Naphthalenes
6-Hydroxy-1-naphthoic Acid 98.0+%, TCI America™
CAS: 2437-17-4 Molecular Formula: C11H8O3 Molecular Weight (g/mol): 188.18 MDL Number: MFCD00209983 InChI Key: JCJUKCIXTRWAQY-UHFFFAOYSA-N Synonym: 6-Hydroxy-1-naphthalenecarboxylic Acid PubChem CID: 5463800 IUPAC Name: 6-hydroxynaphthalene-1-carboxylic acid SMILES: OC(=O)C1=C2C=CC(O)=CC2=CC=C1
Medchemexpress LLC Tamsulosin (hydrochloride) | 106463-17-6 | 99.8% | 25 MG
Tamsulosin hydrochloride is an orally active antagonist of the α1-adrenergic receptor. It induces apoptosis and is used for research related to prostatic hyperplasia. It also attenuates abdominal aortic aneurysm growth and inhibits inflammation in animal models.
- Orally active α1-adrenergic receptor antagonist
- Induces apoptosis
- Used for research of prostatic hyperplasia
- Attenuates abdominal aortic aneurysm growth
- Inhibits inflammation in animal models
- Stable under recommended storage conditions
- White to off-white solid appearance
Medchemexpress LLC Tamsulosin hydrochloride | 106463-17-6 | 99.8% | 100 MG
Tamsulosin hydrochloride is an orally active antagonist of the α1-adrenergic receptor. It induces apoptosis and is used for the research of prostatic hyperplasia. Tamsulosin hydrochloride also attenuates abdominal aortic aneurysm growth and inhibits inflammation in animal models.
- Orally active α1-adrenergic receptor antagonist
- Induces apoptosis
- Used for prostatic hyperplasia research
- Attenuates abdominal aortic aneurysm growth
- Inhibits inflammation in animal models
- Molecular weight: 444.97
- Chemical formula: C20H29ClN2O5S
- Appearance: Solid
- Color: White to off-white
- Recommended storage: 4°C, sealed, away from moisture and light
- Solvent storage: -80°C for 6 months; -20°C for 1 month (sealed, away from moisture and light)
- Solubility in DMSO: 50 mg/mL (112.37 mM)
Medchemexpress LLC Tamsulosin (hydrochloride) | 106463-17-6 | 99.8% | 1 ML
Tamsulosin hydrochloride is an orally active antagonist of the α1-adrenergic receptor. It is used in the research of prostatic hyperplasia and has been shown to induce apoptosis and attenuate abdominal aortic aneurysm growth and inflammation in animal models.
- Exhibits intrinsic activity at human alpha1B adrenergic receptor (EC50 of 0.13 nM).
- Attenuates high glucose-induced injury in human glomerular endothelial cells.
- Influences ECM production and distribution, and cellular metabolism levels in ARPE 19 cells.
- Induces apoptosis and clusterin expression in NRP-152 cells.
Chemscene ChemScene | 6-Hydroxy-1-naphthoic acid | 10G | CS-W016818 | 0.98 | 2437-17-4| MFCD00209983 | 188.18
ChemScene | 6-Hydroxy-1-naphthoic acid | 10G | CS-W016818 | 0.98 | 2437-17-4| MFCD00209983 | 188.18
Chemscene ChemScene | 6-Hydroxy-1-naphthoic acid | 25G | CS-W016818 | 0.98 | 2437-17-4| MFCD00209983 | 188.18
ChemScene | 6-Hydroxy-1-naphthoic acid | 25G | CS-W016818 | 0.98 | 2437-17-4| MFCD00209983 | 188.18
Chemscene ChemScene | 6-Hydroxy-1-naphthoic acid | 5G | CS-W016818 | 0.98 | 2437-17-4| MFCD00209983 | 188.18
ChemScene | 6-Hydroxy-1-naphthoic acid | 5G | CS-W016818 | 0.98 | 2437-17-4| MFCD00209983 | 188.18
eMolecules Synthonix n-Decylzinc bromide 0.50 M in THF 25ml 627353619 D73284 160516-17-6 MFCD07698739 286.560 C10H21BrZn
Synthonix n-Decylzinc bromide 0.50 M in THF 25ml 627353619 D73284 160516-17-6 MFCD07698739 286.560 C10H21BrZn
eMolecules Synthonix n-Decylzinc bromide 0.50 M in THF 100ml 532652793 D73284 160516-17-6 MFCD07698739 286.560 C10H21BrZn
Synthonix n-Decylzinc bromide 0.50 M in THF 100ml 532652793 D73284 160516-17-6 MFCD07698739 286.560 C10H21BrZn
eMolecules Synthonix n-Decylzinc bromide 0.50 M in THF 50ml 532652792 D73284 160516-17-6 MFCD07698739 286.560 C10H21BrZn
Synthonix n-Decylzinc bromide 0.50 M in THF 50ml 532652792 D73284 160516-17-6 MFCD07698739 286.560 C10H21BrZn
AdipoGen Naphthol AS-E phosphate
Chemical. CAS 18228-17-6. Formula C17H13ClNO5P. MW 377.72. Synthetic. Histochemical substrate for alkaline phosphatases. Aldolase inhibitor. Small molecule inhibitor. Anticancer compound that directly targets the KIX domain of CBP, resulting in a disrupted CREB-CBP complex, inhibited CREB-target gene induction and inhibited IL-1beta-mediated angiogenic activity in cancer cell lines. Inhibits activity of transcription factor Myb by blocking interaction with KIX domain of coactivator p300 in human leukemia cells. Interferes with the Myb–KIX interaction in vitro and inhibits Myb activity in vivo. Suppresses the expression of Myb target genes and induces myeloid differentiation and apoptosis.
AdipoGen Naphthol AS-E phosphate
Chemical. CAS 18228-17-6. Formula C17H13ClNO5P. MW 377.72. Synthetic. Histochemical substrate for alkaline phosphatases. Aldolase inhibitor. Small molecule inhibitor. Anticancer compound that directly targets the KIX domain of CBP, resulting in a disrupted CREB-CBP complex, inhibited CREB-target gene induction and inhibited IL-1beta-mediated angiogenic activity in cancer cell lines. Inhibits activity of transcription factor Myb by blocking interaction with KIX domain of coactivator p300 in human leukemia cells. Interferes with the Myb–KIX interaction in vitro and inhibits Myb activity in vivo. Suppresses the expression of Myb target genes and induces myeloid differentiation and apoptosis.