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Filtered Search Results
eMolecules Medchem Express / CYM-5541 / 5mg / 446256794 / HY-101419 / / 945128-26-7 / MFCD09782785 / 316.445 / C19H28N2O2
Medchem Express / CYM-5541 / 5mg / 446256794 / HY-101419 / / 945128-26-7 / MFCD09782785 / 316.445 / C19H28N2O2
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American Radiolabeled Chemicals Inc QUININE-ME-3H 250UC
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Quinine-methyl-3H 250uCi in ethanol, 1 mCi/ml, 60-90 Ci/mmol, M.W. 324.4, Shipped in Dry Ice, Exclusive
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Medchemexpress LLC HY-100521 10mg Medchemexpress, GKI-1 CAS: Purity:>98%
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Medchemexpress, HY-100521 10mg GKI-1 CAS: GKI-1 is a Greatwall (GWL) kinase inhibitor with IC50s of 4.9 and 2.5 µM against hGWLFL and hGWL-KinDom, respectively. GKI-1 robustly inhibits ROCK1 with an IC50 of 11 µM, but only weakly affected PKA. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-100224 10mg Medchemexpress, SANT-1 CAS:304909-07-7 Purity:>98%
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Medchemexpress, HY-100224 10mg SANT-1 CAS:304909-07-7 SANT-1 is a potent Smo antagonist, inhibits Hedgehog signaling, with IC50s of 20 nM and 30 nM in Shh-LIGHT2 and SmoA1-LIGHT2 assay, respectively. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Medchemexpress LLC HY-100229 10mg Medchemexpress, Aloxistatin CAS:88321-09-9 Purity:>98%
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Medchemexpress, HY-100229 10mg Aloxistatin CAS:88321-09-9 Aloxistatin (E64d) is a cell-permeable and irreversible broad-spectrum cysteine protease inhibitor. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Cayman Chemical ThIamphenIcol 5g
An antibiotic derived from chloramphenicol that displays a similar spectrum of activity with enhanced potency
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Medchemexpress LLC IL-17 modulator 4 | 2446803-65-0 | 99.0% | C27H34N6O2 | 10MG
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IL-17 modulator 4 is a small-molecule research compound that modulates interleukin-17 (IL-17) signaling. Supplied as a solid reagent at high purity, it is intended for preclinical biochemical and cellular studies to support investigations into IL-17-related pathways and inflammation.
- High purity (99.0%) suitable for biochemical and cellular assays.
- Solid form for convenient storage and handling.
- Relevant for IL-17 pathway and inflammation research.
- Available in multiple milligram scales for dose-ranging studies.
- Molecular formula C27H34N6O2 and molecular weight 474.60 g/mol.
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eMolecules EMOLECULES INC
5000474210 AZITHROMYCIN 500G
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eMolecules Synthonix - Stock / (5-Nitropyridin-2-yl)methanol / 100mg / 525922096 / N42784 / / 36625-57-7 / MFCD07368186 / 154.125 / C6H6N2O3
Synthonix - Stock / (5-Nitropyridin-2-yl)methanol / 100mg / 525922096 / N42784 / / 36625-57-7 / MFCD07368186 / 154.125 / C6H6N2O3
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![eMolecules Medchem Express / PF-06380101-d8 / 5mg / 686240310 / HY-12522S / / / [null] / 751.070 / C39H62N6O6S](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502480098.JPG-250.jpg)
eMolecules Medchem Express / PF-06380101-d8 / 5mg / 686240310 / HY-12522S / / / [null] / 751.070 / C39H62N6O6S
Medchem Express / PF-06380101-d8 / 5mg / 686240310 / HY-12522S / / / [null] / 751.070 / C39H62N6O6S
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Sigma Aldrich Fine Chemicals Biosciences (Z)-Guggulsterone >=89% (HPLC), powder | 39025-23-5 | MFCD01310757 | 5MG
(Z)-Guggulsterone >=89% (HPLC), powder | Purity: >=89% (HPLC) | Mol Wt: 312.45 | 39025-23-5 | MFCD01310757 | 5MG
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AdipoGen Rapamycin (5 mg)
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Rapamycin (5 mg), Adipogen Life Sciences. Chemical. CAS: 53123-88-9. Formula: C51H79NO13. MW: 914.2. Isolated from Streptomyces hygroscopicus. Antibiotic. Antibacterial and antifungal properties. Forms a complex with FKBP12 and inhibits the mammalian target of rapamycin (mTOR). Inhibits the response to interleukin-2 (IL-2), and thereby blocks activation of T and B cells. Potent immunosuppressant used as an alternative to calcineurin inhibitors. Restricts the proliferation of smooth-muscle cells by blocking cell cycle progression at the G1/S transition. Anti-proliferative. Antitumor compound. Apoptosis enhancer. Activator of autophagy both in vitro and in vivo. Anti-HIV and anti-aging compound. Neuroprotective. Suppressor for self-renewal and vascular differentiation potential in hemangioma stem cells.
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American Radiolabeled Chemicals Inc LINOLEOYL ETH 1-3H 250UC
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Linoleoyl ethanolamide-1-3H 250uCi in ethanol, 1 mCi/ml, S.A. 40-60 Ci/mmol, M.W. 323.0, Shipped in Dry Ice, Exclusive
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American Radiolabeled Chemicals Inc RTI-22-125I 25UC
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RTI-55-125I 25uCi in ethanol:water:acetonitrile (1:1:0.1), 1 mCi/ml, S.A. 2200 Ci/mmol, M.W. 385.2
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Medchemexpress LLC 5-(3-amino-1H-indazol-6-yl)-1-[(3-chlorophenyl)methyl]pyridin-2-one | 2095704-43-9 | MFCD31728203 | 98.5% | 350.80 | C19H15ClN4O | 5 MG
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SLV-2436 is a small-molecule, ATP-competitive inhibitor of MAP kinase-interacting kinases MNK1 and MNK2 intended for research use to probe MNK-dependent signaling. It exhibits low-nanomolar potency and is supplied as a solid or as a DMSO solution.
- Inhibits MNK1 (IC50 10.8 nM) and MNK2 (IC50 5.4 nM).
- High purity (≈98.5% by HPLC).
- Molecular formula C19H15ClN4O; molecular weight 350.80 g·mol⁻¹.
- Available as a solid and as a 10 mM DMSO solution for easy dosing.
- Available in small research pack sizes suitable for assay work.
- Recommended storage: powder -20°C; in solvent -80°C for long-term storage.
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