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Filtered Search Results
Medchemexpress LLC FAM49B (190-198) mouse | 1588388-60-6 | 1042.20 | 10 MG
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FAM49B (190-198) mouse is a peptide fragment of FAM49B. FAM49B is a mitochondria-localized protein that regulates mitochondrial fission, function and integrity, and tumor progression. It also acts as a negative regulator in T cell activation by repressing GTPase Rac activity and modulating cytoskeleton reorganization.
- Regulates mitochondrial fission
- Involved in mitochondrial function and integrity
- Contributes to tumor progression
- Acts as a negative regulator in T cell activation
- Represses GTPase Rac activity
- Modulates cytoskeleton reorganization
- Soluble in DMSO at 50 mg/mL
- Store as powder at -80°C for 2 years or -20°C for 1 year in sealed, moisture-free conditions
- Store in solvent at -80°C for 6 months or -20°C for 1 month in sealed, moisture-free conditions
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eMolecules Pharmablock 3-(tert-butoxycarbonylamino)tetrahydrofuran-3-carboxylic acid 250mg 551075652 PB05452 0 000 869785-31-9 MFCD04115501 231 248 C10H17NO5
Pharmablock 3-(tert-butoxycarbonylamino)tetrahydrofuran-3-carboxylic acid 250mg 551075652 PB05452 0 000 869785-31-9 MFCD04115501 231 248 C10H17NO5
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![Apexbio Technology LLC Cytochrome P450 CYP1B1 (190-198) [Homo sapiens] 5mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000096433.png-250.jpg)
Apexbio Technology LLC Cytochrome P450 CYP1B1 (190-198) [Homo sapiens] 5mg
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Cytochrome P450 CYP1B1 190-198 is a tumor-associated antigen peptide derived from CYP1B1 It is designed to induce HLA-A2-restricted T-cell responses against the CYP1B1(190-198) epitope thereby promoting tumor-specific cytotoxic immune responses Cytochrome P450 CYP1B1 190-198 exerts its biological activity primarily through antigen-specific activation of CD8 T cells In HLA-A2 transgenic mouse models this peptide delivered via plasmid DNA and poly(lactide-co-glycolide) microparticles demonstrates the ability to elicit CYP1B1 peptide-specific T-cell immunity Based on these pharmacological properties Cytochrome P450 CYP1B1 190-198 holds research potential in cancer immunotherapy and studies of tumor-specific cytotoxic T-cell responses
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![eMolecules AstaTech / 56-DICHLORO-2-(METHYLTHIO)-1H-BENZO[D]IMIDAZOLE / 0.25g / 386072812 / W17341 / 95.000 / 20076-54-4 / MFCD00662340 / 233.110 / C8H6Cl2N2S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502453721.PNG-250.jpg)
eMolecules AstaTech / 56-DICHLORO-2-(METHYLTHIO)-1H-BENZO[D]IMIDAZOLE / 0.25g / 386072812 / W17341 / 95.000 / 20076-54-4 / MFCD00662340 / 233.110 / C8H6Cl2N2S
AstaTech / 56-DICHLORO-2-(METHYLTHIO)-1H-BENZO[D]IMIDAZOLE / 0.25g / 386072812 / W17341 / 95.000 / 20076-54-4 / MFCD00662340 / 233.110 / C8H6Cl2N2S
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eMolecules Synthonix (S)-2-((tert-Butoxycarbonyl)amino)-3-methoxypropanoic acid 250mg 649434735 M38515 0 000 51293-47-1 MFCD00153314 219 237 C9H17NO5
Synthonix (S)-2-((tert-Butoxycarbonyl)amino)-3-methoxypropanoic acid 250mg 649434735 M38515 0 000 51293-47-1 MFCD00153314 219 237 C9H17NO5
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eMolecules Synthonix thiazol-5-ylmethyl N-[(1S 2S 4S)-1-benzyl-2-hydroxy-4-[[(2S)-2-[[(2-isopropylthiazol-4-yl)methyl-methyl-carbamoyl]amino]-3-methyl-butanoyl]amino]-5-phenyl-pentyl]carbamate 250mg 649428981 T71978 0 000 155213-67-5 MFCD00927142 720 950 C37H48N6O5S2
Synthonix thiazol-5-ylmethyl N-[(1S 2S 4S)-1-benzyl-2-hydroxy-4-[[(2S)-2-[[(2-isopropylthiazol-4-yl)methyl-methyl-carbamoyl]amino]-3-methyl-butanoyl]amino]-5-phenyl-pentyl]carbamate 250mg 649428981 T71978 0 000 155213-67-5 MFCD00927142 720 950 C37H48N6O5S2
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eMolecules Pharmablock [2-(tert-butoxycarbonylamino)-7-fluoro-1 3-benzothiazol-4-yl]boronic acid 25mg 601587323 PBU4948 0 000 2415163-55-0 312 120 C12H14BFN2O4S
Pharmablock [2-(tert-butoxycarbonylamino)-7-fluoro-1 3-benzothiazol-4-yl]boronic acid 25mg 601587323 PBU4948 0 000 2415163-55-0 312 120 C12H14BFN2O4S
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Medchemexpress LLC ML-298 10mg | 1426916-02-0 | 432.44 g·mol⁻1 | C22H23F3N4O2 | 10 MG
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ML-298 is a potent, selective small-molecule inhibitor of phospholipase D2 (PLD2) used in biochemical and cell-based research. It inhibits PLD2 with an IC50 of 355 nM, displays strong selectivity over PLD1, and has been shown to reduce invasive migration in U87-MG glioblastoma cells.
- Potent, selective PLD2 inhibition (IC50 355 nM).
- High selectivity over PLD1 (IC50 ≈ 20,000 nM).
- High purity suitable for research (≥98%).
- Supplied in research-scale quantities for in vitro studies.
- Stable as a powder under recommended storage conditions.
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eMolecules Ambeed / 2-Bromo-5-phenylthiazole / 100mg / 758385825 / A813345 / / 133311-51-0 / MFCD11109488 / 240.120 / C9H6BrNS
Ambeed / 2-Bromo-5-phenylthiazole / 100mg / 758385825 / A813345 / / 133311-51-0 / MFCD11109488 / 240.120 / C9H6BrNS
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Medchemexpress LLC Tert-butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate | 571188-59-5 | 99.97% | 278.36 | 500 G
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tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate is a drug intermediate used for the synthesis of various active compounds. It is intended for research use only and is not suitable for patient use. The compound appears as a solid with a white to yellow color.
- For research use only
- Solid appearance
- Color ranges from white to yellow
- Stored at 4°C, sealed, away from moisture and light
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Cell Signaling Technology TREM2 (E9U8L) Rabbit mAb (Amino-terminal Antigen) 20 ul
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TREM2 (E9U8L) Rabbit mAb (Amino-terminal Antigen) 20 ul
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![Medchemexpress LLC 1,2,4-triazolo[4,3-b]pyridazine, 3-[(2-methyl-2H-indazol-5-yl)thio]-6-(1-methyl-1H-pyrazol-4-yl)- | 1357072-61-7 | MFCD26960936 | 98.9% | 362.41 g/mol | C17H14N8S | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000288411.png-250.jpg)
Medchemexpress LLC 1,2,4-triazolo[4,3-b]pyridazine, 3-[(2-methyl-2H-indazol-5-yl)thio]-6-(1-methyl-1H-pyrazol-4-yl)- | 1357072-61-7 | MFCD26960936 | 98.9% | 362.41 g/mol | C17H14N8S | 10 MG
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c-Met inhibitor 1 is an orally active small-molecule inhibitor of the c-Met (HGFR) receptor tyrosine kinase with reported antitumor activity. It is supplied as a research-grade solid suitable for in vitro and in vivo pharmacology studies.
- Orally active c-Met kinase inhibitor for preclinical research.
- Demonstrated antitumor activity in multiple xenograft models.
- High purity, 98.9% by supplier analysis.
- Solid powder form suitable for formulation and dosing studies.
- Identifying data: CAS 1357072-61-7; formula C17H14N8S; MW 362.41 g/mol.
- Recommended storage: powder at -20°C for long-term, 4°C for short-term.
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Medchemexpress LLC (S,R,S)-AHPC-C10-NHBoc | 2412055-13-9 | 713.97 | 100 MG
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(S,R,S)-AHPC-C10-NHBoc is a synthesized E3 ligase ligand-linker conjugate that incorporates the (S,R,S)-AHPC based VHL ligand and a linker used for BET-Targeted PROTAC. This conjugate targets E3 ligase ligand-linker conjugates and is involved in the PROTAC pathway.
- Store powder at -20°C, sealed, away from moisture and light.
- For solutions, store at -80°C for 6 months or -20°C for 1 month, sealed and away from moisture and light.
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Medchemexpress LLC (S,R,S)-AHPC-C10-NHBoc | 2412055-13-9 | 713.97 | 50 MG
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(S,R,S)-AHPC-C10-NHBoc is a synthesized E3 ligase ligand-linker conjugate. It incorporates the (S,R,S)-AHPC based VHL ligand and a linker used for BET-Targeted PROTAC.
- Synthesized E3 ligase ligand-linker conjugate
- Incorporates (S,R,S)-AHPC based VHL ligand
- Used with a linker for BET-targeted PROTAC
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Medchemexpress LLC H-Met-OtBu.HCl | 91183-71-0 | 99.7% | 241.78 | 5 G
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H-Met-OtBu.HCl is a Methionine derivative for research use only. It is utilized as an ergogenic supplement, influencing the secretion of anabolic hormones, the supply of fuel during exercise, and mental performance in stressful tasks. It also helps prevent exercise-induced muscle damage.
- Impacts the secretion of anabolic hormones.
- Supports fuel supply during exercise.
- Enhances mental performance during stressful tasks.
- Prevents exercise-induced muscle damage.
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