Indanes
Ethos Biosciences Loeffler's Methylene Blue, 16oz, Ethos
Loeffler’s Methylene Blue is a staining solution designed for microbiology, cytology, and general laboratory applications. Commonly used as a simple stain, it provides rapid coloration of bacterial cells for clear visualization of morphology during microscopic evaluation. The formulation delivers consistent color intensity, making it ideal for routine diagnostic and teaching laboratories. It is also suitable for use as a counterstain in select staining procedures. Supplied in chemically compatible containers, Loeffler’s Methylene Blue is appropriate for clinical, research, and educational laboratory environments.
Medchemexpress LLC Methylene Blue | 61-73-4 | 95.1% | C16H18ClN3S | 500 MG
Methylene blue (Basic Blue 9) is an inhibitor of guanylyl cyclase (sGC), monoamine oxidase A (MAO-A), and NO synthase (NOS). It acts as a vasopressor and is commonly used as a dye in medical procedures. This REDOX cycling compound crosses the blood-brain barrier, inhibits Tau aggregation, and functions as a photosensitizer and redox agent, reducing cerebral edema, microglial activation, and neuroinflammation.
- Inhibits guanylyl cyclase (sGC), monoamine oxidase A (MAO-A), and NO synthase (NOS)
- Acts as a vasopressor and dye in medical procedures
- Reduces prepulse inhibition
- Functions as a REDOX cycling compound, crossing the blood-brain barrier
- Acts as a Tau aggregation inhibitor, photosensitizer, and redox agent
- Reduces cerebral edema, attenuates microglial activation, and decreases neuroinflammation
eMolecules Indan-1,6-diamine dihydrochloride | 2387535-17-1 | | 1g
J & W PharmLab LLC | Indan-1,6-diamine dihydrochloride | 1g | 491380145 | 20R1789S | 96.000 | 2387535-17-1 | | 221.130 | C9H14Cl2N2
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eMolecules 2-Bromo-1-indanol | 5400-80-6 | MFCD00003798 | 1g
Oakwood Chemical | 2-Bromo-1-indanol | 1g | 537664181 | 003061 | | 5400-80-6 | MFCD00003798 | 213.074 | C9H9BrO
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Medchemexpress LLC Phenothiazin-5-ium, 3,7-bis(dimethylamino)-, chloride, hydrate | 122965-43-9 | 100 G
Methylene blue hydrate is an inhibitor of guanylyl cyclase (sGC), monoamine oxidase A (MAO-A), and NO synthase (NOS). It acts as a vasopressor and is commonly used as a dye in various medical procedures. This compound influences the nitric oxide synthase/guanylate cyclase signaling pathway to decrease prepulse inhibition.
- Acts as a REDOX cycling compound
- Capable of crossing the blood-brain barrier
- Identified as a Tau aggregation inhibitor
- Reduces cerebral edema and attenuates microglial activation
- Lessens neuroinflammation
Apexbio Technology LLC MCC950 sodium(Synonyms: CP-456773 sodium, CRID3 sodium, MCC-950 sodium, MCC950 sodium salt), 10mg, CAS: 256373-96-3.
MCC950 sodium (CAS 256373-96-3) is a selective small-molecule inhibitor targeting the NOD-like receptor family protein 3 (NLRP3) inflammasome MCC950 sodium inhibits NLRP3 activation in murine bone marrow-derived macrophages (BMDMs) with an IC50 of 7 5 nM and demonstrates comparable selectivity and potency in human monocyte-derived macrophages (HMDMs) It specifically blocks both canonical and noncanonical activation pathways without affecting other inflammasomes such as AIM2 NLRC4 and NLRP1 Due to its selectivity MCC950 sodium is valuable in investigating NLRP3-associated inflammatory and autoimmune conditions
Medchemexpress LLC Phosphonic acid, P-(2-amino-2,3-dihydro-1H-inden-2-yl)-, hydrochloride (1:1) | 1416354-35-2 | MFCD23135861 | 98.4% | 249.63 g/mol | C9H13ClNO3P | 50 MG
2-Aminoindan-2-phosphonic acid hydrochloride is the hydrochloride salt of 2-aminoindan-2-phosphonic acid, a competitive phenylalanine ammonia-lyase (PAL) inhibitor used in biochemical assays and plant metabolism research. It is supplied as a solid of high purity (≈98.4%) with reported formula C9H13ClNO3P and molecular weight 249.63 g/mol; documentation such as a certificate of analysis and safety data sheet is available.
- High purity solid suitable for biochemical assays and research use.
- Acts as a competitive phenylalanine ammonia-lyase (PAL) inhibitor.
- Well characterized: formula C9H13ClNO3P, molecular weight 249.63 g/mol.
- Available in small-scale quantities for laboratory research.
- Certificate of analysis and safety data sheet available for quality and handling information.
Medchemexpress LLC 2-Aminoindan-2-phosphonic acid | 141120-17-4 | MFCD23701560 | 213.17 | 50 MG
2-Aminoindan-2-phosphonic acid is an inhibitor of phenylalanine ammonia-lyase (PAL). It reduces the biosynthesis and accumulation of total phenolic compounds in the suspension cell culture system of Cistanche.
- Inhibits PAL activity
- Decreases accumulation of total phenolic compounds
- Decreases accumulation of Echinacoside
- Decreases accumulation of Verbascoside
- Decreases accumulation of Cistanoside A
- Decreases accumulation of Tubuloside A
- Decreases accumulation of Salidroside
Medchemexpress LLC (1R,2R)-1-Aminoindan-2-ol | 163061-73-2 | 149.19 | 10 G
(1R,2R)-1-Aminoindan-2-ol is an isomer of (1S,2R)-1-Aminoindan-2-ol, suitable for use as a biological material or organic compound in life science research. It serves as a starting material for preparing an indene-based chiral auxiliary used in aldol reactions and for synthesizing oxazoline-alcohol ligands.
- Utilized as a biological material
- Used as an organic compound for life science research
- Starting material for indene-based chiral auxiliary in aldol reactions
- Synthesizes oxazoline-alcohol ligands
- Biochemical assay reagent
- Inhibitor
Medchemexpress LLC (1R,2R)-1-Aminoindan-2-ol | 163061-73-2 | 149.19 | 500 MG
(1R,2R)-1-Aminoindan-2-ol is an isomer of (1S,2R)-1-Aminoindan-2-ol. It can be utilized as a biological material or organic compound for life science research. This product can also serve as a starting material for preparing an indene-based chiral auxiliary used in aldol reactions, and in the synthesis of oxazoline-alcohol ligands.
- Utilized as a biological material
- Organic compound for life science research
- Starting material for preparing an indene-based chiral auxiliary used in aldol reactions
- Starting material in the synthesis of oxazoline-alcohol ligands