Temozolomide - Moligand™, ≥98%(HPLC) , DNA inhibitor, CAS No.85622-93-1, DNA inhibitor

CAS: 85622-93-1 Cat. No.: T127425 Formule: C6H6N6O2 Poids moléculaire: 194.15 Numéro CE: 630-358-9 PubChem CID: 5394
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%(HPLC)
Synonyms
4-methyl-5-oxo-2,3,4,6,8-pentazabicyclo[4.3.0]nona-2,7,9-triene-9-carboxamide | CCRG 81045 | NSC 362856 | TMZ | 3,4-Dihydro-3-methyl-4-oxoimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide | 8-Carbamoyl-3-methylimidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one | TZM
Storage
Store at 2-8°C,Argon charged
Shipped In
Wet ice
★
Taille
Allemagne (EU)
USA*
Prix
Qté
250mg
T127425-250mg
—
2 En stock
8,59€
500mg
T127425-500mg
—
3 En stock
9,46€
1g
T127425-1g
—
3 En stock
10,33€
5g
T127425-5g
—
2 En stock
31,15€
25g
T127425-25g
—
2 En stock
135,28€
100g
T127425-100g
—
2 En stock
520,56€
Enter a quantity for the sizes you want to add.
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Pourquoi cette qualité

Moligand™, ≥98%(HPLC) Moligand™ pour les flux de travail chromatographiques et analytiques sensibles nécessitant une interférence de ligne de base minimale.

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Stockage & expédition

Store at 2-8°C,Argon charged Expédition Wet ice. Consultez le COA spécifique au lot pour les spécifications exactes.

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Documents qualité

SDS, COA, fiche technique et fiche de spécifications disponibles au téléchargement. COA spécifique au lot accessible via la recherche par numéro de lot.

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Preuve documentaire

Cité dans 43 publications à comité de lecture couvrant la chromatographie, la synthèse organique et les réactions de couplage croisé.

Vue d’ensemble

Temozolomide is a DNA damage inducer.
An apoptosis inducer which causes arrest at the G2/M cell cycle checkpoint.

Spécifications

Synonymes
4-methyl-5-oxo-2,3,4,6,8-pentazabicyclo[4.3.0]nona-2,7,9-triene-9-carboxamide | CCRG 81045 | NSC 362856 | TMZ | 3,4-Dihydro-3-methyl-4-oxoimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide | 8-Carbamoyl-3-methylimidazo[5,1-d]-1,2,3,5-tetrazin-4(3H)-one | TZM
Spécifications et pureté
Moligand™, ≥98%(HPLC)
Mécanismes biochimiques et physiologiques
enzyme. Research has also been conducted to determine whether MGMT inhibitors such as O-6-benzylguanine might help to increase the efficacy of temozolomide. Furthermore, temozolomide has been implicated in causing arrest at the G2/M cell cycle checkpoint,
Conditions de stockage de stockage
Store at 2-8°C,Argon charged
Expédié en
Wet ice
Ce produit nécessite l'expédition en chaîne froide. Les services terrestres et autres services économiques ne sont pas disponibles.
Grade
Moligand™
Type d'action
INHIBITOR
Mécanisme d'action
DNA inhibitor
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureté
≥98%(HPLC)
Propriétés du produit
ALogP
-1.1
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/504750883
Sourires canoniques
CN1C(=O)N2C=NC(=C2N=N1)C(=O)N
IUPAC Name
3-methyl-4-oxoimidazo[5,1-d][1,2,3,5]tetrazine-8-carboxamide
InChIKey
BPEGJWRSRHCHSN-UHFFFAOYSA-N
INCHI
1S/C6H6N6O2/c1-11-6(14)12-2-8-3(4(7)13)5(12)9-10-11/h2H,1H3,(H2,7,13)
Isomères SMILES
CN1C(=O)N2C=NC(=C2N=N1)C(=O)N
WGK Allemagne
3
RTECS
NJ5927050
PubChem CID
5394
Poids moléculaire
194.15
Reaxy-Rn
5547136

Documentation

📋 Fiche de données de sécurité (FDS)

Document complet couvrant les dangers, la manipulation, le stockage et la conformité réglementaire.

<<<<<<< HEAD Télécharger la SDS → ======= Télécharger la SDS → >>>>>>> release248-p3

✅ Certificat d'analyse (COA)

Données qualité spécifiques au lot. Saisissez votre numéro de lot pour récupérer le COA exact.

Rechercher le COA →

📊 Fiche technique

Résumé de référence rapide des spécifications et applications du produit.

Voir la fiche technique →

🔬 Fiche de spécifications

Attributs de qualité complets et critères d'acceptation pour cette qualité.

Voir la fiche de spécifications →

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClasseImidazotetrazines
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentImidazotetrazines
Alternative Parents 2-heteroaryl carboxamides  Carbonylimidazoles  Tetrazines  N-substituted imidazoles  Vinylogous amides  Heteroaromatic compounds  Primary carboxylic acid amides  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Imidazotetrazine - 2-heteroaryl carboxamide - Imidazole-4-carbonyl group - N-substituted imidazole - Tetrazine - Azole - Imidazole - Heteroaromatic compound - Vinylogous amide - Carboxamide group - Primary carboxylic acid amide - Carboxylic acid derivative - Azacycle - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as imidazotetrazines. These are organic polycyclic compounds containing an imidazole ring fused to a tetrazine ring. Imidazole is 5-membered ring consisting of three carbon atoms, and two nitrogen centers at the 1- and 3-positions. Tetrazine is a six-membered aromatic heterocycle made up of four nitrogen atoms and a two carbon atoms.
External Descriptors monocarboxylic acid amide - triazene derivative - imidazotetrazine
Structure 3D
Modèle de structure chimique interactif





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ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
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HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
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ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
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AR Tclin Androgen Receptor (11781 Activities)
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CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
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DRD2 Tclin Dopamine D2 receptor (23596 Activities)
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GABRA1 Tclin GABA receptor alpha-1 subunit (399 Activities)
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MAOA Tclin Monoamine oxidase A (11911 Activities)
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CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
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DRD1 Tclin Dopamine D1 receptor (9720 Activities)
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DRD4 Tchem Dopamine D4 receptor (7907 Activities)
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ACHE Tclin Acetylcholinesterase (18204 Activities)
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PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
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HRH2 Tclin Histamine H2 receptor (5428 Activities)
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HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
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HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
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AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
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ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
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AGTR1 Tclin Type-1 angiotensin II receptor (5176 Activities)
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SLC6A4 Tclin Serotonin transporter (12625 Activities)
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CRHR1 Tclin Corticotropin releasing factor receptor 1 (2996 Activities)
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PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
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HRH1 Tclin Histamine H1 receptor (7573 Activities)
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OPRM1 Tclin Mu opioid receptor (19785 Activities)
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DRD3 Tclin Dopamine D3 receptor (14368 Activities)
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PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
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AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
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OPRD1 Tclin Delta opioid receptor (15096 Activities)
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OPRK1 Tclin Kappa opioid receptor (16155 Activities)
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HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GCGR Tclin Glucagon receptor (2563 Activities)
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SLC6A3 Tclin Dopamine transporter (10535 Activities)
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GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
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CACNA1C Tclin Voltage-gated L-type calcium channel alpha-1C subunit (766 Activities)
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PDE3A Tclin Phosphodiesterase 3A (3309 Activities)
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ESR2 Tclin Estrogen receptor beta (9272 Activities)
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SLC29A1 Tclin Equilibrative nucleoside transporter 1 (1711 Activities)
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ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)
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CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)
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Npy1r Neuropeptide Y receptor type 1 (8 Activities)
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Cckar Cholecystokinin A receptor (90 Activities)
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Mécanismes d'action
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37 results found

Lot NumberCertificate TypeDateArticle
I2602622I2602622Certificate of AnalysisAug 20, 2026 T127425
I2602621I2602621Certificate of AnalysisAug 20, 2026 T127425
I2602620I2602620Certificate of AnalysisAug 20, 2026 T127425
I2602619I2602619Certificate of AnalysisAug 20, 2026 T127425
J2227766J2227766Certificate of AnalysisMay 11, 2026 T127425
J2227749J2227749Certificate of AnalysisMay 11, 2026 T127425
J2227698J2227698Certificate of AnalysisMay 11, 2026 T127425
J2227652J2227652Certificate of AnalysisMay 11, 2026 T127425
J2227785J2227785Certificate of AnalysisMay 11, 2026 T127425
F2217267F2217267Certificate of AnalysisJan 26, 2026 T127425
A2408039A2408039Certificate of AnalysisOct 13, 2025 T127425
G2609053G2609053Certificate of AnalysisAug 15, 2025 T127425
G2609052G2609052Certificate of AnalysisAug 15, 2025 T127425
I2516494I2516494Certificate of AnalysisAug 15, 2025 T127425
I2516513I2516513Certificate of AnalysisAug 15, 2025 T127425
I2516514I2516514Certificate of AnalysisAug 15, 2025 T127425
I2516515I2516515Certificate of AnalysisAug 15, 2025 T127425
D2522521D2522521Certificate of AnalysisMar 20, 2025 T127425
D2507790D2507790Certificate of AnalysisMar 20, 2025 T127425
D2507784D2507784Certificate of AnalysisMar 20, 2025 T127425
D2507783D2507783Certificate of AnalysisMar 20, 2025 T127425
I2412042I2412042Certificate of AnalysisSep 21, 2024 T127425
I2412043I2412043Certificate of AnalysisSep 18, 2024 T127425
J2410762J2410762Certificate of AnalysisSep 04, 2024 T127425
J2410763J2410763Certificate of AnalysisSep 04, 2024 T127425
J2410764J2410764Certificate of AnalysisSep 04, 2024 T127425
B2508110B2508110Certificate of AnalysisSep 04, 2024 T127425
J2410761J2410761Certificate of AnalysisSep 04, 2024 T127425
D2408191D2408191Certificate of AnalysisMar 22, 2024 T127425
I1817142I1817142Certificate of AnalysisFeb 26, 2024 T127425
K2130076K2130076Certificate of AnalysisSep 15, 2023 T127425
K2130077K2130077Certificate of AnalysisSep 15, 2023 T127425
K2130078K2130078Certificate of AnalysisSep 15, 2023 T127425
K2130080K2130080Certificate of AnalysisSep 15, 2023 T127425
J2227772J2227772Certificate of AnalysisJul 21, 2022 T127425
D2409062D2409062Certificate of AnalysisJul 21, 2022 T127425
C2221050C2221050Certificate of AnalysisMar 24, 2022 T127425
Propriétés chimiques et physiques
SolubilitéSoluble in water (5 mg/ml at 25 °C), DMSO (39 mg/ml at 25 °C), and ethanol (<1 mg/ml at 25 °C).
SensibilitéHeat sensitive
Point de fusion (°C)206 °C(dec.)
Poids moléculaire194.150 g/mol
XLogP3-1.100
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count1
Exact Mass194.055 Da
Monoisotopic Mass194.055 Da
Topological Polar Surface Area106.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity315.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQ et articles
Citations of This Product
Calculateurs de solution
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