Oxazinanes
TARGETMOL CHEMICALS INC OLOPATADINE HYDROCHLORID 100MG
Also available in 5 mg 10 mg 25 mg 50 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Olopatadine hydrochloride (ALO4943A) is an antihistamine with mast-cell stabilizing properties used as eye drops in the treatment of ALLERGIC CONJUNCTIVITIS. purity: 99%
c1ccc(Cl)cc1Cl | 5g | 552761470](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502695750.jpg-250.jpg)
eMolecules 133773-29-2 | (R)-1-(2,4-Dichlorophenyl)ethanamine | Ambeed | MFCD06761788 | 190.070 | C8H9Cl2N | 95.000 | C[C@@H](N)c1ccc(Cl)cc1Cl | 5g | 552761470
(R)-1-(2,4-Dichlorophenyl)ethanamine | Ambeed | 133773-29-2 | MFCD06761788 | 190.070 | C8H9Cl2N | 95.000 | C[C@@H](N)c1ccc(Cl)cc1Cl | 5g | 552761470
TARGETMOL CHEMICALS INC RESMINOSTAT HYDROCHLORID 10MG
Also available in 1 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Resminostat hydrochloride (RAS2410 hydrochloride) is an effective inhibitor of HDAC1/HDAC3/HDAC6 (IC50 42.5/50.1/71.8 nM) respectively and shows less potent activities against HDAC8 (IC50 877 nM). purity: 99%
Cayman Chemical GW 3965 hydrochloride
An orally-active agonist of LXRα and LXRβ, activating the human isoforms with EC50 values of 190 and 30 nM, respectively; alters LXR-regulated gene expression in mice and rats, affecting pathways related to glucose and lipid metabolism
Cayman Chemical HA1077 hydrochloride
A potent inhibitor of ROCK2, PRK-2, MSK1, and MAPKAP-K1b with IC50 values of 1.9, 4, 5, and 15 µM, respectively; has been shown to reduce blood vessel constriction, decreases pulmonary arterial pressure, inhibit tumor angiogenesis, and improve insulin signaling in a diabetic rat model; drug forms are marketed for the treatment of pulmonary arterial hypertension and stable angina
TARGETMOL CHEMICALS INC QNZ 10MG
Also available in 1 mg 2 mg 5 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. QNZ (EVP4593) (EVP4593) is an effective inhibitor of NF-(kappa)B activation and TNF-(alpha) production. The IC50 of QNZ for NF-(kappa)B and TNF-(alpha) is11 nM and 7 nM respectively. purity: 99%
TARGETMOL CHEMICALS INC FLUPAROXAN HYDROCHLORIDE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Fluparoxan hydrochloride is a highly selective and potent (alpha)2-adrenoceptor antagonist for the prevention amelioration or treatment of neurodevelopmental disorders and neurodegenerative diseases. purity: 99%
TARGETMOL CHEMICALS INC VESAMICOL HYDROCHLORIDE 5MG
Also available in 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Vesamicol hydrochloride ((±)-AH5183 hydrochloride) is a acetylcholine transport inhibitor. purity: 98%
Medchemexpress LLC SSD114 hydrochloride | 2319790-02-6 | MFCD31619246 | 99.1% | 387.83 g/mol | C18H21ClF3N3O | 1 ML
SSD114 hydrochloride is a research-grade small molecule described as a novel GABAB receptor positive allosteric modulator for in vitro and preclinical studies.
- Research use only; not for human therapeutic use.
- Supplied as a 10 mM solution in DMSO, 1 mL vial.
- Also available as solid material in multiple weight sizes for formulation or dosing.
- High purity (≈99.1%), CAS 2319790-02-6, molecular weight 387.83 g/mol.
- Soluble in DMSO (≈130 mg/mL); limited water solubility.
- Store sealed, away from moisture; in solvent, keep at -80°C for long-term stability.
Sigma Aldrich Fine Chemicals Biosciences Leupeptin hydrochloride mi25MG
Leupeptin hydrochloride mi25MG
Medchemexpress LLC Ipatasertib dihydrochloride | 1396257-94-5 | 99.2% | 530.92 | 10 MG
Ipatasertib dihydrochloride is a highly selective and ATP-competitive pan-Akt inhibitor with IC50 values of 5 nM for Akt1, 18 nM for Akt2, and 8 nM for Akt3. It shows high selectivity for Akt1 over closely related kinases like PKA and p70S6K. In vivo, it is effective in xenograft models where Akt is activated due to genetic alterations, achieving tumor growth delay, stasis, or regression.
- Highly selective and ATP-competitive pan-Akt inhibitor
- Has IC50 values of 5 nM for Akt1, 18 nM for Akt2, and 8 nM for Akt3
- Shows over 600-fold selectivity for Akt1 against PKA, and 100-fold against p70S6K
- Effective in xenograft models where Akt is activated
- Achieves tumor growth delay, stasis, or regression in vivo
- Well tolerated in immunocompromised mice at therapeutic doses
- Enhances tumor growth inhibition in combination therapies
eMolecules Combi-Blocks 5-Aminopyridine-2-carboxamide 5g 205381682 AN-3936 98.000 145255-19-2 MFCD09879701 137.142 C6H7N3O
Combi-Blocks 5-Aminopyridine-2-carboxamide 5g 205381682 AN-3936 98.000 145255-19-2 MFCD09879701 137.142 C6H7N3O
Medchemexpress LLC Sapropterin dihydrochloride | 69056-38-8 | MFCD00891665 | 314.17 | C9H17Cl2N5O3 | 10 MG
Sapropterin dihydrochloride is the dihydrochloride salt of sapropterin ((6R)-BH4), supplied for research use as a PAH cofactor and analytical standard for studies of phenylketonuria and phenylalanine metabolism. It is provided as a solid and is intended for in vitro and analytical applications.
- Dihydrochloride salt form for improved handling and stability.
- Used as a cofactor in phenylalanine hydroxylase studies.
- Suitable for phenylketonuria and metabolic pathway research.
- Molecular formula C9H17Cl2N5O3; molecular weight 314.17 g/mol.
- Available in small research pack sizes suitable for assay and analytical work.
TARGETMOL CHEMICALS INC BESIFLOXACIN HYDROCHLORI 50MG
Also available in 5 mg 10 mg 25 mg 100 mg 200 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Besifloxacin Hydrochloride (BOL-303224-A) is a fourth-generation fluoroquinolone antibiotic. purity: 99%
TARGETMOL CHEMICALS INC A 77636 HYDROCHLORIDE 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. A 77636 hydrochloride is a potent orally active selective and long acting dopamine D1 receptor agonist (pKi=7.40; Ki=39.8 nM). A 77636 hydrochloride shows antiparkinsonian activity. A 77636 hydrochloride is functionally inactive at dopamine D2 receptor. purity: 99%