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Filtered Search Results
eMolecules 839712-12-8 | Medchem Express | Cariprazine | 5mg | 446264526 | HY-14763 | MFCD19443701 | 427.41 | C21H32Cl2N4O
Medchem Express | Cariprazine | 5mg | 446264526 | HY-14763 | 839712-12-8 | MFCD19443701 | 427.410 | C21H32Cl2N4O
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Sigma Aldrich Fine Chemicals Biosciences Neomycin sulfate United States Pharmacopeia (USP) Reference Standard | 1405-10-3 | 200MG
Neomycin sulfate United States Pharmacopeia (USP) Reference Standard | Mol Wt: 908.88 | 1405-10-3 | 200MG
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Research Products International Corp Puromycin Dihydrochloride, 25 Milligrams
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Puromycin Dihydrochloride is a potent antibiotic. It is an amino nucleoside antibiotic that mimics the 3'-end of aminoacyl-tRNA. It enters the ribosomal A site during translation, causing premature chain termination and inhibiting protein synthesis. Puromycin is incorporated into growing polypeptide chains, leading to the release of incomplete and nonfunctional peptides.
Widely used as a tool in cell biology to study protein synthesis and investigate translation processes. Its ability to terminate protein synthesis at the ribosome makes it valuable for various applications, including pulse-chase experiments and the analysis of nascent peptides. Puromycin resistance genes are often used as selectable markers in genetic engineering. Cells expressing the resistance gene can survive and proliferate in the presence of Puromycin, allowing for the selection of transfected or transduced cells.
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Research Products International Corp Timentin [Ticarcillin Disodium Salt/Potassium Cavulanate Mixture 15:1 Ratio], 5 Grams
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Timentin contains two antibiotics: ticarcillin (a penicillin) and clavulanate potassium (a beta-lactamase inhibitor). The combination of ticarcillin and clavulanate enhances the spectrum of antibacterial activity by protecting ticarcillin from degradation by certain bacterial enzymes.
Ticarcillin inhibits bacterial cell wall synthesis, disrupting the integrity of the bacterial cell wall and leading to bacterial cell lysis. Clavulanate potassium works by inhibiting beta-lactamases, enzymes produced by bacteria that can inactivate beta-lactam antibiotics, such as ticarcillin. This combination is effective against a broad spectrum of bacteria, including those producing beta-lactamases.
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Medchemexpress LLC HY-113328 1g Medchemexpress, Aminoadipic acid CAS:542-32-5 Purity:>98%
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Medchemexpress, HY-113328 1g Aminoadipic acid CAS:542-32-5 Aminoadipic acid is an intermediate in the metabolism of lysine and saccharopine. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-100522 1mg Medchemexpress, FMK 9a CAS:1955550-51-2 Purity:>98%
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Medchemexpress, HY-100522 1mg FMK 9a CAS:1955550-51-2 FMK 9a is an autophagin-1 inhibitor with IC 50 values of 80 and 73 μM in FRET and LRA assay. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Azido-peg4-val-cit-pab-oh | 2055024-64-9 | MFCD29918229 | 98.0% | 652.74 g/mol | C29H48N8O9 | 100 MG
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Azido-PEG4-Val-Cit-PAB-OH is a cleavable PEG-based linker used for assembling antibody-drug conjugates and other conjugates. It features an azide functional group for click chemistry and a protease-cleavable Val-Cit-PAB spacer that enables enzymatic payload release.
- cleavable PEG-based linker for ADC and conjugate synthesis.
- contains an azide group for CuAAC and SPAAC click reactions.
- protease-sensitive Val-Cit-PAB spacer enabling payload release.
- molecular weight 652.74 g/mol and formula C29H48N8O9.
- high purity (98.0%) with recommended storage conditions for powder and solution.
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Medchemexpress LLC HY-17362 1g Medchemexpress, Vancomycin (hydrochloride) CAS:1404-93-9 Purity:>98%
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Medchemexpress, HY-17362 1g Vancomycin (hydrochloride) CAS:1404-93-9 Vancomycin hydrochloride is an antibiotic for the treatment of bacterial infections. It acts by inhibiting the second stage of cell wall synthesis of susceptible bacteria. Vancomycin also alters the permeability of the cell membrane and selectively inhibits ribonucleic acid synthesis. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 303-97-9 | Medchem Express | Coenzyme Q9 | 1mg | 446256788 | HY-101415 | MFCD00056635 | 795.246 | C54H82O4
Ambeed | Methyl 4-(bromomethyl)-3-chlorobenzoate | 1g | 525079163 | A163410 | 74733-30-5 | MFCD10566565 | 263.520 | C9H8BrClO2
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Medchemexpress LLC HY-13238A 5mg Medchemexpress, Dolutegravir (sodium) CAS:1051375-19-9 Purity:>98%
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Medchemexpress, HY-13238A 5mg Dolutegravir (sodium) CAS:1051375-19-9 Dolutegravir sodium (S/GSK1349572 sodium) is a highly potent and orally bioavailable HIV integrase strand transfer inhibitor with an IC50 of 2.7 nM for HIV-1 integrase-catalyzed strand transfer. Dolutegravir sodium (S/GSK1349572 sodium) inhibits HIV-1 viral replication with an IC50 of 0.51 nM in peripheral blood mononuclear cells. Dolutegravir sodium (S/GSK1349572 sodium) retains a high potency against the HIV-1 Y143R, N155H, and G140S/Q148H mutants (EC50=3.6-5.8 nM). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC Recilisib (ON 01210) | 334969-03-8 | MFCD07366276 | 99.9% | 336.79 g/mol | C16H13ClO4S | 25 MG
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Recilisib is a small-molecule radioprotectant that activates PI3K and AKT signaling to protect hematopoietic progenitor cells from radiation-induced damage. It preserves colony-forming ability of bone marrow cells in vitro and enhances recovery of myeloid progenitors in vivo. Chemical properties include formula C16H13ClO4S and molecular weight 336.79 g/mol.
- Acts as a radioprotectant by activating PI3K and AKT signaling in cells.
- Protects bone marrow colony-forming units from radiation-induced depletion.
- Enhances recovery and differentiation of primitive myeloid progenitors in vivo.
- Solid, white to off-white form with DMSO solubility and established in vivo formulations.
- High purity (≈99.9%) suitable for research use.
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Medchemexpress LLC HY-107910 10mg Medchemexpress, Hyaluronidase CAS:37326-33-3 Purity:>98%
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Medchemexpress, HY-107910 10mg Hyaluronidase CAS:37326-33-3 Hyaluronidase (Hyaluronate 4-glycanohydrolase; Hyaluronoglucosaminidase) is a naturally occurring enzyme that depolymerizes hyaluronic acid by cleavage of glycosidic bonds and has been utilized in ophthalmic surgery. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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eMolecules 331963-29-2 | Medchem Express | I2906 | 100mg | 446271477 | HY-76293 | MFCD01128075 | 443.588 | C25H37N3O4
AbaChemScene | Ethyl (E)-3-morpholinoacrylate | 100mg | 410753097 | CS-0047053 | 81239-01-2 | MFCD28252204 | 185.223 | C9H15NO3
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Medchemexpress LLC HY-19776 50mg Medchemexpress, 3α-Aminocholestane CAS:2206-20-4 Purity:98%
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Medchemexpress,HY-19776 50mg 3α-Aminocholestane CAS:2206-20-4 Formula:C27H49N 3α-Aminocholestane is a selective SH2 domain-containing inositol-5′-phosphatase 1 (SHIP1) inhibitor with an IC50 of ~2.5 μM. Purity:98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC GSK3368715 | 1629013-22-4 | 99.4% | 10 MG
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GSK3368715 is an orally active, reversible type I protein arginine methyltransferases (PRMTs) inhibitor. It induces a shift in arginine methylation states, modifies exon usage, and exhibits strong anti-cancer activity, making it suitable for oncology research.
- Orally active and reversible inhibitor
- Inhibits type I protein arginine methyltransferases (PRMTs)
- Induces shifts in arginine methylation states
- Modifies exon usage
- Demonstrates strong anti-cancer activity
- Effective against a broad range of cancer cell lines
- Target: Histone Methyltransferase
- Pathway: Epigenetics
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