Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H7N3S |
| Molecular Weight | 201.248 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
N1C(=NC2=C1C=CC=C2)C3=CSC=N3
InChI
InChIKey=WJCNZQLZVWNLKY-UHFFFAOYSA-N
InChI=1S/C10H7N3S/c1-2-4-8-7(3-1)12-10(13-8)9-5-14-6-11-9/h1-6H,(H,12,13)
| Molecular Formula | C10H7N3S |
| Molecular Weight | 201.248 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Thiabendazole (TBZ, trade names Mintezol, Tresaderm, and Arbotect) was first introduced in 1962. This drug is a fungicide and parasiticide and is indicated for the treatment of: strongyloidiasis (threadworm), cutaneous larva migrans (creeping eruption), visceral larva migrans, trichinosis: relief of symptoms and fever and a reduction of eosinophilia have followed the use of this drug during the invasion stage of the disease. But usage of this drug was discontinued. The precise mode of action of thiabendazole on the parasite is unknown, but it may inhibit the helminthspecific enzyme fumarate reductase. It was shown, also that thiabendazole reversibly disassembles newly established blood vessels, marking it as vascular disrupting agent (VDA) and thus as a potential complementary therapeutic for use in combination with current anti-angiogenic therapies. Was shown, that vascular disruption by TBZ results from reduced tubulin levels and hyper-active Rho signaling. In addition, was confirmed, that thiabendazole slowed tumor growth and decreased vascular density in preclinical fibrosarcoma xenografts and thus, it could lead directly to the identification of a potential new therapeutic application for an inexpensive drug that is already approved for clinical use in humans.
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: CHEMBL2095182 Sources: https://www.ncbi.nlm.nih.gov/pubmed/22927795 |
|||
Target ID: O06913 Gene ID: 900116.0 Gene Symbol: frdA Target Organism: Helicobacter pylori (strain ATCC 700392 / 26695) (Campylobacter|||pylori) Sources: https://www.ncbi.nlm.nih.gov/pubmed/11031122 |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Curative | MINTEZOL Approved UseMINTEZOL is indicated for the treatment of: Strongyloidiasis (threadworm) Cutaneous larva migrans (creeping eruption) Visceral larva migrans
Trichinosis: Relief of symptoms and fever and a reduction of eosinophilia have followed the use of MINTEZOL during the invasion stage of the disease.Thiabendazole is usually inappropriate as first line therapy for enterobiasis (pinworm). However, when enterobiasis occurs with any of the conditions listed above, additional therapy is not required for most patients. MINTEZOL should be used only in the following infestations when more specific therapy is not available or cannot be used or when further therapy with a second agent is desirable: Uncinariasis (hookworm: Necator americanus and Ancylostoma duodenale); Trichuriasis (whipworm); Ascariasis (large roundworm). Launch Date1967 |
|||
| Curative | MINTEZOL Approved UseMINTEZOL is indicated for the treatment of: Strongyloidiasis (threadworm) Cutaneous larva migrans (creeping eruption) Visceral larva migrans
Trichinosis: Relief of symptoms and fever and a reduction of eosinophilia have followed the use of MINTEZOL during the invasion stage of the disease.Thiabendazole is usually inappropriate as first line therapy for enterobiasis (pinworm). However, when enterobiasis occurs with any of the conditions listed above, additional therapy is not required for most patients. MINTEZOL should be used only in the following infestations when more specific therapy is not available or cannot be used or when further therapy with a second agent is desirable: Uncinariasis (hookworm: Necator americanus and Ancylostoma duodenale); Trichuriasis (whipworm); Ascariasis (large roundworm). Launch Date1967 |
|||
| Curative | MINTEZOL Approved UseMINTEZOL is indicated for the treatment of: Strongyloidiasis (threadworm) Cutaneous larva migrans (creeping eruption) Visceral larva migrans
Trichinosis: Relief of symptoms and fever and a reduction of eosinophilia have followed the use of MINTEZOL during the invasion stage of the disease.Thiabendazole is usually inappropriate as first line therapy for enterobiasis (pinworm). However, when enterobiasis occurs with any of the conditions listed above, additional therapy is not required for most patients. MINTEZOL should be used only in the following infestations when more specific therapy is not available or cannot be used or when further therapy with a second agent is desirable: Uncinariasis (hookworm: Necator americanus and Ancylostoma duodenale); Trichuriasis (whipworm); Ascariasis (large roundworm). Launch Date1967 |
|||
| Curative | MINTEZOL Approved UseMINTEZOL is indicated for the treatment of: Strongyloidiasis (threadworm) Cutaneous larva migrans (creeping eruption) Visceral larva migrans
Trichinosis: Relief of symptoms and fever and a reduction of eosinophilia have followed the use of MINTEZOL during the invasion stage of the disease.Thiabendazole is usually inappropriate as first line therapy for enterobiasis (pinworm). However, when enterobiasis occurs with any of the conditions listed above, additional therapy is not required for most patients. MINTEZOL should be used only in the following infestations when more specific therapy is not available or cannot be used or when further therapy with a second agent is desirable: Uncinariasis (hookworm: Necator americanus and Ancylostoma duodenale); Trichuriasis (whipworm); Ascariasis (large roundworm). Launch Date1967 |
Cmax
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
5 μg/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7050189/ |
25 mg/kg single, oral dose: 25 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
THIABENDAZOLE serum | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
AUC
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
0.9 μg × min/mL EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7050189/ |
25 mg/kg single, oral dose: 25 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
THIABENDAZOLE serum | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
T1/2
| Value | Dose | Co-administered | Analyte | Population |
|---|---|---|---|---|
1.17 h EXPERIMENT https://pubmed.ncbi.nlm.nih.gov/7050189/ |
25 mg/kg single, oral dose: 25 mg/kg route of administration: Oral experiment type: SINGLE co-administered: |
THIABENDAZOLE serum | Homo sapiens population: UNHEALTHY age: ADULT sex: FEMALE food status: UNKNOWN |
Doses
| Dose | Population | Adverse events |
|---|---|---|
25 mg/kg 2 times / day steady, oral Recommended Dose: 25 mg/kg, 2 times / day Route: oral Route: steady Dose: 25 mg/kg, 2 times / day Sources: |
unhealthy, adult |
Other AEs: Asthenia, Epigastralgia... Other AEs: Asthenia (3 patients) Sources: Epigastralgia (1 patient) Disorientation (1 patient) |
AEs
| AE | Significance | Dose | Population |
|---|---|---|---|
| Disorientation | 1 patient | 25 mg/kg 2 times / day steady, oral Recommended Dose: 25 mg/kg, 2 times / day Route: oral Route: steady Dose: 25 mg/kg, 2 times / day Sources: |
unhealthy, adult |
| Epigastralgia | 1 patient | 25 mg/kg 2 times / day steady, oral Recommended Dose: 25 mg/kg, 2 times / day Route: oral Route: steady Dose: 25 mg/kg, 2 times / day Sources: |
unhealthy, adult |
| Asthenia | 3 patients | 25 mg/kg 2 times / day steady, oral Recommended Dose: 25 mg/kg, 2 times / day Route: oral Route: steady Dose: 25 mg/kg, 2 times / day Sources: |
unhealthy, adult |
Overview
| CYP3A4 | CYP2C9 | CYP2D6 | hERG |
|---|---|---|---|
OverviewOther
| Other Inhibitor | Other Substrate | Other Inducer |
|---|---|---|
Drug as perpetrator
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| no | ||||
| yes [Ki 1.54 uM] | ||||
Sources: https://pubmed.ncbi.nlm.nih.gov/11226373/ |
yes | |||
Page: 1.0 |
yes |
Drug as victim
| Target | Modality | Activity | Metabolite | Clinical evidence |
|---|---|---|---|---|
| yes |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Fast and easy multiresidue method employing acetonitrile extraction/partitioning and "dispersive solid-phase extraction" for the determination of pesticide residues in produce. | 2003-05-02 |
|
| Severe drug rashes in three siblings simultaneously. | 2003-05 |
|
| [Toxocariasis: clinical and laboratory features in 54 patients]. | 2003-05 |
|
| Fission yeast Rad26 responds to DNA damage independently of Rad3. | 2003-04-03 |
|
| Application of GRAM and TLD to the resolution and quantitation of real complex multicomponent mixtures by fluorescence spectroscopy. | 2003-04 |
|
| Treatment of cutaneous larva migrans and Toxocara infection. | 2003-04 |
|
| [A case of parasitism by Rhabditis sp in a child from Goiânia, Goiás, Brazil]. | 2003-03-08 |
|
| A more selective medium for Culicinomyces clavisporus. | 2003-03 |
|
| Simple and rapid determination of thiabendazole, imazalil, and o-phenylphenol in citrus fruit using flow-injection electrospray ionization tandem mass spectrometry. | 2003-02-12 |
|
| [Strongyloidiasis]. | 2003-02 |
|
| Antifungal agents of use in animal health--chemical, biochemical and pharmacological aspects. | 2003-02 |
|
| Ion trap tandem mass spectrometric identification of thiabendazole phototransformation products on titanium dioxide. | 2003-01-10 |
|
| A new role for the transcriptional corepressor SIN3; regulation of centromeres. | 2003-01-08 |
|
| [Selective vs. mass treatment with antihelminthic drugs: experience in two hyperendemic communities]. | 2003-01 |
|
| Photomutagenicity of thiabendazole, a postharvest fungicide, in bacterial assays. | 2003 |
|
| Methods for generation of monoclonal antibodies to the very small drug hapten, 5-benzimidazolecarboxylic acid. | 2002-12-20 |
|
| Oxidative, heat and anthelminthic stress responses in four species of Trichinella: comparative study. | 2002-12-01 |
|
| Pesticide residues in biological waste. | 2002-12 |
|
| Development and validation of a liquid chromatographic-electrospray tandem mass spectrometric multiresidue method for anthelmintics in milk. | 2002-11-08 |
|
| Bud morphogenesis and the actin and microtubule cytoskeletons during budding in the corn smut fungus, Ustilago maydis. | 2002-11 |
|
| Characterization of a Schizosaccharomyces pombe strain deleted for a sequence homologue of the human damaged DNA binding 1 (DDB1) gene. | 2002-10-25 |
|
| The effects of stage-specific selection on the development of benzimidazole resistance in Haemonchus contortus in sheep. | 2002-10-16 |
|
| Massive infestation of cutanea larva migrans. | 2002-10 |
|
| Cytokinetic actomyosin ring formation and septation in fission yeast are dependent on the full recruitment of the polo-like kinase Plo1 to the spindle pole body and a functional spindle assembly checkpoint. | 2002-09-15 |
|
| Active ammonia excretion across the gills of the green shore crab Carcinus maenas: participation of Na(+)/K(+)-ATPase, V-type H(+)-ATPase and functional microtubules. | 2002-09 |
|
| Analysis and partial reversal of multidrug resistance to anthelmintics due to P-glycoprotein in Haemonchus contortus eggs using Lens culinaris lectin. | 2002-09 |
|
| The comet assay with 8 mouse organs: results with 39 currently used food additives. | 2002-08-26 |
|
| [Disseminated strongyloidiasis, a rare cause of multiple organ failure]. | 2002-08-10 |
|
| Loeffler's syndrome and cutaneous larva migrans: a rare association. | 2002-08 |
|
| Opinion on the diagnosis and treatment of human trichinellosis. | 2002-08 |
|
| Cloning, production and characterisation of a recombinant Cu/Zn superoxide dismutase from Taenia solium. | 2002-08 |
|
| Induction of aneuploidy in male mouse germ cells detected by the sperm-FISH assay: a review of the present data base. | 2002-07-25 |
|
| Hyperinfective strongyloidiasis in the medical ward: review of 27 cases in 5 years. | 2002-07 |
|
| [Test treatment with antiparasitic agents for eosinophilia?]. | 2002-07 |
|
| Validation of a method for the determination of multiclass pesticide residues in fruit juices by liquid chromatography/tandem mass spectrometry after extraction by matrix solid-phase dispersion. | 2002-06-27 |
|
| [A case of toxocariasis with eosinophil-rich pleural effusion]. | 2002-06 |
|
| [DNA damage in female workers exposed to pesticides in banana plantations at Limón, Costa Rica]. | 2002-06 |
|
| Yeast RSC function is required for organization of the cellular cytoskeleton via an alternative PKC1 pathway. | 2002-06 |
|
| Thiabendazole for the prophylaxis of strongyloidiasis in immunosuppressed patients with hematological diseases: a randomized double-blind placebo-controlled study. | 2002-06 |
|
| Anthelmintics: a review. | 2002-04-20 |
|
| Residue uptake and storage responses of Tarocco blood oranges after preharvest thiabendazole spray and postharvest heat treatment. | 2002-04-10 |
|
| The p21-activated kinase, Shk1, is required for proper regulation of microtubule dynamics in the fission yeast, Schizosaccharomyces pombe. | 2002-04 |
|
| Analysis of thiabendazole and procymidone in fruits and vegetables by capillary electrophoresis-electrospray mass spectrometry. | 2002-03-08 |
|
| Treatment failure in intestinal strongyloidiasis: an indicator of HTLV-I infection. | 2002-03 |
|
| Human strongyloidiasis in AIDS era: its zoonotic importance. | 2002-03 |
|
| Estimation of concentrations of antifungal agents allowed as food additives in foods and their daily intake based on official inspection results in Japan in fiscal year 1998. | 2002-02 |
|
| Evaluation of certain veterinary drug residues in food. | 2002 |
|
| Ecchymoses: an unusual manifestation of toxocariasis in children. | 2001-12 |
|
| [Toxocariasis]. | 2001-12 |
|
| Parasitic infections of the intestine. | 2001-10 |
Patents
Sample Use Guides
The recommended maximum daily dose of MINTEZOL ((Thiabendazole) is 3 grams. MINTEZOL should be given after meals if possible. Tablets MINTEZOL should be chewed before swallowing. Dietary restriction, complementary medications and cleansing enemas are not needed. The usual dosage schedule for all conditions is two doses per day. The dosage is determined by the patient's weight.
Route of Administration:
Oral
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:36:40 GMT 2025
by
admin
on
Mon Mar 31 17:36:40 GMT 2025
|
| Record UNII |
N1Q45E87DT
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Official Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Brand Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WHO-ATC |
P02CA02
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
CFR |
21 CFR 520.2380C
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
CFR |
21 CFR 520.2380F
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
LIVERTOX |
NBK548194
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
WHO-ATC |
D01AC06
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
WHO-VATC |
QP52AC10
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
CFR |
21 CFR 520.2380A
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
CFR |
21 CFR 520.2380D
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
CFR |
21 CFR 558.600
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
NDF-RT |
N0000175481
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
EPA PESTICIDE CODE |
60101
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
WHO-VATC |
QD01AC06
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
CFR |
21 CFR 520.2380E
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
CFR |
21 CFR 520.2380B
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
CFR |
21 CFR 520.2380
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
CFR |
21 CFR 556.730
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
CFR |
21 CFR 524.1484G
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
||
|
NCI_THESAURUS |
C250
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
205-725-8
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
1655000
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
1436
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
C873
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
THIABENDAZOLE
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | Description: A white to almost white powder; odourless or almost odourless. Solubility: Practically insoluble in water; soluble in 150 parts of ethanol (~750 g/l) TS; slightly soluble in ether R. Category: Anthelmintic. Storage: Tiabendazole should be kept in a well-closed container. Definition: Tiabendazole contains not less than 98.0% and not more than 101.0% of C10H7N3S, calculated with reference to the dried substance. | ||
|
N1Q45E87DT
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
SUB10996MIG
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
90507
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
525040
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
TIABENDAZOLE
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
D013827
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
100000082153
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
N1Q45E87DT
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
45979
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
thiabendazole
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
DTXSID0021337
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
m10710
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | Merck Index | ||
|
CHEMBL625
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
2621
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
148-79-8
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
10450
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | RxNorm | ||
|
7304
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
2027
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
5430
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY | |||
|
DB00730
Created by
admin on Mon Mar 31 17:36:40 GMT 2025 , Edited by admin on Mon Mar 31 17:36:40 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
IMPURITY -> PARENT |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |