Organozinc
Cayman Chemical MRS2179 ammonium salt hydrat
A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective for P2Y1 over P2Y2, P2Y4, P2Y6, P2Y12, and P2Y13, as well as P2X1-4, receptors at 10 µM; reduces 2-MeSADP-induced PLC activity (IC50 = 331 nM in turkey erythrocyte membranes); inhibits ADP-induced platelet shape change and aggregation in washed isolated human platelets at 10 µM; prolongs the length of tail bleeding time in mice, as well as decreases platelet thrombus formation in a mouse model of iron chloride-induced arterial thrombosis at 50 mg/kg
![eMolecules 3-Ethoxy-3-oxopropylzinc bromide | Rieke Metals | 193065-68-8 | MFCD00671976 | 246.410 | C5H9BrO2Zn | 0.000 | [Br-].CCOC(=O)CC[Zn+] | 100ml | 118909162](https://assets.fishersci.com/TFS-Assets/CCG/product-images/NC1662172.jpg-250.jpg)
eMolecules 3-Ethoxy-3-oxopropylzinc bromide | Rieke Metals | 193065-68-8 | MFCD00671976 | 246.410 | C5H9BrO2Zn | 0.000 | [Br-].CCOC(=O)CC[Zn+] | 100ml | 118909162
3-Ethoxy-3-oxopropylzinc bromide | Rieke Metals | 193065-68-8 | MFCD00671976 | 246.410 | C5H9BrO2Zn | 0.000 | [Br-].CCOC(=O)CC[Zn+] | 100ml | 118909162
Medchemexpress LLC Oxypeucedanin hydrate | 2643-85-8 | 10 MM 1 ML
Oxypeucedanin hydrate is a natural product isolated from *D. anethifolia* and classified as a phenylpropanoid and coumarin. This laboratory chemical is used in the manufacture of substances and exhibits mild toxicity on fibroblasts and parental lymphoma cells.
- Natural product
- Isolated from *D. anethifolia*
- Classified as a phenylpropanoid and coumarin
- Exhibits mild toxicity on fibroblasts and parental lymphoma cells
- Molecular weight: 304.29
- Formula: C16H16O6
- Appearance: Solid
- Color: Off-white to light yellow
- Storage as powder: -20°C for 3 years, 4°C for 2 years
- Storage in solvent: -80°C for 6 months, -20°C for 1 month
Cayman Chemical MRS2179 ammonium salt hydrat
A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective for P2Y1 over P2Y2, P2Y4, P2Y6, P2Y12, and P2Y13, as well as P2X1-4, receptors at 10 µM; reduces 2-MeSADP-induced PLC activity (IC50 = 331 nM in turkey erythrocyte membranes); inhibits ADP-induced platelet shape change and aggregation in washed isolated human platelets at 10 µM; prolongs the length of tail bleeding time in mice, as well as decreases platelet thrombus formation in a mouse model of iron chloride-induced arterial thrombosis at 50 mg/kg
Medchemexpress LLC Claudin 18.2 antibody | 10 UL
This rabbit-derived, non-conjugated IgG polyclonal antibody targets Claudin 18.2 for research use. It is affinity purified and supplied in 1*PBS (pH 7.4), 0.2% BSA, 50% Glycerol, with 0.05% Sodium Azide as a preservative. It should be stored at -20°C for 1 year, avoiding repeated freeze/thaw cycles.
- Targets Claudin 18.2
- For research use only
- Affinity purified
- Supplied in PBS, BSA, and Glycerol
- Contains Sodium Azide as a preservative
- Observe 35 kDa molecular weight
- Stable for 1 year when stored at -20°C
- Avoid repeated freeze/thaw cycles
Strem, An Ascensus Company CAS# 14074-80-7. 250mg. Zinc meso-tetraphenylporphine. MFCD00012155
CAS# 14074-80-7. 250mg. Zinc meso-tetraphenylporphine. MFCD00012155. Molecular Weight: 678.10. Molecular Formula: (C44H28N4)Zn. Color/form: purple xtl. Strem# 30-3500. http://www.strem.com/catalog/v/30-3500/
Med Vet International Potassium Gluconate Tablets
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Potassium gluconate Tablet supplement that is used for Hypokalemia or low blood potassium levels in cats and dogs.
Frontier Specialty Chemicals 250mg Zn(II) meso-Tetraphenylporphine (1-3% chlorin), 14074-80-7 MFCD00012155
This item has a minimum qty of 4 per supplier requirements.
Zn(II) meso-Tetraphenylporphine (1-3% chlorin) CAS: 14074-80-7 MFCD00012155 Porphyrins Synthetic Porphyrins
eMolecules Nilotinib hydrochloride monohydrate | Combi-Blocks | 923288-90-8 | MFCD18251359 | 584.000 | C28H25ClF3N7O2 | 98.000 | O.Cl.Cc1cn(cn1)-c1cc(NC(=O)c2ccc(C)c(Nc3nccc(n3)-c3cccnc3)c2)cc(c1)C(F)(F)F | 5g | 342889881
Nilotinib hydrochloride monohydrate | Combi-Blocks | 923288-90-8 | MFCD18251359 | 584.000 | C28H25ClF3N7O2 | 98.000 | O.Cl.Cc1cn(cn1)-c1cc(NC(=O)c2ccc(C)c(Nc3nccc(n3)-c3cccnc3)c2)cc(c1)C(F)(F)F | 5g | 342889881
![eMolecules 2-Methylphenylzinc iodide | Rieke Metals | 312693-23-5 | MFCD01311452 | 283.420 | C7H7IZn | 0.000 | [I-].Cc1ccccc1[Zn+] | 50ml | 118909617](https://assets.fishersci.com/TFS-Assets/CCG/product-images/NC1675451.jpg-250.jpg)
eMolecules 2-Methylphenylzinc iodide | Rieke Metals | 312693-23-5 | MFCD01311452 | 283.420 | C7H7IZn | 0.000 | [I-].Cc1ccccc1[Zn+] | 50ml | 118909617
2-Methylphenylzinc iodide | Rieke Metals | 312693-23-5 | MFCD01311452 | 283.420 | C7H7IZn | 0.000 | [I-].Cc1ccccc1[Zn+] | 50ml | 118909617
Cayman Chemical MRS2179 ammonium salt hydrat
A competitive purinergic P2Y1 receptor antagonist (Kb = 102 nM); selective for P2Y1 over P2Y2, P2Y4, P2Y6, P2Y12, and P2Y13, as well as P2X1-4, receptors at 10 µM; reduces 2-MeSADP-induced PLC activity (IC50 = 331 nM in turkey erythrocyte membranes); inhibits ADP-induced platelet shape change and aggregation in washed isolated human platelets at 10 µM; prolongs the length of tail bleeding time in mice, as well as decreases platelet thrombus formation in a mouse model of iron chloride-induced arterial thrombosis at 50 mg/kg
Sigma Aldrich Fine Chemicals Biosciences 2-Methoxyethanol suitable1L
2METHOXYETHANOL82 2-Methoxyethanol suitable1L