Organic phosphoric acids and derivatives
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Filtered Search Results
Medchemexpress LLC Diethyl 3-oxopentanedioate | 105-50-0 | ≥97.0% | 202.21 g·mol⁻¹ | C9H14O5 | 50 G
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Diethyl 3-oxopentanedioate (diethyl acetonedicarboxylate) is an organic biochemical reagent used as a building block in organic synthesis and in biochemical assay development. It is supplied for laboratory research applications.
- High purity (≥97.0%).
- Molecular formula C9H14O5; molecular weight 202.21 g·mol⁻¹.
- Suitable for organic synthesis and biochemical assay development.
- Available in multiple package sizes, including 50 g.
- Solutions available (10 mM in DMSO, 1 mL) for screening workflows.
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eMolecules 7784-09-0 | SILVER PHOSPHATE | AstaTech | MFCD00014148 | 418.574 | Ag3O4P | 95.000 | [Ag+].[Ag+].[Ag+].[O-]P([O-])([O-])=O | 10g | 449770267
SILVER PHOSPHATE | AstaTech | 7784-09-0 | MFCD00014148 | 418.574 | Ag3O4P | 95.000 | [Ag+].[Ag+].[Ag+].[O-]P([O-])([O-])=O | 10g | 449770267
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Apexbio Technology LLC KN-92 phosphate 1135280-28-2 200mg
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KN-92 phosphate is a small-molecule analog of the Ca2 /calmodulin-dependent kinase II (CaMKII) inhibitor KN-93 It is designed as an inactive control compound to distinguish CaMKII-specific effects in experimental settings KN-92 phosphate does not inhibit CaMKII activity and thus serves as a negative control for CaMKII inhibition studies Additionally KN-92 phosphate blocks certain voltage-gated potassium (Kv) channels such as Kv1 2 and Kv1 5 reducing steady-state current amplitudes upon depolarization Based on these pharmacological properties KN-92 phosphate holds research potential in investigating mechanisms underlying CaMKII-related signaling pathways and Kv channel functions
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eMolecules 220886-02-2 | 8,8-Bis((2-carboxyethoxy)methyl)-3,6-dioxo-1-phenyl-2,10-dioxa-4,7-diazatridecan-13-oic acid | Combi-Blocks | MFCD18252296 | 528.511 | C23H32N2O12 | 95.000 | OC(=O)CCOCC(COCCC(O)=O)(COCCC(O)=O)NC(=O)CNC(=O)OCc1ccccc1 | 1g | 537624453
8,8-Bis((2-carboxyethoxy)methyl)-3,6-dioxo-1-phenyl-2,10-dioxa-4,7-diazatridecan-13-oic acid | Combi-Blocks | 220886-02-2 | MFCD18252296 | 528.511 | C23H32N2O12 | 95.000 | OC(=O)CCOCC(COCCC(O)=O)(COCCC(O)=O)NC(=O)CNC(=O)OCc1ccccc1 | 1g | 537624453
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Medchemexpress LLC Dihexadecyl hydrogen 100mg
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Dihexadecyl hydrogen phosphateIt is an organic compound belonging to phospholipids It s often used as an emulsifier which means it helps mix two substances together that don t usually mix well such as oil and water Dihexadecyl hydrogen phosphateIt has several applications in the food industry especially in the production of processed foods where it improves texture and stability Additionally it has applications in the pharmaceutical industry where it can be used ain the generation of micelles liposomes and other types of artificial membranes
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Medchemexpress LLC Phosphoric acid, calcium salt (2:3) | 7758-87-4 | 98.0% | 1 G
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Tricalcium phosphate is a biological material and organic compound widely used in life science research. It is suitable for various laboratory applications.
- Widely used in life science research
- Suitable for biochemical assays
- Used as an organic compound
- Applies to biological materials
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Medchemexpress LLC Pamidronate disodium pentahydrate | 109552-15-0 | 98.0% | 1 ML
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Pamidronate disodium pentahydrate is a second-generation nitrogen-containing bisphosphonate supplied as a 10 mM solution. It inhibits bone loss by significantly inhibiting subchondral bone loss in early osteoarthritis, achieved by upregulating osteoprotegerin expression and inhibiting RANKL, MMP-9, and TLR-4 in cartilage. It also inhibits Wnt and β-catenin signaling and is applicable for research on osteoporosis and osteosarcoma.
- Inhibits the cell viability of osteosarcoma cells (POS, HMPOS, COS31) at concentrations ranging from 0.001-1000 μM over 72 hours, without cytotoxicity to fibroblasts.
- Improves bone structure and alleviates degenerative changes of cartilage.
- Exhibits a protective effect against osteoarthritis in rabbit models.
- Increases bone volume fraction (BV/TV), trabecular thickness (TbTh), and trabecular number (TbN).
- Reduces cartilage surface erosion and increases chondrocyte and matrix content.
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ALADDIN SCIENTIFIC CORPORATION Diethyl carbonateDEC, 500ml
Diethyl carbonate(DEC) 99%Cas-105-58-8
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eMolecules 1309446-14-7 | (S)-4-Hydroxy-2,6-bis(2,4,6-tricyclohexylphenyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide | MFCD26793807 | 5g
ChemScene | 3-Iodo-45-dimethyl-1H-pyrazole | 100mg | 712788136 | CS-0373254 | 1533443-11-6 | 222.029 | C5H7IN2
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Medchemexpress LLC Oligodeoxynucleotide ODN 2216 (CpG oligodeoxynucleotide) | 332437-00-0 | 97.9% | 6,432.00 Da | 10 MG
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ODN 2216 is a Class A CpG oligodeoxynucleotide that acts as a human-specific Toll-like receptor 9 (TLR9) ligand and research reagent. It elicits robust type I interferon responses from plasmacytoid dendritic cells, promotes dendritic cell cytokine production, and can indirectly stimulate IFN-γ production in peripheral blood mononuclear cells.
- Human-specific TLR9 agonist that induces type I interferons.
- Stimulates IFN-α and IFN-β production by plasmacytoid dendritic cells.
- Promotes IL-12 production by dendritic cells and indirect IFN-γ production in PBMCs.
- Sequence: d(G-sp-G-sp-G-G-G-A-C-G-A-T-C-G-T-C-G-sp-G-sp-G-sp-G-sp-G-sp-G).
- Molecular weight approximately 6,432 Da and purity ~97.9%.
- Supplied as a 10 mg package; store sealed and away from moisture (in solvent: -80°C up to 6 months, -20°C up to 1 month).
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Medchemexpress LLC KN-93 (phosphate) | 1913269-12-1 | C26H32ClN2O8PS | 25 MG
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KN-93 phosphate is a cell-permeable, reversible, and competitive inhibitor of calmodulin-dependent kinase type II (CaMKII) with a Ki of 370 nM. It induces G1 cell cycle arrest and apoptosis, and blocks cell growth stimulated by various growth factors in NIH 3T3 cells. This compound also inhibits H+, K+-ATPase activity and helps prevent increased LV developed pressure during action potential prolongation.
- Purity of 99.72%
- Solid, white to off-white appearance
- Soluble in DMSO (100 mg/mL) and H2O (50 mg/mL) with ultrasonication
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Medchemexpress LLC Diethyl pyrocarbonate | 1609-47-8 | 99.33% | 250 G
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Diethyl pyrocarbonate is a potent, orally active, non-specific chemical inhibitor of RNase. It has been useful in vitro as an agent relatively specific for binding to imidazole of histidine. It inhibits central chemosensitivity in rabbits and can modify Ser, Thr, His, and Tyr residues. It can be used for modeling.
- Potent, orally active, non-specific chemical inhibitor of RNase.
- Useful in vitro as an agent relatively specific for binding to imidazole of histidine.
- Inhibits central chemosensitivity in rabbits.
- Can modify Ser, Thr, His and Tyr residues.
- Can be used for modeling.
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eMolecules 13001-39-3 | 1,4-Bis(2-cyanostyryl)benzene | Toronto Research Chemicals | MFCD00631008 | 332.406 | C24H16N2N#Cc1ccccc1\C=C\c1ccc(\C=C\c2ccccc2C#N)cc1 | 500mg | 601590624
1,4-Bis(2-cyanostyryl)benzene | Toronto Research Chemicals | 13001-39-3 | MFCD00631008 | 332.406 | C24H16N2N#Cc1ccccc1\C=C\c1ccc(\C=C\c2ccccc2C#N)cc1 | 500mg | 601590624
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Medchemexpress LLC 3-pyridinecarboxylic acid, 6-[5-(ethoxycarbonyl)-2-thiazolyl]-, ethyl ester | 1821370-70-0 | MFCD31715412 | 99.9% | 306.34 g/mol | C14H14N2O4S | 50 MG
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Diethyl-pythiDC is a small-molecule inhibitor of collagen prolyl 4-hydroxylases (CP4Hs) supplied for research use. It is provided as a high-purity research chemical, available as a solid or as a ready-made 10 mM solution in DMSO, and is used in cellular and in vitro studies to probe CP4H activity and collagen biosynthesis.
- Inhibits collagen prolyl 4-hydroxylases (CP4Hs) for research applications.
- High purity, 99.9% as reported by the manufacturer.
- Molecular weight 306.34 g/mol and formula C14H14N2O4S.
- Available as solid or 10 mM solution in DMSO for convenience.
- Suitable for in vitro and cellular assays to study collagen synthesis.
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Apexbio Technology LLC Estramustine phosphate sodium 52205-73-9 10mg
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Estramustine phosphate sodium (CAS 52205-73-9) is an orally bioavailable small molecule that functions as an antimicrotubule agent Structurally related to estradiol it interacts with microtubule-associated proteins (MAPs) promoting microtubule disassembly and disrupting mitotic spindle formation This action interferes with mitosis ultimately leading to apoptotic cell death Widely studied in prostate cancer models estramustine phosphate sodium serves as a valuable tool for investigating mechanisms of cell cycle regulation mitotic arrest and apoptosis in oncological and cellular biology research settings
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