Details
Stereochemistry | ACHIRAL |
Molecular Formula | C16H13N3O3 |
Molecular Weight | 295.2927 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC(=O)NC1=NC2=CC=C(C=C2N1)C(=O)C3=CC=CC=C3
InChI
InChIKey=OPXLLQIJSORQAM-UHFFFAOYSA-N
InChI=1S/C16H13N3O3/c1-22-16(21)19-15-17-12-8-7-11(9-13(12)18-15)14(20)10-5-3-2-4-6-10/h2-9H,1H3,(H2,17,18,19,21)
Molecular Formula | C16H13N3O3 |
Molecular Weight | 295.2927 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: https://www.drugs.com/pro/mebendazole.html
Sources: https://www.drugs.com/pro/mebendazole.html
Mebendazole, known as Emverm is a (synthetic) broad-spectrum anthelmintic that acts by interfering with carbohydrate metabolism and inhibiting polymerization of microtubules. The loss of the cytoplasmic microtubules leads to impaired uptake of glucose by the larval and adult stages of the susceptible parasites, and depletes their glycogen stores. Degenerative changes in the endoplasmic reticulum, the mitochondria of the germinal layer, and the subsequent release of lysosomes result in decreased production of adenosine triphosphate (ATP), which is the energy required for the survival of the helminth. Due to diminished energy production, the parasite is immobilized and eventually dies. Emverm tablets are used for the treatment of Enterobius vermicularis (pinworm), Trichuris trichiura (whipworm), Ascaris lumbricoides (common roundworm), Ancylostoma duodenale (common hookworm), Necator americanus (American hookworm) in single or mixed infections. All metabolites are devoid of anthelmintic activity. In man, approximately 2% of administered mebendazole is excreted in urine and the remainder in the feces as unchanged drug or a primary metabolite. Preliminary evidence suggests that cimetidine inhibits mebendazole metabolism and may result in an increase in plasma concentrations drug. Mebendazole sometimes causes diarrhea, abdominal pain, and elevated liver enzymes. In rare cases, it has been associated with a dangerously low white blood cell count, low platelet count, and hair loss, with a risk of agranulocytosis in rare cases
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL2364705 Sources: https://www.ncbi.nlm.nih.gov/pubmed/8139621 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Curative | EMVERM Approved UseEmverm™ (mebendazole) chewable tablet, USP is indicated for the treatment of Enterobius vermicularis (pinworm), Trichuris trichiura (whipworm), Ascaris lumbricoides (common roundworm), Ancylostoma duodenale (common hookworm), Necator americanus (American hookworm) in single or mixed infections. Launch Date7.8917763E11 |
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Curative | EMVERM Approved UseEmverm™ (mebendazole) chewable tablet, USP is indicated for the treatment of Enterobius vermicularis (pinworm), Trichuris trichiura (whipworm), Ascaris lumbricoides (common roundworm), Ancylostoma duodenale (common hookworm), Necator americanus (American hookworm) in single or mixed infections. Launch Date7.8917763E11 |
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Curative | EMVERM Approved UseEmverm™ (mebendazole) chewable tablet, USP is indicated for the treatment of Enterobius vermicularis (pinworm), Trichuris trichiura (whipworm), Ascaris lumbricoides (common roundworm), Ancylostoma duodenale (common hookworm), Necator americanus (American hookworm) in single or mixed infections. Launch Date7.8917763E11 |
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Curative | EMVERM Approved UseEmverm™ (mebendazole) chewable tablet, USP is indicated for the treatment of Enterobius vermicularis (pinworm), Trichuris trichiura (whipworm), Ascaris lumbricoides (common roundworm), Ancylostoma duodenale (common hookworm), Necator americanus (American hookworm) in single or mixed infections. Launch Date7.8917763E11 |
Cmax
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
14 ng/mL |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
MEBENDAZOLE plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
|
69.5 ng/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/7094986 |
10 mg/kg single, oral dose: 10 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
MEBENDAZOLE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FED |
AUC
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
175 ng × h/mL |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
MEBENDAZOLE plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
|
280.2 ng × h/mL EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/7094986 |
10 mg/kg single, oral dose: 10 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
MEBENDAZOLE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FED |
T1/2
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
3.6 h EXPERIMENT https://www.ncbi.nlm.nih.gov/pubmed/7094986 |
10 mg/kg single, oral dose: 10 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
MEBENDAZOLE plasma | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE / MALE food status: FED |
Funbound
Value | Dose | Co-administered | Analyte | Population |
---|---|---|---|---|
7.5% |
500 mg single, oral dose: 500 mg route of administration: Oral experiment type: SINGLE co-administered: |
MEBENDAZOLE plasma | Homo sapiens population: HEALTHY age: ADULT sex: UNKNOWN food status: FASTED |
Doses
Dose | Population | Adverse events |
---|---|---|
1600 mg 3 times / day multiple, oral MTD Dose: 1600 mg, 3 times / day Route: oral Route: multiple Dose: 1600 mg, 3 times / day Co-administed with:: CCNU, p.o(110 mg/m2; Day 1 for a 42 days cycle) Sources: Page: p.4681 |
unhealthy, 25-68 n = 4 Health Status: unhealthy Condition: Glioblastoma Age Group: 25-68 Sex: M+F Population Size: 4 Sources: Page: p.4681 |
DLT: Neutropenia, Thrombocytopenia... Dose limiting toxicities: Neutropenia (grade 4, 25%) Sources: Page: p.4681Thrombocytopenia (grade 3, 25%) |
500 mg single, oral Recommended Dose: 500 mg Route: oral Route: single Dose: 500 mg Co-administed with:: Metronidazole Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Gastrointestinal infections caused by Ascaris lumbricoides and Trichuris trichiura Sources: Page: p.1 |
Disc. AE: Stevens-Johnson syndrome, Toxic epidermal necrolysis... AEs leading to discontinuation/dose reduction: Stevens-Johnson syndrome (serious) Sources: Page: p.1Toxic epidermal necrolysis (serious) |
500 mg single, oral Recommended Dose: 500 mg Route: oral Route: single Dose: 500 mg Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Gastrointestinal infections caused by Ascaris lumbricoides and Trichuris trichiura Sources: Page: p.1 |
Disc. AE: Convulsions, Neutropenia... AEs leading to discontinuation/dose reduction: Convulsions Sources: Page: p.1Neutropenia Agranulocytosis |
AEs
AE | Significance | Dose | Population |
---|---|---|---|
Thrombocytopenia | grade 3, 25% DLT |
1600 mg 3 times / day multiple, oral MTD Dose: 1600 mg, 3 times / day Route: oral Route: multiple Dose: 1600 mg, 3 times / day Co-administed with:: CCNU, p.o(110 mg/m2; Day 1 for a 42 days cycle) Sources: Page: p.4681 |
unhealthy, 25-68 n = 4 Health Status: unhealthy Condition: Glioblastoma Age Group: 25-68 Sex: M+F Population Size: 4 Sources: Page: p.4681 |
Neutropenia | grade 4, 25% DLT |
1600 mg 3 times / day multiple, oral MTD Dose: 1600 mg, 3 times / day Route: oral Route: multiple Dose: 1600 mg, 3 times / day Co-administed with:: CCNU, p.o(110 mg/m2; Day 1 for a 42 days cycle) Sources: Page: p.4681 |
unhealthy, 25-68 n = 4 Health Status: unhealthy Condition: Glioblastoma Age Group: 25-68 Sex: M+F Population Size: 4 Sources: Page: p.4681 |
Stevens-Johnson syndrome | serious Disc. AE |
500 mg single, oral Recommended Dose: 500 mg Route: oral Route: single Dose: 500 mg Co-administed with:: Metronidazole Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Gastrointestinal infections caused by Ascaris lumbricoides and Trichuris trichiura Sources: Page: p.1 |
Toxic epidermal necrolysis | serious Disc. AE |
500 mg single, oral Recommended Dose: 500 mg Route: oral Route: single Dose: 500 mg Co-administed with:: Metronidazole Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Gastrointestinal infections caused by Ascaris lumbricoides and Trichuris trichiura Sources: Page: p.1 |
Agranulocytosis | Disc. AE | 500 mg single, oral Recommended Dose: 500 mg Route: oral Route: single Dose: 500 mg Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Gastrointestinal infections caused by Ascaris lumbricoides and Trichuris trichiura Sources: Page: p.1 |
Convulsions | Disc. AE | 500 mg single, oral Recommended Dose: 500 mg Route: oral Route: single Dose: 500 mg Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Gastrointestinal infections caused by Ascaris lumbricoides and Trichuris trichiura Sources: Page: p.1 |
Neutropenia | Disc. AE | 500 mg single, oral Recommended Dose: 500 mg Route: oral Route: single Dose: 500 mg Sources: Page: p.1 |
unhealthy Health Status: unhealthy Condition: Gastrointestinal infections caused by Ascaris lumbricoides and Trichuris trichiura Sources: Page: p.1 |
Overview
CYP3A4 | CYP2C9 | CYP2D6 | hERG |
---|---|---|---|
Drug as perpetrator
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: 12.0 |
likely | yes (co-administration study) Comment: ritonavir decreased mebendazole auc 43% and cmax 41% Page: 12.0 |
||
Page: 23.0 |
minor | |||
Page: 23.0 |
no | |||
Page: abstract |
no | |||
Page: abstract |
no | |||
Page: 23.0 |
no | |||
Page: 89.0 |
no | |||
Page: abstract |
yes |
Drug as victim
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: 1000.0 |
likely | |||
Page: 89.0 |
likely |
Tox targets
Target | Modality | Activity | Metabolite | Clinical evidence |
---|---|---|---|---|
Page: 11.0 |
PubMed
Title | Date | PubMed |
---|---|---|
[Mass chemotherapy for intestinal helminth infections in primary and secondary school students in Maoming city]. | 2001 |
|
[Efficacy of ablendazole emulsion in treatment of 212 patients with cystic echinococcosis]. | 2001 |
|
[Vomiting in an immigrant during early pregnancy]. | 2001 |
|
Optimising the benefits of anthelmintic treatment in children. | 2001 |
|
Eosinophilic meningitis caused by Angiostrongylus cantonensis: report of 17 cases. | 2001 Aug |
|
Ecchymoses: an unusual manifestation of toxocariasis in children. | 2001 Dec |
|
[Toxocariasis]. | 2001 Dec |
|
A female with cough, dyspnoea and chest pain. | 2001 Dec |
|
TLC determination of mebendazol and pentoxifylline as residues on pharmaceutical equipment surfaces. | 2001 Jul-Aug |
|
Treatment of Toxocara canis infections in mice with liposome-incorporated benzimidazole carbamates and immunomodulator glucan. | 2001 Jun |
|
Geo-helminth infections in a rural area of Sri Lanka. | 2001 Mar |
|
Echinococcal cysts of the liver: epidemiology, imaging classification, diagnosis and management. | 2001 May-Jun |
|
[Orthopedic aspects of osseous echinococcosis--radiologic diagnosis, current surgery and drug therapy aspects]. | 2001 May-Jun |
|
[Neurotrichinosis]. | 2001 Sep-Oct |
|
[Target chemotherapy of intestinal nematode infection in area with low endemicity]. | 2002 |
|
Musculoskeletal hydatid disease: a report of 13 cases. | 2002 Apr |
|
Maxillofacial hydatid cyst. | 2002 Apr |
|
Soil transmitted nematodes in children in Buea Health District of Cameroon. | 2002 Aug |
|
Two cases of imported gnathostomiasis in Spanish women. | 2002 Aug |
|
One-stage operation for hydatid disease of lung and liver: principles of treatment. | 2002 Dec |
|
Oxidative, heat and anthelminthic stress responses in four species of Trichinella: comparative study. | 2002 Dec 1 |
|
Pulmonary hydatidosis--a surgical experience. | 2002 Jan |
|
[Integrated treatment of iron deficiency, vitamin A deficiency and intestinal parasitic diseases: impact on Senegalese children's growth]. | 2002 Jan |
|
Chemotherapeutic approaches to nematodes: current knowledge and outlook. | 2002 Mar |
|
Clinical manifestations of strongyloidiasis in southern Taiwan. | 2002 Mar |
|
Is the exclusion of children under 24 months from anthelmintic treatment justifiable? | 2002 Mar-Apr |
|
Surgery and postoperative mebendazole in the treatment of hydatid disease. | 2002 May |
|
Infectious diseases of refugees and immigrants: hookworm. | 2002 May |
|
Surgery and postoperative mebendazole in the treatment of hydatid disease. | 2002 Nov |
|
The anthelmintic drug mebendazole induces mitotic arrest and apoptosis by depolymerizing tubulin in non-small cell lung cancer cells. | 2002 Nov |
|
[Adult ascaris in the intrahepatic bile ducts]. | 2002 Nov 9 |
|
Evaluation of the efficacy of pyrantel-oxantel for the treatment of soil-transmitted nematode infections. | 2002 Nov-Dec |
|
Case report: intraocular localization of Mansonella perstans in a patient from south Chad. | 2002 Nov-Dec |
|
Efficacy of alebendazole and mebendazole in the treatment of Ascaris and Trichuris infections. | 2002 Oct |
|
Soil-transmitted nematode infections and mebendazole treatment in Mafia Island schoolchildren. | 2002 Oct |
|
A randomized placebo-controlled trial of mebendazole for halitosis. | 2002 Oct |
|
[An outbreak of trichinosis in the Kaliningrad region]. | 2002 Oct-Dec |
|
Laparoscopic treatment of hepatic hydatid cysts with a liposuction device. | 2002 Oct-Dec |
|
New policies for using anthelmintics in high risk groups. | 2002 Sep |
|
Evaluation of the Integrated Management of Childhood Illness guidelines for treatment of intestinal helminth infections among sick children aged 2-4 years in western Kenya. | 2002 Sep-Oct |
|
Developing a discriminating dissolution test for three mebendazole polymorphs based on solubility differences. | 2003 Feb |
|
Benzimidazole treatment of cystic echinococcosis. | 2003 Feb |
|
Hydatid cyst of the liver-criteria for the selection of appropriate treatment. | 2003 Feb |
|
Pharmacokinetic evaluation of guar gum-based colon-targeted drug delivery systems of mebendazole in healthy volunteers. | 2003 Feb 14 |
|
Ascaris lumbricoides? | 2003 Jan |
|
Pregnancy outcome after gestational exposure to mebendazole: a prospective controlled cohort study. | 2003 Jan |
|
Use of anthelminthic drugs during pregnancy. | 2003 Jan |
|
In vitro studies on the effects of flubendazole against Toxocara canis and Ascaris suum. | 2003 Jan |
|
European echinococcosis registry: human alveolar echinococcosis, Europe, 1982-2000. | 2003 Mar |
|
Outbreak of Stevens-Johnson syndrome/toxic epidermal necrolysis associated with mebendazole and metronidazole use among Filipino laborers in Taiwan. | 2003 Mar |
Patents
Sample Use Guides
Pinworm (enterobiasis): 1 tablet, once; Whipworm (trichuriasis): 1 tablet morning and evening for 3 consecutive days; Common Roundworm (ascariasis): 1 tablet morning and evening for 3 consecutive days; Hookworm: 1 tablet morning and evening for 3 consecutive days
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/20848085
Curator's Comment: The release of interleukin (IL)-8 and tumor necrosis factor (TNF) α from human monocytic THP-1 cells was significantly increased by treatment with mebendazole (MBZ). MBZ also significantly increased the phosphorylation of extracellular signal-regulated kinase (ERK) 1/2 and c-Jun N-terminal kinase (JNK) 1/2 in THP-1 cells.
Unknown
Substance Class |
Chemical
Created
by
admin
on
Edited
Thu Jul 06 21:31:51 UTC 2023
by
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on
Thu Jul 06 21:31:51 UTC 2023
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Record UNII |
81G6I5V05I
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Record Status |
Validated (UNII)
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Record Version |
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CFR |
21 CFR 520.1320
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LIVERTOX |
NBK547885
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WHO-ATC |
P02CA01
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CFR |
21 CFR 520.1326A
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WHO-VATC |
QP52AC09
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WHO-ESSENTIAL MEDICINES LIST |
6.1.1
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NCI_THESAURUS |
C250
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CFR |
21 CFR 520.1326B
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WHO-ATC |
P02CA51
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EPA PESTICIDE CODE |
600073
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FDA ORPHAN DRUG |
397013
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FDA ORPHAN DRUG |
910922
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CFR |
21 CFR 520.1326
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NDF-RT |
N0000175481
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WHO-VATC |
QP52AC59
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C47595
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31431-39-7
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1641
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D008463
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1375502
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6704
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2942
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3232
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Mebendazole
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81G6I5V05I
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MEBENDAZOLE
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100000092064
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CHEMBL685
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DB00643
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81G6I5V05I
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250-635-4
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184849
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MEBENDAZOLE
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PRIMARY | Description: A white to slightly yellow powder. Solubility: Practically insoluble in water, dilute mineral acids, ethanol (~750 g/l) TS and ether R ; freely soluble in formic acid(~1080 g/l) TS. Category: Anthelmintic drug. Storage: Mebendazole should be kept in a well-closed container, protected from light. Additional information: Mebendazole exhibits polymorphism. Definition: Mebendazole is polymorph C, the crystal form of mebendazole RS. Mebendazole contains not less than 98.0% andnot more than 102.0% of mebendazole (C16H13N3O3), calculated with reference to the dried substance. | ||
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4030
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6672
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SUB08660MIG
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M7107
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DTXSID4040682
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (TITRATION)
USP
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BASIS OF STRENGTH->SUBSTANCE |
ASSAY (TITRATION)
EP
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METABOLITE INACTIVE -> PARENT | |||
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METABOLITE INACTIVE -> PARENT | |||
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METABOLITE INACTIVE -> PARENT |
MAJOR
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT | |||
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT | |||
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IMPURITY -> PARENT | |||
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IMPURITY -> PARENT | |||
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
For the calculation of contents, multiply the peak areas by 1.4
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT | |||
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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IMPURITY -> PARENT | |||
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IMPURITY -> PARENT |
Related Record | Type | Details | ||
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ACTIVE MOIETY |
Name | Property Type | Amount | Referenced Substance | Defining | Parameters | References |
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Volume of Distribution | PHARMACOKINETIC |
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Biological Half-life | PHARMACOKINETIC |
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