evolution or adverse reactions."( A study on the safety, efficacy, and efficiency of sulodexide compared with acenocoumarol in secondary prophylaxis in patients with deep venous thrombosis.
Cirujeda, JL; Granado, PC,
)
0.13

Pharmacokinetics

ExcerptReferenceRelevance
" The compound showed a pharmacokinetic pattern similar to that of heparin and the plasmatic levels were linearly correlated with anti-factor Xa activity and logarithmically with lipoprotein lipase activation."( Pharmacokinetics and distribution of a fluoresceinated glycosaminoglycan, sulodexide, in rats. Part I: Pharmacokinetics in rats.
Barbanti, M; Cristofori, M; Mastacchi, R; Sarret, M, 1985
)
0.27

Bioavailability

ExcerptReferenceRelevance
" The low molecular weight (Mr) of the constituents of Sulodexide would predict that the product has the high bioavailability associated with low-Mr heparin and low-Mr dermatan sulfate."( Pharmacological actions of sulodexide.
Ofosu, FA, 1998
)
0.3
" Sulodexide differs from heparin because it is orally bioavailable and has a longer half-life and a smaller effect on systemic clotting and bleeding."( Sulodexide in the treatment of chronic venous disease.
Andreozzi, GM, 2012
)
0.38
" Sulodexide differs from heparin in its oral bioavailability and longer half-life."( Pharmacological profile of sulodexide.
Fareed, J; Hoppensteadt, DA, 2014
)
0.4

Dosage Studied

ExcerptRelevanceReference
"Fluorescein-labelled sulodexide tissue distribution was studied in the rat after intravenous administration at the dosage of 15 mg/kg."( Pharmacokinetics and distribution of a fluoresceinated glycosaminoglycan, sulodexide, in rats. Part II: Organ distribution in rats.
Franchi, M; Guizzardi, S; Mastacchi, R; Morocutti, M; Ruggeri, A, 1985
)
0.27
" The pro-fibrinolytic and antithrombotic activity of sulodexide was confirmed to be significant with both dosage schemes and potentiated by repeated administrations."( Pharmacodynamic effects of single and repeated doses of oral sulodexide in healthy volunteers. A placebo-controlled study with an enteric-coated formulation.
Barbanti, M; Calanni Rindina, F; Mauro, M; Milani, MR; Palazzini, E; Palmieri, GC, 1993
)
0.29
" Albumin excretion was measured before dosing, at weekly intervals during dosing and also during the subsequent follow-up period of six weeks."( A pilot study of the effect of the glycosaminoglycan sulodexide on microalbuminuria in type I diabetic patients.
Grimaldi, M; Jopdska, J; Kinalska, I; Poplawska, A; Szelachowska, M; Szelanowska, M; Topolska, J, 1997
)
0.3
"In this study we have evaluated the effect of a long-term course of oral sulodexide at a moderate dosage in the treatment of patients affected by diabetic nephropathy."( One year course of oral sulodexide in the management of diabetic nephropathy.
Achour, A; Bouraoui, S; Dibej, K; El May, M; Kacem, M; Skhiri, H,
)
0.13
"This study was carried out to study the safety and efficacy of a fixed dosage of sulodexide compared to adjusted dosages (INR) of acenocoumarol as secondary prophylaxis in patients with deep vein thrombosis (DVT) in lower limbs."( A study on the safety, efficacy, and efficiency of sulodexide compared with acenocoumarol in secondary prophylaxis in patients with deep venous thrombosis.
Cirujeda, JL; Granado, PC,
)
0.13
"This aspect of the retinal arterial or/and venous vessels requires laboratory blood dosing for antiphospholipid antibodies."( [Methods of prevention of ischemic cerebral damages in patients with antiphospholipid antibodies].
Roşca, T, 2008
)
0.35
" Similarly, SUL was able to reverse the hyper-expression of EMT markers induced by high EVE dosage (100 nM) in cells cultured under both normoxic and hypoxic conditions."( Sulodexide alone or in combination with low doses of everolimus inhibits the hypoxia-mediated epithelial to mesenchymal transition in human renal proximal tubular cells.
Bellin, G; Dalla Gassa, A; Gambaro, G; Granata, S; Lupo, A; Masola, V; Onisto, M; Zaza, G, 2015
)
0.42
"Our data reveal, for the first time, that sulodexide, alone or combined to low doses of everolimus, may hinder EMT in renal cells following hypoxia or minimize fibrotic complications due to high dosage of mammalian target of rapamycin inhibitors."( Sulodexide alone or in combination with low doses of everolimus inhibits the hypoxia-mediated epithelial to mesenchymal transition in human renal proximal tubular cells.
Bellin, G; Dalla Gassa, A; Gambaro, G; Granata, S; Lupo, A; Masola, V; Onisto, M; Zaza, G, 2015
)
0.42
" In this article by the Global COVID-19 Thrombosis Collaborative Group, we describe novel dosing approaches for commonly used antithrombotic agents (especially heparin-based regimens) and the potential use of less widely used antithrombotic drugs in the absence of confirmed thrombosis."( Pharmacological Agents Targeting Thromboinflammation in COVID-19: Review and Implications for Future Research.
Ageno, W; Barnes, GD; Batra, J; Beckman, JA; Bertoletti, L; Bikdeli, B; Burton, JR; Carrier, M; Chatterjee, S; Chuich, T; Clerkin, KJ; Cushman, M; Der Nigoghossian, C; Dimakakos, EP; Dreyfus, I; Driggin, E; Eikelboom, JW; Falanga, A; Fareed, J; Favaloro, EJ; Francese, DP; Gibson, CM; Giri, J; Goldhaber, SZ; Guo, Y; Gupta, A; Hu, Y; Hunt, BJ; Jimenez, D; Kirtane, A; Konstantinides, SV; Krumholz, HM; Leon, MB; Lip, GYH; Lippi, G; Madhavan, MV; Madjid, M; McLintock, C; Monreal, M; Nouri, SN; Parikh, SA; Piazza, G; Quéré, I; Rosenkranz, S; Schulman, S; Sehgal, K; Sethi, S; Spyropoulos, AC; Stone, GW; Tafur, AJ; Tang, LV; Uriel, N; Weinberg, I; Weitz, JI, 2020
)
0.56
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (250)

TimeframeStudies, This Drug (%)All Drugs %
pre-199029 (11.60)18.7374
1990's43 (17.20)18.2507
2000's39 (15.60)29.6817
2010's110 (44.00)24.3611
2020's29 (11.60)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 9.05

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index9.05 (24.57)
Research Supply Index5.90 (2.92)
Research Growth Index4.96 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (9.05)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials81 (28.52%)5.53%
Reviews41 (14.44%)6.00%
Case Studies9 (3.17%)4.05%
Observational5 (1.76%)0.25%
Other148 (52.11%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (16)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Effect of Intravenous and Oral Therapy With Sulodexide on Albuminuria in Type 2 Diabetic Patients [NCT01316068]Phase 480 participants (Anticipated)Interventional2011-03-31Enrolling by invitation
A Multicentre, Double-Blind, Randomised, Placebo Controlled Study of the Activity of Sulodexide in Diabetic Patients With Mild to Moderate Non-Proliferative Retinopathy [NCT01295775]Phase 2127 participants (Actual)Interventional2009-02-28Completed
The Collaborative Study Group Trial: The Effect of Sulodexide in Patients With Type 2 Diabetes and Microalbuminuria [NCT00130208]Phase 31,056 participants (Actual)Interventional2005-08-31Completed
Rotation for Optimal Targeting of Albuminuria and Treatment Evaluation: A Rotation Study of Different Albuminuria Lowering Drug Classes to Study Individual Drug Response in Diabetes [NCT03504566]Phase 40 participants (Actual)Interventional2017-11-15Withdrawn(stopped due to Registered and published incorrectly)
An Open Label Tolerability and Safety Study of KRX-101 (Sulodexide Gelcaps) for the Treatment of Type 2 Diabetic Nephropathic Patients With Persistent Microalbuminuria in Australia, New Zealand, and Hong Kong [NCT00462202]Phase 3200 participants (Actual)Interventional2007-04-30Terminated(stopped due to Interim analysis of efficacy trial showed no drug efficacy.)
The Study of Reducing Adverse Effects After Radiofrequency Ablation Combined With Sclerotherapy [NCT05654233]120 participants (Anticipated)Interventional2023-02-01Not yet recruiting
Randomized Double Blind Controlled Trial on Sulodexide Efficacy in Chronic Idiopathic Subjective Tinnitus [NCT02737670]Phase 2126 participants (Actual)Interventional2014-08-31Completed
Endothelial Protection in Post COVID-19 Patients. The Effect of Sulodexide on Serum Levels of Biomarkers for Endothelial Dysfunction. A Prospective, Randomized, Placebo-controlled, Investigator-initiated Trial [NCT05371925]Phase 3200 participants (Anticipated)Interventional2022-07-26Recruiting
Sulodexide (VESSEL®) for the Prevention of Recurrent Venous Thromboembolism in Elderly Patients After a First Episode of Venous Thrombembolism [NCT04257487]Phase 31,455 participants (Anticipated)Interventional2020-12-21Recruiting
Sulodexide Treatment in Patients With Dense Deposit Disease [NCT00583427]Phase 10 participants (Actual)Interventional2007-12-31Withdrawn(stopped due to This study put on inactive status due to no identifiable subjects to enter the protocol.)
Endothelial Protection in Convalescent COVID-19 Patients. The Effect of Sulodexide on Serum Levels of Biomarkers for Endothelial Dysfunction. A Pilot Prospective, Randomized, Open-label, Investigator-initiated Trial. [NCT05252923]Phase 430 participants (Anticipated)Interventional2022-04-01Recruiting
The Efficacy and Safety of Sulodexide in Filipino Diabetic Patients With Chronic Kidney Disease: A Randomized Controlled Trial [NCT01000545]Phase 31,508 participants (Anticipated)Interventional2009-11-30Not yet recruiting
The Collaborative Study Group Trial: The Effect of Sulodexide in Overt Type 2 Diabetic Nephropathy [NCT00130312]Phase 4968 participants (Actual)Interventional2005-08-31Terminated(stopped due to No difference in protein excretion at 6&12 months. No safety issues.)
Sulodexide in the Treatment of Early Stages of COVID-19 [NCT04483830]Phase 2/Phase 3243 participants (Actual)Interventional2020-06-05Completed
A Multicentric Open-label Randomized Controlled Study for Evaluating the Improvement of Endothelial Function in Stage II Peripheral Arterial Obstructive Disease Patients Treated With Sulodexide + Conventional Treatment {CT] Vs CT Alone [NCT03370705]Phase 3156 participants (Anticipated)Interventional2019-01-31Active, not recruiting
Prospective Evaluation of the Quality of Life of Patients With Post-thrombotic Syndrome Who Receive Compression Therapy and Sulodexide - SQUARES Study [NCT02512601]Phase 413 participants (Actual)Interventional2015-09-30Terminated(stopped due to Poor inclusion)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT00130208 (3) [back to overview]Change in Serum Albumin From Baseline to End of 26 Weeks
NCT00130208 (3) [back to overview]Number of Subjects With Conversion From Microalbuminuria to Normoalbuminuria
NCT00130208 (3) [back to overview]Number of Subjects With Greater Than 50% Reduction in Microalbuminuria

Change in Serum Albumin From Baseline to End of 26 Weeks

(NCT00130208)
Timeframe: 26 Weeks

Interventionpercent change (Least Squares Mean)
Sulodexide-0.02
Placebo-0.02

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Number of Subjects With Conversion From Microalbuminuria to Normoalbuminuria

"The primary efficacy variable was the fraction of those patients in the ITT population with valid baseline and Week 26 ACRs in whom therapeutic success was achieved at Week 26 measured as a conversion of microalbuminuria to normoalbuminuria and at least a 25% reduction in ACR relative to baseline" (NCT00130208)
Timeframe: 26 Weeks

InterventionParticipants (Count of Participants)
Sulodexide39
Placebo30

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Number of Subjects With Greater Than 50% Reduction in Microalbuminuria

During the treatment period, KRX-101 is being compared to placebo to assess whether a 50% reduction in microalbuminuria has been achieved. (NCT00130208)
Timeframe: 26 Weeks

InterventionParticipants (Count of Participants)
Sulodexide76
Placebo87

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