Pyrroles
eMolecules 23351-07-7 | 4-(1H-Pyrrol-1-yl)benzonitrile | Combi-Blocks | MFCD00085164 | 168.199 | C11H8N2 | 98.000 | N#Cc1ccc(cc1)-n1cccc1 | 1g | 205411941
4-(1H-Pyrrol-1-yl)benzonitrile | Combi-Blocks | 23351-07-7 | MFCD00085164 | 168.199 | C11H8N2 | 98.000 | N#Cc1ccc(cc1)-n1cccc1 | 1g | 205411941
eMolecules 1261851-55-1 | 4-DIFLUOROMETHOXY-3-FLUOROPHENYLACETIC ACID | AstaTech | MFCD18395038 | 220.147 | C9H7F3O3 | 95.000 | OC(=O)Cc1ccc(OC(F)F)c(F)c1 | 1g | 164730171
4-DIFLUOROMETHOXY-3-FLUOROPHENYLACETIC ACID | AstaTech | 1261851-55-1 | MFCD18395038 | 220.147 | C9H7F3O3 | 95.000 | OC(=O)Cc1ccc(OC(F)F)c(F)c1 | 1g | 164730171
eMolecules 212127-83-8 | 1-Boc-2,5-Dihydro-1H-pyrrole-3-boronic acid, pinacol ester | Combi-Blocks | MFCD10697918 | 295.190 | C15H26BNO4 | 97.000 | CC(C)(C)OC(=O)N1CC=C(C1)B1OC(C)(C)C(C)(C)O1 | 1g | 117529922
1-Boc-2,5-Dihydro-1H-pyrrole-3-boronic acid, pinacol ester | Combi-Blocks | 212127-83-8 | MFCD10697918 | 295.190 | C15H26BNO4 | 97.000 | CC(C)(C)OC(=O)N1CC=C(C1)B1OC(C)(C)C(C)(C)O1 | 1g | 117529922
eMolecules 93939-74-3 | Ambeed | (R)-2-Amino-2-(4-fluorophenyl)acetic acid | 250mg | 521395351 | A111711 | MFCD00042727 | 169.155 | C8H8FNO2
Ambeed | (R)-2-Amino-2-(4-fluorophenyl)acetic acid | 250mg | 521395351 | A111711 | 93939-74-3 | MFCD00042727 | 169.155 | C8H8FNO2
Selleck Chemical LLC Bromoenol lactone-E1878-100MG
Bromoenol lactone((6E)-Bromoenol lactone) is a selective irreversible potent inhibitor of calcium-independent phospholipase A2 (iPLA2 ) with an IC50 value of 7 M It prevents antigen-stimulated exocytosis in mast cells without hindering Ca2 influx
Medchemexpress LLC Almotriptan (malate) | 181183-52-8 | 99.5% | 25 MG
Almotriptan malate is an orally active, highly selective 5-HT1B/1D-receptor agonist. It is utilized in research for treating migraine, inducing intracranial vasoconstriction, suppressing vasoactive peptides from trigeminal nerve endings, and inhibiting nociceptive neurotransmission in the trigeminocervical complex. This compound shows low nanomolar affinity for 5-HT1B and 5-HT1D receptors.
- Highly selective 5-HT1B/1D-receptor agonist
- Induces intracranial vasoconstriction
- Suppresses vasoactive peptide release
- Inhibits nociceptive neurotransmission
- Exhibits low nanomolar affinity for 5-HT1B and 5-HT1D receptors
- Has a mild antiemetic effect
- Shows a slight, transient diuretic effect
Medchemexpress LLC Nemonoxacin malate | 951163-60-3 | 99.29% | 505.52 | 100 MG
Nemonoxacin malate is a nonfluorinated quinolone antibiotic with broad-spectrum activity against Gram-positive, Gram-negative, and atypical pathogens. It can inhibit drug-resistant *Streptococcus pneumoniae* and Methicillin-resistant *Staphylococcus aureus* and can be used for the research of community-acquired pneumonia.
- Nonfluorinated quinolone antibiotic.
- Broad-spectrum activity against Gram-positive, Gram-negative and atypical pathogens.
- Inhibits drug-resistant *Streptococcus pneumoniae* and Methicillin-resistant *Staphylococcus aureus*.
- Used for the research of community-acquired pneumonia.
- Antibacterial activity against *Chlamydia pneumoniae* with MIC90s of 0.06 μg/mL.
- Highly active against community-acquired MRSA (CA-MRSA) (MIC90: 0.5 and 0.06 μg/ml), and exerts limited activity against Ciprofloxacin-resistant MRSA (MIC90: 1 μg/ml), and Vancomycin-intermediate MRSA (MIC90: 2 μg/ml).
Medchemexpress LLC Clebopride malate | 57645-91-7 | 99.4% | 1 ML
Clebopride malate is an orally active dopamine receptor antagonist. It acts on dopamine D2 receptors and exhibits antiemetic and prokinetic effects. This compound is suitable for research into functional gastrointestinal disorders.
- Orally active dopamine receptor antagonist
- Acts on dopamine D2 receptors
- Possesses antiemetic effects
- Exhibits prokinetic effects
- Selectively binds to D2 dopamine receptors and α2 adrenergic receptors
Medchemexpress LLC (3S,5S)-atorvastatin | 501121-34-2 | MFCD09839951 | 95.0% | 558.64 g/mol | C33H35FN2O5 | 10 MG
(3S,5S)-atorvastatin is the inactive stereoisomer of atorvastatin provided for research use. It is reported to act as a pregnane X receptor (PXR) agonist and is used in pharmacology and metabolic-disease studies. Supplied as a high-purity solid for in vitro and analytical applications.
- Inactive enantiomer of atorvastatin
- Acts as pregnane X receptor (PXR) agonist
- Supplied with reported purity of 95.0%
- Available in a 10 mg quantity for laboratory use
- Suitable for in vitro and analytical research; not for human use
Medchemexpress LLC Atorvastatin calcium hydrate | 344423-98-9 | 99.8% | 605.71 | 250 MG
Atorvastatin calcium hydrate is a statin-class drug designed to lower blood cholesterol and triglyceride levels. It functions by inhibiting HMG-CoA reductase, an enzyme crucial for cholesterol production in the liver. This action helps reduce the risk of heart attack and stroke. It is intended for life science research applications.
- Lowers blood cholesterol levels
- Controls high levels of LDL cholesterol and triglycerides
- Reduces risk of heart attack and stroke
- Inhibits HMG-CoA reductase, an enzyme in the liver
- Intended for life science research
Medchemexpress LLC Atorvastatin hemicalcium salt | 134523-03-8 | 99.9% | 577.67 | 5 MG
Atorvastatin hemicalcium salt | 134523-03-8 | 99.9% | 577.67 | 5 MG
Medchemexpress LLC Massoia lactone | 54814-64-1 | 5 G
Massoia lactone is a coconut and creamy fragrant compound primarily isolated from *Cryptocarya massoy*. It is also a fragrant biosurfactant produced by the fungus *Aureobasidium pullulans*.
- Purity: 98.75%
- Molecular weight: 168.23
- Molecular formula: C10H16O2
- Appearance: Liquid
- Color: Light yellow to light brown
- Shipping: Room temperature in continental US (may vary elsewhere)
- Storage (pure form): -20°C for 3 years
- Storage (in solvent): -80°C for 6 months, -20°C for 1 month
- Solubility in DMSO: 200 mg/mL (requires ultrasonic)
- For research use only
Medchemexpress LLC Atorvastatin calcium salt trihydrate | 344423-98-9 | 99.8% | 605.71 | 1 G
Atorvastatin calcium salt trihydrate is a drug belonging to the statin class of drugs used to lower blood cholesterol levels. Atorvastatin calcium salt trihydrate has unique chemical properties that make it an effective tool in controlling high levels of low-density lipoprotein (LDL) cholesterol and triglycerides in the body, reducing the risk of heart attack and stroke. Atorvastatin calcium salt trihydrate works by inhibiting HMG-CoA reductase, the enzyme responsible for producing cholesterol in the liver.
- Lowers blood cholesterol levels.
- Controls high levels of low-density lipoprotein (LDL) cholesterol and triglycerides.
- Reduces the risk of heart attack and stroke.
- Works by inhibiting HMG-CoA reductase, the enzyme responsible for producing cholesterol in the liver.
- Can be used as a biochemical reagent for life science-related research.
Apexbio Technology LLC Pizotifen Malate 5189-11-7 10mM (in 1mL DMSO)
Pizotifen malate (CAS 5189-11-7) is a benzocycloheptane derivative that functions as a potent antagonist of serotonin (5-HT) receptors exhibiting high selectivity for this target class By inhibiting serotonergic neurotransmission Pizotifen malate is utilized in biomedical research to investigate the physiological and pharmacological roles of 5-HT pathways Its receptor blocking properties enable studies focused on serotonergic modulation migraine mechanisms and disorders associated with altered serotonin signaling
Medchemexpress LLC (-)-Corey lactone diol | 32233-40-2 | 172.18 | 1 G
(-)-Corey lactone diol is the reduced form of Corey aldehyde. It serves as a drug intermediate in the synthesis of Beraprost. This product is intended for research use only and is not sold to patients. It appears as a white to off-white solid.
- Reduced form of Corey aldehyde.
- Used as a drug intermediate for the synthesis of Beraprost.
- Exclusively for research purposes.
- Appears as a white to off-white solid.
- Powder storage: -20°C for 3 years; 4°C for 2 years.
- In solvent storage: -80°C for 6 months; -20°C for 1 month.