Aminophenols
eMolecules 103-90-2 | Acetaminophen (Standard) | Medchem Express (US) | MFCD00002328 | 151.165 | C8H9NO2 | 98.000 | CC(=O)Nc1ccc(O)cc1 | 25mg | 849677363
Acetaminophen (Standard) | Medchem Express (US) | 103-90-2 | MFCD00002328 | 151.165 | C8H9NO2 | 98.000 | CC(=O)Nc1ccc(O)cc1 | 25mg | 849677363
Medchemexpress LLC RGX-104 hydrochloride | 610318-03-1 | 99.9% | 632.54 | 10 MG
RGX-104 hydrochloride is a small-molecule LXR agonist that modulates innate immunity through the transcriptional activation of the ApoE gene. It is intended for research use only.
- Modulates innate immunity via transcriptional activation of the ApoE gene.
- Potential anti-cancer activity through suppression of various cancer types, including lung cancer, melanoma, glioblastoma, ovarian, renal cell, triple-negative breast, and colon cancer.
- Induces tumor regression in some cases.
- Available in various quantities.
![eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 7mg | 564356416](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000127492.jpg-250.jpg)
eMolecules 86347-15-1 | Medetomidine Hydrochloride | Key Organics/BIONET236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 7mg | 564356416
Medetomidine Hydrochloride | Key Organics/BIONET | 86347-15-1236.740 | C13H17ClN2 | 99.000 | Cl.CC(c1cnc[nH]1)c1cccc(C)c1C | 7mg | 564356416
Medchemexpress LLC LDC4297 (hydrochloride) | 2319747-14-1 | 98.2% | 25 MG
LDC4297 hydrochloride is a selective inhibitor of CDK7, effectively inhibiting human cytomegalovirus (HCMV) replication. It exhibits broad antiviral activities against various virus families including Herpesviridae, Adenoviridae, Poxviridae, Retroviridae, and Orthomyxoviridae. This compound is suitable for infection research.
- Selective inhibitor of CDK7
- Inhibits human cytomegalovirus (HCMV) replication
- Demonstrates broad antiviral activities against multiple virus families
- Useful for infection research
- Solid form storage: 4°C, sealed, away from moisture and light
- In-solvent storage: -80°C for 6 months or -20°C for 1 month, sealed, away from moisture and light
Medchemexpress LLC HY-15373 100mg , Fenretinide 4-HPR;(4-Hydroxyphenyl)retinamide CAS:65646-68-6 Purity:98%
Medchemexpress, HY-15373 100mg Fenretinide 4-HPR;(4-Hydroxyphenyl)retinamide CAS:65646-68-6 Formula:C26H33NO2 Purity:98% Fenretinide is a synthetic retinoid deriverative, binding to the retinoic acid receptors ( RAR ) at concentrations necessary to induce cell death. 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.
eMolecules 487-68-3 | Mesitaldehyde | Ambeed | MFCD00003341 | 148.205 | C10H12O | 95.000 | Cc1cc(C)c(C=O)c(C)c1 | 1000g | 600833343
Mesitaldehyde | Ambeed | 487-68-3 | MFCD00003341 | 148.205 | C10H12O | 95.000 | Cc1cc(C)c(C=O)c(C)c1 | 1000g | 600833343
Medchemexpress LLC Ethylenediaminetetraacetic acid sodium hydrate | 85715-60-2 | MFCD00149675 | 97.0% | 376.20 g/mol | C10H15N2Na3O9 | 25 G
EDTA sodium hydrate (ethylenediaminetetraacetic acid trisodium salt hydrate) is a sodium salt hydrate of EDTA used as a metal chelating agent and laboratory reagent. It binds divalent and trivalent metal ions to stabilize solutions and remove trace metals during buffer preparation, sample cleanup, and analytical assays. Supplied as a crystalline powder for research use.
- High purity (97.0%).
- Effective chelator of Ca2+ and Mg2+.
- Stable crystalline powder, easy to weigh and dissolve.
- Suitable for buffer preparation and analytical assays.
- Available in multiple pack sizes, including 25 g.
- Identified by CAS number 85715-60-2 for traceability.
TARGETMOL CHEMICALS INC MKC-1 5MG
Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 500 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. MKC-1 (Ro-31-7453) is an orally bioavailable small-molecule bisindolylmaleimide cell cycle inhibitor with potential antineoplastic activity. MKC-1 and its metabolites inhibit tubulin polymerization blocking the formation of the mitotic spindle which may result inpurity: 99%
Medchemexpress LLC MRL-494 (hydrochloride) | 2699937-04-5 | 98.6% | 25 MG
MRL-494 hydrochloride is an antibacterial agent that acts as an inhibitor of β-barrel assembly machine A (BamA). It is impervious to efflux and the outer membrane permeability barrier, effectively inhibiting both Gram-positive and Gram-negative bacteria. The agent lethally disrupts the cytoplasmic membrane and inhibits outer membrane protein biogenesis by targeting BamA.
- Impervious to efflux and outer membrane permeability barrier
- Inhibits both Gram-positive and Gram-negative bacteria
- Lethally disrupts cytoplasmic membrane
- Inhibits outer membrane protein biogenesis
Medchemexpress LLC IKK 16 hydrochloride | 1186195-62-9 | 99.95% | 520.09 | 200 MG
IKK 16 hydrochloride | 1186195-62-9 | 99.95% | 520.09 | 200 MG
Medchemexpress LLC NS8593 hydrochloride | 875755-24-1 | 99.76% | 299.80 | 1 MG
NS8593 hydrochloride is a potent and selective inhibitor of small conductance Ca2+-activated K+ channels (SK channels). It reversibly inhibits SK3-mediated currents with a Kd value of 77 nM. NS8593 hydrochloride inhibits all SK1-3 subtypes in a Ca2+-dependent manner (Kds of 0.42, 0.60, and 0.73 μM, respectively, at 0.5 μM Ca2+), but does not affect intermediate and large conductance Ca2+-activated K+ channels (hIK and hBK channels, respectively). It is for research use only and not sold to patients.
- Potent and selective small conductance Ca2+-activated K+ channels inhibitor
- Reversibly inhibits SK3-mediated currents with a Kd value of 77 nM
- Inhibits SK1-3 subtypes Ca2+-dependently
- Does not affect intermediate and large conductance Ca2+-activated K+ channels
- Affects firing rate and firing pattern of dopaminergic neurons in vivo in C57Bl/6 mice at doses of 3 and 10 mg/kg intravenously
Medchemexpress LLC Riluzole hydrochloride | 850608-87-6 | 99.9% | 500 MG
Riluzole hydrochloride is an anticonvulsant agent that functions as a use-dependent Na+ channel blocker and can also inhibit GABA uptake with an IC50 of 43 μM. It is intended for research use only and not sold to patients.
- Acts as an anticonvulsant agent.
- Inhibits Na+ channels.
- Can inhibit GABA uptake.