You Searched For: dibenzo[b,d]thiophene-4-carbaldehyde


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Catalog Number: (TCD0269-025G)
Supplier: TCI America
Description: CAS Number: 494-19-9
MDL Number: MFCD00005070
Molecular Formula: C14H13N
Molecular Weight: 195.27
Purity/Analysis Method: >97.0% (N)
Form: Crystal
Melting point (°C): 107

Supplier: TCI America
Description: CAS Number: 621-18-1
MDL Number: MFCD03844759
Molecular Formula: C14H10N2O4
Molecular Weight: 270.24
Purity/Analysis Method: >95.0% (HPLC,T)
Form: Crystal
Supplier: TCI America
Description: 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)dibenzofuran, Purity: >99.0%(GC)(T), CAS Number: 912824-85-2, Molecular Formula: C18H19BO3, MW: 294.16, Synonyms: Dibenzofuran-4-boronic Acid Pinacol Ester, Size: 5G

Supplier: Thermo Scientific Chemicals
Description: A tricyclic norepinephrine uptake inhibitor
Supplier: Bachem Americas
Description: Ramage resin is highly suitable for the preparation of peptide amides by the Fmoc-strategy and is recommended for C-terminal Phe, Tyr and Ile. Cleavage has been performed with 50 % TFA in CH₂Cl₂ or 95% aqueous TFA. Scavengers may be required. Tricyclic amide linker resin has been used for the synthesis of fluorogenic substrates for continuous assay of aminopeptidase P. Bachem additionally offers the Ramage amide linker (Q-2745) to be coupled to other types of carrier resin.

Supplier: Thermo Scientific Chemicals
Description: Iminodibenzyl 97%
Supplier: Thermo Scientific Chemicals
Description: Potent, selective muscarinic antagonist
Supplier: Thermo Scientific Chemicals
Description: Cytochrome P450 3A4 inducing anti-epileptic drug; ligand for the GABA-A receptor benzodiazepine modulatory site
Catalog Number: (TCE0414-005G)
Supplier: TCI America
Description: CAS Number: 25909-66-4
MDL Number: MFCD00144288
Molecular Formula: C20H22O6
Molecular Weight: 358.39
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Melting point (°C): 108

SDS


Supplier: Enzo Life Sciences
Description: Potent, selective and irreversible inhibitor of MAG lipase (IC50=8nM vs 4µM for FAAH). JZL-184-treated mice displayed a number of CB1-dependent behavioral effects including analgesia, hypothermia and hypomotility as well as increased levels of 2-arachidonoylglycerol in the brain ( approx. 8-fold, with no effect on anandamide levels). JZL-184 produces a rapid and sustained blockade of brain 2-AG hydrolase activity in mice. It blocks neuropathic pain and enhances retrograde endocannabinoid signaling.

Catalog Number: (CAAAAA11983-22)
Supplier: Thermo Scientific Chemicals
Description: MDL: MFCD00016576 Beilstein Registry No.: 2059467

Supplier: Thermo Scientific Chemicals
Description: Powder
Supplier: Enzo Life Sciences
Description: Potent, cell permeable, selective, and reversible inhibitor of c-Jun N-terminal kinase (JNK) (IC50=40nM for JNK-1 and JNK-2 and 90nM for JNK-3). The inhibition is competitive with respect to ATP. Exhibits over 300-fold greater selectivity for JNK as compared to ERK1 and p38. Inhibits the phosphorylation of c-Jun and blocks the expression of IL-2, IFN-γ, TNF-α, and COX-2. Blocks IL-1-induced accumulation of phospho-Jun, induction of c-Jun transcription and anti CD3-induced apoptosis of CD4+ CD8+ thymocytes.

Supplier: Thermo Scientific Chemicals
Description: A serotonin uptake inhibitor
Supplier: Thermo Scientific Chemicals
Description: Iminostilbene 97%
Supplier: Thermo Scientific Chemicals
Description: 10,11-Dihydrocarbamazepine 99%
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