Thiazoles

Aobchem 5-Iodo-2-phenylthiazole | ≥97% | CAS 1000029-07-1 | C9H6INS | 5g

5-Iodo-2-phenylthiazole | ≥97% | CAS 1000029-07-1 | C9H6INS | 5g

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Aobchem 5-(4-Chlorophenyl)thiazol-2-amine | ≥97% | CAS 73040-66-1 | C9H7ClN2S | 1g

5-(4-Chlorophenyl)thiazol-2-amine | ≥97% | CAS 73040-66-1 | C9H7ClN2S | 1g

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Aobchem 5-(4-Chlorophenyl)thiazol-2-amine | ≥97% | CAS 73040-66-1 | C9H7ClN2S | 250mg

5-(4-Chlorophenyl)thiazol-2-amine | ≥97% | CAS 73040-66-1 | C9H7ClN2S | 250mg

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Aobchem Ethanone 1-(5-methyl-4-isoxazolyl)- | ≥95% | CAS 6497-21-8 | C6H7NO2 | 250mg

Ethanone 1-(5-methyl-4-isoxazolyl)- | ≥95% | CAS 6497-21-8 | C6H7NO2 | 250mg

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Aobchem 5-(4-Chlorophenyl)thiazol-2-amine | ≥97% | CAS 73040-66-1 | C9H7ClN2S | 5g

5-(4-Chlorophenyl)thiazol-2-amine | ≥97% | CAS 73040-66-1 | C9H7ClN2S | 5g

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Aobchem Ethanone 1-(5-methyl-4-isoxazolyl)- | ≥95% | CAS 6497-21-8 | C6H7NO2 | 500mg

Ethanone 1-(5-methyl-4-isoxazolyl)- | ≥95% | CAS 6497-21-8 | C6H7NO2 | 500mg

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Medchemexpress LLC TH-Z145 | 2260887-57-6 | C16H28O7P2 | 25 MG

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TH-Z145 is a lipophilic bisphosphonate that functions as an FPPS inhibitor with an IC50 of 210 nM. It has shown promising effects in preclinical studies, including strong prophylactic effects in pathogenic influenza models and inhibition of tumor growth in xenograft mouse models.

• Exhibits strong prophylactic effects in pathogenic influenza models
• Inhibits tumor growth and prolongs survival in B16-OVA xenograft mouse models
• Functions as an FPPS inhibitor with an IC50 of 210 nM
• Appears as an off-white to light yellow solid
• Soluble in DMSO at 100 mg/mL
• Not classified as a hazardous substance or mixture

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Medchemexpress LLC KN-93 hydrochloride | 1956426-56-4 | C26H30Cl2N2O4S | 25 MG

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KN-93 hydrochloride is a cell-permeable, reversible, and competitive inhibitor of calmodulin-dependent kinase type II (CaMKII) with a Ki of 370 nM. It is intended for research use only.

• Cell-permeable, reversible, and competitive CaMKII inhibitor
• Ki of 370 nM
• Arrests cells in G1 phase
• Blocks cell growth stimulated by basic fibroblast growth factor, platelet-derived growth factor-BB, and epidermal growth factor
• Inhibits H+, K+-ATPase activity
• Prevents increased LV developed pressure during action potential prolongation

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Apexbio Technology LLC KN-93 hydrochloride 1956426-56-4 5mg

KN-93 hydrochloride (CAS 1956426-56-4) is a selective inhibitor of Ca2 /calmodulin-dependent protein kinase II (CaMK II) binding competitively at the calmodulin site with a reported Ki of 0 37 M and an IC50 of 370 nM In isolated gastric parietal cells KN-93 suppresses acid secretion stimulated by carbachol and histamine with IC50 values of 0 15 M and 0 3 M respectively and inhibits mucin-stimulated aminopyrine uptake (IC50 0 6 M) Additionally KN-93 shows inhibitory activity against H /K -ATPase and directly blocks voltage-gated potassium (Kv) channels by promoting C-type inactivation KN-93 is widely used to probe CaMK II signaling and its downstream physiological effects in cellular and electrophysiological studies

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eMolecules​ 2227199-12-2 | tert-butyl cis-N-(4-amino-1-methyl-cyclohexyl)carbamate;hydrochloride | Pharmablock264.790 | C12H25ClN2O2 | 97.000 | Cl.CC(C)(C)OC(=O)N[C@]1(C)CC[C@H](N)CC1 | 25mg | 551094144

tert-butyl cis-N-(4-amino-1-methyl-cyclohexyl)carbamate;hydrochloride | Pharmablock | 2227199-12-2264.790 | C12H25ClN2O2 | 97.000 | Cl.CC(C)(C)OC(=O)N[C@]1(C)CC[C@H](N)CC1 | 25mg | 551094144

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eMolecules​ 101711-55-1 | 2-(tert-Butyldimethylsilyloxy)ethanamine | Combi-Blocks | MFCD18206132 | 175.347 | C8H21NOSi | 95.000 | CC(C)(C)[Si](C)(C)OCCN | 1g | 303351987

2-(tert-Butyldimethylsilyloxy)ethanamine | Combi-Blocks | 101711-55-1 | MFCD18206132 | 175.347 | C8H21NOSi | 95.000 | CC(C)(C)[Si](C)(C)OCCN | 1g | 303351987

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eMolecules​ 111769-26-7 | (R)-Tetrahydrofuran-3-amine | Accela ChemBio | MFCD08234424 | 87.122 | C4H9NO | 97.000 | N[C@@H]1CCOC1 | 10g | 778445413

(R)-Tetrahydrofuran-3-amine | Accela ChemBio | 111769-26-7 | MFCD08234424 | 87.122 | C4H9NO | 97.000 | N[C@@H]1CCOC1 | 10g | 778445413

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eMolecules​ 78269-85-9 | Teoc-OSu | Ambeed | MFCD02683467 | 259.333 | C10H17NO5Si | 97.000 | C[Si](C)(C)CCOC(=O)ON1C(=O)CCC1=O | 10g | 525085968

Teoc-OSu | Ambeed | 78269-85-9 | MFCD02683467 | 259.333 | C10H17NO5Si | 97.000 | C[Si](C)(C)CCOC(=O)ON1C(=O)CCC1=O | 10g | 525085968

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Medchemexpress LLC 1,3-oxazolidine-2-thione | 5840-81-3 | MFCD00125763 | ≥98.0% | 103.15 g/mol | C3H5NOS | 10 MG

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1,3-oxazolidine-2-thione (CAS 5840-81-3) is a small heterocyclic organosulfur compound supplied for laboratory research and reference use. It is typically a white to off-white solid with molecular formula C3H5NOS and molecular weight about 103.15 g/mol. The substance has been used in biological studies and is provided with specified purity for experimental applications.

• Small heterocyclic organosulfur compound
• White to off-white solid appearance
• Molecular formula C3H5NOS and molecular weight 103.15 g/mol
• Soluble in DMSO (common laboratory solvent)
• Supplied with reported purity ≥98.0%
• Intended for laboratory research and reference use only

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Medchemexpress LLC Met kinase-IN-2 | 2101241-90-9 | 98.4% | C33H27FN4O4 | 10MG

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MET kinase-IN-2 is a potent, selective, orally bioavailable inhibitor of the MET (c-Met/HGFR) receptor tyrosine kinase. It inhibits MET with an IC50 of 7.4 nM, shows antitumor activity in cell-based assays, and has reported activity against several additional kinases and tumor cell lines. Supplied as a solid research chemical for laboratory use.

• Potent MET kinase inhibition (IC50 = 7.4 nM).
• Orally bioavailable, enabling in vivo studies.
• Demonstrated antitumor activity in cell assays.
• Shows additional kinase activity at higher concentrations.
• High-purity solid suitable for research applications.

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