Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C2H5O3S2.Na |
| Molecular Weight | 164.179 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Na+].[O-]S(=O)(=O)CCS
InChI
InChIKey=XOGTZOOQQBDUSI-UHFFFAOYSA-M
InChI=1S/C2H6O3S2.Na/c3-7(4,5)2-1-6;/h6H,1-2H2,(H,3,4,5);/q;+1/p-1
| Molecular Formula | Na |
| Molecular Weight | 22.98976928 |
| Charge | 1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | C2H5O3S2 |
| Molecular Weight | 141.189 |
| Charge | -1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
DescriptionCurator's Comment: description was created based on several sources, including:
http://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8c79a07d-32cc-4fe7-9a74-152c169f1c4f
http://www.drugbank.ca/drugs/DB09110
https://en.wikipedia.org/wiki/Mesna
Curator's Comment: description was created based on several sources, including:
http://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=8c79a07d-32cc-4fe7-9a74-152c169f1c4f
http://www.drugbank.ca/drugs/DB09110
https://en.wikipedia.org/wiki/Mesna
Mesna is an organosulfur compound used as an adjuvant in cancer chemotherapy involving cyclophosphamide and ifosfamide. No clinical drug interaction studies have been conducted with mesna. Mesna concentrates in the bladder where acrolein accumulates after administration of chemotherapy and through a Michael addition, forms a conjugate with acrolein and other urotoxic metabolites. This conjugation reaction inactivates the urotoxic compounds to harmless metabolites. The most common adverse reactions (> 10%) when MESNEX is given with ifosfamide are nausea, vomiting, constipation, leukopenia, fatigue, fever, anorexia, thrombocytopenia, anemia, granulocytopenia, diarrhea, asthenia, abdominal pain, headache, alopecia, and somnolence.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL721: Aerolein |
|||
Target ID: CHEMBL733: 4-Hydroxyifosfamide |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Secondary | MESNEX Approved UseMesna Injection is indicated as a prophylactic agent in reducing the incidence of ifosfamide-induced hemorrhagic cystitis. Limitation of Use: Mesna Injection is not indicated to reduce the risk of hematuria due to other pathological conditions such as thrombocytopenia. Mesna Injection is a cytoprotective agent indicated as a prophylactic agent in reducing the incidence of ifosfamide-induced hemorrhagic cystitis. (1) Limitation of Use: Mesna Injection is not indicated to reduce the risk of hematuria due to other pathological conditions such as thrombocytopenia. (1) Launch Date1988 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
511 μM EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/8462128 |
1.2 g single, intravenous dose: 1.2 g route of administration: Intravenous experiment type: SINGLE co-administered: |
MESNA plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
33 μM EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/8462128 |
1.2 g single, oral dose: 1.2 g route of administration: Oral experiment type: SINGLE co-administered: |
MESNA plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
79 μM EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/9469350 |
0.24 g/m² single, intravenous dose: 0.24 g/m² route of administration: Intravenous experiment type: SINGLE co-administered: |
MESNA blood | Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
201 μM × h EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/8462128 |
1.2 g single, intravenous dose: 1.2 g route of administration: Intravenous experiment type: SINGLE co-administered: |
MESNA plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
110 μM × h EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/8462128 |
1.2 g single, oral dose: 1.2 g route of administration: Oral experiment type: SINGLE co-administered: |
MESNA plasma | Homo sapiens population: HEALTHY age: ADULT sex: FEMALE / MALE food status: FASTED |
|
49 μM × h EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/9469350 |
0.24 g/m² single, intravenous dose: 0.24 g/m² route of administration: Intravenous experiment type: SINGLE co-administered: |
MESNA blood | Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
92 min EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/9469350 |
0.24 g/m² single, intravenous dose: 0.24 g/m² route of administration: Intravenous experiment type: SINGLE co-administered: |
MESNA blood | Homo sapiens population: UNHEALTHY age: ADULT sex: MALE food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
Other AEs: Headache, Hypoaesthesia... Other AEs: Headache (43.8%) Sources: Hypoaesthesia (0%) Malaise (0%) Myalgia (0%) Nausea (0%) Pharyngitis (0%) Somnolence (6.3%) Upper respiratory infection (0%) Vomiting (0%) Dizziness (6.3%) Abdominal pain (6.3%) Coughing (0%) Diarrhea (6.3%) Anorexia (0%) Flushing (12.5%) Injection site reaction (12.5%) Back pain (6.3%) Dyspepsia (12.5%) Paraesthesia (6.3%) Renal pain (6.3%) Rigors (12.5%) Fatigue (0%) Conjunctivitis (6.3%) Arthralgia (12.5%) Application site reaction (31.3%) Photophobia (18.8%) Dehydration (6.3%) Dysuria (6.3%) Sweating increased (6.3%) |
2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
Other AEs: Headache, Hypoaesthesia... Other AEs: Headache (33.3%) Sources: Hypoaesthesia (0%) Malaise (8.3%) Myalgia (0%) Nausea (16.7%) Pharyngitis (0%) Somnolence (8.3%) Upper respiratory infection (0%) Vomiting (16.7%) Dizziness (8.3%) Abdominal pain (8.3%) Coughing (0%) Diarrhea (0%) Anorexia (8.3%) Flushing (0%) Injection site reaction (0%) Back pain (0%) Dyspepsia (0%) Paraesthesia (8.3%) Renal pain (0%) Rigors (0%) Fatigue (8.3%) Conjunctivitis (0%) Arthralgia (0%) Application site reaction (0%) Photophobia (0%) Dehydration (0%) Dysuria (0%) Sweating increased (0%) |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Anorexia | 0% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Coughing | 0% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Fatigue | 0% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Hypoaesthesia | 0% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Malaise | 0% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Myalgia | 0% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Nausea | 0% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Pharyngitis | 0% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Upper respiratory infection | 0% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Vomiting | 0% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Arthralgia | 12.5% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Dyspepsia | 12.5% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Flushing | 12.5% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Injection site reaction | 12.5% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Rigors | 12.5% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Photophobia | 18.8% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Application site reaction | 31.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Headache | 43.8% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Abdominal pain | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Back pain | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Conjunctivitis | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Dehydration | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Diarrhea | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Dizziness | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Dysuria | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Paraesthesia | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Renal pain | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Somnolence | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Sweating increased | 6.3% | 1200 mg single, intravenous Highest studied dose Dose: 1200 mg Route: intravenous Route: single Dose: 1200 mg Sources: |
healthy Health Status: healthy Sources: |
| Application site reaction | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Arthralgia | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Back pain | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Conjunctivitis | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Coughing | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Dehydration | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Diarrhea | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Dyspepsia | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Dysuria | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Flushing | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Hypoaesthesia | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Injection site reaction | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Myalgia | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Pharyngitis | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Photophobia | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Renal pain | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Rigors | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Sweating increased | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Upper respiratory infection | 0% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Nausea | 16.7% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Vomiting | 16.7% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Headache | 33.3% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Abdominal pain | 8.3% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Anorexia | 8.3% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Dizziness | 8.3% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Fatigue | 8.3% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Malaise | 8.3% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Paraesthesia | 8.3% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
| Somnolence | 8.3% | 2400 mg single, oral Highest studied dose Dose: 2400 mg Route: oral Route: single Dose: 2400 mg Sources: |
healthy Health Status: healthy Sources: |
PubMed
| Title | Date | PubMed |
|---|---|---|
| The cytogenetic action of ifosfamide, mesna, and their combination on peripheral rabbit lymphocytes: an in vivo/in vitro cytogenetic study. | 2014-10 |
|
| Comparision of uroprotective activity of reduced glutathione with mesna in ifosfamide induced hemorrhagic cystitis in rats. | 2013-07-01 |
|
| Surface functionalities of gold nanoparticles impact embryonic gene expression responses. | 2013-03 |
|
| Acrolein and chloroacetaldehyde: an examination of the cell and cell-free biomarkers of toxicity. | 2013-02-25 |
|
| Combined intravenous and oral mesna in outpatients treated with ifosfamide. | 1997 |
|
| Influence of mesna on urotoxic effects of selected bromosubstituted analogs of ifosfamide. | 1997 |
|
| Ifosfamide encephalopathy and methylene-blue: a case report. | 1996-08 |
|
| Continuous subcutaneous administration of mesna to prevent ifosfamide-induced hemorrhagic cystitis. | 1996-06 |
|
| [The prevention of hemorrhagic cystitis during the performance of bone marrow and peripheral blood stem cell transplantation in the hematologic cancer clinic]. | 1996 |
|
| [Ifosfamide-induced hemorrhagic cystitis and its prevention by mesna]. | 1995-06 |
|
| [Epileptic seizures and treatment with ifosfamide-mesna]. | 1994 |
|
| Encephalopathy with hyponatremia and inappropriate arginine vasopressin secretion following an intravenous ifosfamide infusion. | 1990 |
|
| Ifosfamide and mesna in the treatment of malignant disease mesna as urothelial protector. | 1989-07 |
|
| Chloroacetaldehyde and its contribution to urotoxicity during treatment with cyclophosphamide or ifosfamide. An experimental study/short communication. | 1989-06 |
|
| Treatment of gynecological adenocarcinomas with a combination of ifosfamide, adriamycin and cisplatin. | 1988-05 |
|
| [Encephalopathy caused by an ifosfamide-mesna combination]. | 1988-04-02 |
|
| Efficacy of mesna in preventing further cyclophosphamide-induced hemorrhagic cystitis. | 1988 |
|
| Ifosfamide/mesna related encephalopathy: a case report with a possible role of phenobarbital in enhancing neurotoxicity. | 1988 |
|
| Irreversible encephalopathy with ifosfamide/mesna. | 1987-08 |
|
| Ifosfamide with mesna uroprotection and etoposide: an effective regimen in the treatment of recurrent sarcomas and other tumors of children and young adults. | 1987-08 |
|
| The efficacy of mesna (2-mercaptoethane sodium sulfonate) as a uroprotectant in patients with hemorrhagic cystitis receiving further oxazaphosphorine chemotherapy. | 1987-05 |
|
| Ifosfamide/mesna encephalopathy. | 1987-04-25 |
|
| Ifosfamide neurotoxicity in children. | 1987-03 |
|
| Encephalopathy with rapid infusion ifosfamide/mesna. | 1987-02-14 |
|
| Ifosfamide-induced subclinical tubular nephrotoxicity despite mesna. | 1987-02 |
|
| Blurring of vision due to ifosfamide. | 1987 |
|
| Electron microscopic investigations of the cyclophosphamide-induced lesions of the urinary bladder of the rat and their prevention by mesna. | 1987 |
|
| Avoiding ifosfamide/mesna encephalopathy. | 1986-08-16 |
|
| Central nervous system toxicity following the treatment of pediatric patients with ifosfamide/mesna. | 1986-08 |
|
| Prediction of ifosfamide/mesna associated encephalopathy. | 1986-07 |
|
| The protective effect of 2-mercapto-ethane sulfonate (MESNA) on hemorrhagic cystitis induced by high-dose ifosfamide treatment tested by a randomized crossover trial. | 1986-06 |
|
| Phase II study of ifosfamide in cervical cancer. | 1986-06 |
|
| Cause and prevention of mafosfamide-induced venous pain. | 1986 |
|
| Ifosfamide plus mesna with and without adriamycin in soft tissue sarcoma. | 1986 |
|
| CNS-side effects induced by Ifosfamide-Mesna in children with osteosarcomas. | 1986 |
|
| Ifosfamide, mesna, and encephalopathy. | 1985-06-15 |
|
| Phase II trial of ifosfamide with mesna in previously treated metastatic sarcoma. | 1985-05 |
|
| Ifosfamide/mesa and encephalopathy. | 1985-03-30 |
|
| Encephalopathy associated with ifosphamide/mesna therapy. | 1985-02-16 |
|
| Comparison of mesna with forced diuresis to prevent cyclophosphamide induced haemorrhagic cystitis in marrow transplantation: a prospective randomised study. | 1984-12 |
|
| [Prevention of tumor formation in the bladder by sodium-2-mercaptoethane sulfonate (mesna). Experimental studies and clinical consequences]. | 1984-09 |
|
| Prevention of cyclophosphamide cystitis with 2-mercaptoethane sodium sulfonate: a histologic study. | 1984-09 |
|
| The use of sodium 2-mercaptoethane sulfonate to prevent cyclophosphamide cystitis. | 1984-05 |
|
| Prevention of cyclophosphamide-induced carcinogenesis in the urinary bladder of rats by administration of mesna. | 1983-09 |
|
| Experience with mesna in patients receiving allogeneic bone marrow transplants for poor prognostic leukaemia. | 1983-09 |
|
| Prevention of urinary bladder tumors in cyclophosphamide-treated rats by additional medication with the uroprotectors sodium 2-mercaptoethane sulfonate (mesna) and disodium 2,2'-dithio-bis-ethane sulfonate (dimesna). | 1983-02-15 |
|
| Treatment of ifosfamide-induced urothelial toxicity by oral administration of sodium 2-mercaptoethane sulphonate (MESNA) to patients with inoperable lung cancer. | 1983-02 |
|
| Mesnum as a protector against kidney and bladder toxicity with high-dose ifosfamide treatment. | 1982 |
|
| Detoxification of urotoxic oxazaphosphorines by sulfhydryl compounds. | 1981 |
|
| Prevention of isophosphamide-induced urothelial toxicity with 2-mercaptoethane sulphonate sodium (mesnum) in patients with advanced carcinoma. | 1980-09-27 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Wed Apr 02 09:59:48 GMT 2025
by
admin
on
Wed Apr 02 09:59:48 GMT 2025
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| Record UNII |
NR7O1405Q9
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| Record Status |
Validated (UNII)
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| Record Version |
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Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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FDA ORPHAN DRUG |
24887
Created by
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NDF-RT |
N0000180854
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NCI_THESAURUS |
C2082
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LIVERTOX |
606
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WHO-VATC |
QR05CB05
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WHO-VATC |
QV03AF01
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WHO-ATC |
V03AF01
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FDA ORPHAN DRUG |
8685
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WHO-ATC |
R05CB05
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WHO-ESSENTIAL MEDICINES LIST |
8.2
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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DTXSID1020809
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PRIMARY | |||
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m7249
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PRIMARY | Merck Index | ||
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1392807
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PRIMARY | |||
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C192
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NR7O1405Q9
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| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
PARENT -> SALT/SOLVATE |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
||
|
IMPURITY -> PARENT |
Correction factors: for the calculation of contents, multiply the peak areas by 0.01
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
||
|
IMPURITY -> PARENT |
Correction factors: for the calculation of contents, multiply the peak areas by 0.01
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
Correction factors: for the calculation of contents, multiply the peak areas by 0.01
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
||
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|
| Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
|---|---|---|---|---|---|---|
| Biological Half-life | PHARMACOKINETIC |
|
Elimination PHARMACOKINETIC |
|
||