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Filtered Search Results
U S PHARMACOPEIA MENAQUINONE VITAMIN K2
NC2594584 MENAQUINONE VITAMIN K2
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AMBEED 2 3-DIHYDROXYNAPHTHALENE 5 GR
NC3780149 2 3-DIHYDROXYNAPHTHALENE 5 GR
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TARGETMOL CHEMICALS INC BI-9564 25MG
502693963 BI-9564 25MG
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TARGETMOL CHEMICALS INC BI-7273 10MG
502693980 BI-7273 10MG
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ACCUSTANDARD INC 2-AMINONAPHTHALENE 1ML
NC3243393 2-AMINONAPHTHALENE 1ML
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MEDCHEMEXPRESS LLC MENAQUINONE-7 5MG
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501872393 MENAQUINONE-7 5MG
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GRAINGER INC 2-METHYL-1 4-NAPHTHOQUINONE 25
502781568 2-METHYL-1 4-NAPHTHOQUINONE 25
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Medchemexpress LLC 1-[(3,5-dichlorophenyl)sulfonyl]-N-[(4-fluorophenyl)methyl]-4-piperidinecarboxamide | 2227549-00-8 | >95.0% | 445.34 g·mol^-1 | C19H19Cl2FN2O3S | 100MG
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BI-01383298 is a small-molecule chemical probe that selectively inhibits the sodium-coupled citrate transporter SLC13A5 (NaCT). Developed by Boehringer Ingelheim and distributed by research suppliers, it is used in cellular studies to probe NaCT function. The compound is provided for laboratory research use only and is characterized by a defined molecular formula and molecular weight.
- Potent inhibitor of SLC13A5 with reported cellular IC50 values in the low nanomolar range (examples: 56 nM and 24 nM).
- High selectivity over related transporters, reported greater than 1,000-fold in some assays.
- Molecular weight approximately 445.3 g·mol^-1 and formula C19H19Cl2FN2O3S.
- Typical supplier-reported purity ≥95%, with some distributors listing higher specifications.
- Available as solid quantities and as a 10 mM solution in DMSO for cell-based assays.
- For research use only; not for human or clinical use.
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Medchemexpress LLC BI-765063 1mg | 1mg
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BI-765063 (OSE-172) is a humanized antibody expressed in CHO that targets SIRPa/CD172a BI-765063 contains an IgG4-type heavy chain and a hu -type light chain with a predicted molecular weight (MW) of 146 3 kDa The isotype control for BI-765063 can be referenced as Human IgG4 kappa Isotype Control (HY-P99003)
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eMolecules 82495-75-8 | Triphenyl((2-(trimethylsilyl)ethoxy)methyl)phosphonium chloride | Ambeed | MFCD00043159 | 429.010 | C24H30ClOPSi | 98.000 | [Cl-].C[Si](C)(C)CCOC[P+](c1ccccc1)(c1ccccc1)c1ccccc1 | 25g | 586454050
Triphenyl((2-(trimethylsilyl)ethoxy)methyl)phosphonium chloride | Ambeed | 82495-75-8 | MFCD00043159 | 429.010 | C24H30ClOPSi | 98.000 | [Cl-].C[Si](C)(C)CCOC[P+](c1ccccc1)(c1ccccc1)c1ccccc1 | 25g | 586454050
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Medchemexpress LLC 1-(3,5-dichlorophenyl)sulfonyl piperidin-4-yl (4-fluorophenyl)methylamino methanone | 2227549-00-8 | 99.3% | 444.0 g/mol | C19H19Cl2FN2O3S | 25MG
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BI01383298 is a chemical probe that potently and selectively inhibits the human sodium-citrate co-transporter SLC13A5 (NaCT). It exhibits low-nanomolar cellular potency and high selectivity, making it suitable for in vitro functional and mechanistic studies of citrate transport in human cells. Note: the compound shows no activity at mouse SLC13A5 and is therefore not recommended for mouse model studies.
- Potent inhibitor of human SLC13A5 with low-nanomolar cellular potency.
- High selectivity (>1,000-fold) over closely related transporters.
- Validated in HEK cells overexpressing SLC13A5 and HepG2 cells with endogenous expression.
- Irreversible, non-competitive inhibition mechanism useful for mechanistic studies.
- No activity against mouse SLC13A5; avoid mouse in vivo use.
- Reported high chemical purity suitable for research applications.
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eMolecules 2368881-70-1 | 2-Methylpyridin-5-ylmagnesium bromide, 0.25 M in THF | Synthonix196.330 | C6H6BrMgN | 0.000 | [Br-].Cc1ccc([Mg+])cn1 | 50ml | 702445941
2-Methylpyridin-5-ylmagnesium bromide, 0.25 M in THF | Synthonix | 2368881-70-1196.330 | C6H6BrMgN | 0.000 | [Br-].Cc1ccc([Mg+])cn1 | 50ml | 702445941
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AdipoGen N N-Bisphosphonomethylglycin
Chemical. CAS 2439-99-8. Formula C4H11NO8P2. MW 263.08. Synthetic. A glycine-phosphonic acid compound, negatively charged at neutral pH, with immunomodulatory and anti-diabetic properties. Enhances anti-B9-23 TCR-dependent T cell activation by modulating murine class II MHC I-Ag7-mediated B9-23 presentation on APCs. Daily administration of glyphosine is shown to delay the onset of diabetes in NOD mice. Herbicide. A plant growth regulator. Acts as a competitive inhibitor of phoshoenolpyruvate carboxylase in plants.
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eMolecules 479094-62-7 | Di-tert-butylmethylphosphine tetrafluoroborate | Synthonix | MFCD03840579 | 248.050 | C9H22BF4P | 95.000 | F[B-](F)(F)F.C[PH+](C(C)(C)C)C(C)(C)C | 10g | 719909080
Di-tert-butylmethylphosphine tetrafluoroborate | Synthonix | 479094-62-7 | MFCD03840579 | 248.050 | C9H22BF4P | 95.000 | F[B-](F)(F)F.C[PH+](C(C)(C)C)C(C)(C)C | 10g | 719909080
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Medchemexpress LLC 6-(5-methoxymethyl-pyridin-3-yl)-3,4-dihydro-2H-naphthyridine-1-carboxylic acid amide | 1633009-87-6 | 99.2% | 298.34 | C16H18N4O2 | 25 MG
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The compound is a small-molecule, highly selective aldosterone synthase (CYP11B2) inhibitor with nanomolar potency, used in biochemical and pharmacological research to probe aldosterone synthesis and CYP11B2-mediated pathways. It exhibits reported IC50 values of 2.1 nM for CYP11B2 and 310 nM for CYP11B1, and is supplied as a high-purity solid for laboratory studies.
- Highly selective aldosterone synthase inhibitor with nanomolar potency (CYP11B2 IC50 ≈ 2.1 nM).
- Reduced off-target activity against CYP11B1 (IC50 ≈ 310 nM).
- Molecular formula C16H18N4O2; molecular weight 298.34 g/mol.
- Purity 99.2% as reported by supplier.
- Supplied as a small solid quantity suitable for in vitro and in vivo research (e.g., 25 mg).
- Characterized in peer-reviewed pharmacology studies for selectivity and pharmacodynamics.
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