Bioactive Small Molecules
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Filtered Search Results
Medchemexpress LLC Ephrin B3 Rat HEK2 10ug
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Ephrin B3 Protein a member of the ephrin family lacks conserved residue(s) crucial for feature annotation propagation This unique molecular profile suggests distinct functional properties and interactions within the ephrin family Investigating the specific role and implications of this divergence in conserved residues is crucial to understand Ephrin B3 s functional nuances and cellular significance in biological processes Ephrin B3 Protein Rat (HEK293 His) is the recombinant rat-derived Ephrin B3 protein expressed by HEK293 with C-His labeled tag
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Medchemexpress LLC HY-130853 250mg Medchemexpress, Thalidomide-NH-PEG2-C2-NH-Boc CAS:2097509-40-3 Purity:>98%
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Medchemexpress, HY-130853 250mg Thalidomide-NH-PEG2-C2-NH-Boc CAS:2097509-40-3 Thalidomide-NH-PEG2-C2-NH-Boc is a synthesized E3 ligase ligand-linker conjugate that incorporates the Thalidomide based cereblon ligand and a PEG linker used for dBRD9 (compound 6) synthesis. dBRD9 is a selective BRD9 probe PROTAC degrader for the study of BAF complex biology. 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 4-Methylthio-N-benzylcathinone (hydrochloride), Purity: ≥98%, CAS: 2706488-88-0, 5 mg
An analytical reference standard categorized as a cathinone; intended for research and forensic applications
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Cayman Chemical 4-Fluoroethcathinone (hydrochloride), Purity: ≥98%, CAS: 2705473-25-0, 5 mg
A structural analog of 4-FMC, with an ethyl group replacing the amino terminal methyl group; intended to be used for research and forensic applications
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![Cayman Chemical N6-[(6-Aminohexyl)carbamoylmethyl]-ADP, Purity: ≥70%, CAS: 100826-95-7, 5 mg](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502918723.png-250.jpg)
Cayman Chemical N6-[(6-Aminohexyl)carbamoylmethyl]-ADP, Purity: ≥70%, CAS: 100826-95-7, 5 mg
An alkylated ADP derivative; has been biotinylated and conjugated to an azidonitrobenzoyl group for use as a photoaffinity probe to visualize the ATPase site of rabbit myosin
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Medchemexpress LLC Octan-2-yl 2-cyanoac 50mg | 133978-15-1 | 209.28 g·mol⁻¹ | C12H19NO2 | 50 MG
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Octan-2-yl 2-cyanoacrylate is a cyanoacrylate ester used as a fast-curing adhesive and tissue adhesive in research applications. Supplied for research use only, it polymerizes to form a flexible, durable film and is commonly used in adhesive testing, biomaterials research, and surgical adhesive studies.
- Fast-curing cyanoacrylate adhesive for rapid bonding.
- Forms a flexible, durable polymer film after curing.
- Suitable for tissue adhesive research applications.
- Available in small research quantities, improving handling for lab studies.
- Characterized by datasheet, COA, and SDS for research validation.
- Not for use in patients; intended for research use only.
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Medchemexpress LLC PI3K/mTOR Inhibitor-11 | 2845104-25-6 | C27H21N7 | 5 MG
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PI3K/mTOR Inhibitor-11 | 2845104-25-6 | C27H21N7 | 5 MG
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Cayman Chemical R18 (trifluoroacetate salt), Purity: ≥95%, 5 mg
A peptide inhibitor of the 14-3-3-Raf-1 protein-protein interaction; binds to 14-3-3τ, -β, and -ζ (Kds = 7.1, 7, and 8.9 nM, respectively) and inhibits 14-3-3τ binding to Raf-1 in a filter binding assay at 5 nM; inhibits 14-3-3ζ-mediated protection of Raf-1 from phosphatase-induced inactivation
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Selleck Chemical LLC Cefuroxime E4838-5MG
Cefuroxime (Kefurox) is an orally active second-generation broad-spectrum cephalosporin antibiotic with increased stability to -lactamase Cefuroxime exhibits broad-spectrum activity against Gram-positive bacteria including penicillinase-producing staphylococci and non- -lactamase-producing gram-negative bacteria
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Cayman Chemical Celgosivir, Purity: ≥98%, CAS: 121104-96-9, 5 mg
An α-glucosidase inhibitor (IC50 = 0.7 µg/ml) and a prodrug form of castanospermine; reduces BVDV levels in a plaque formation assay (IC50 = 16 mM) and increases survival of MDBK infected with BVDV (IC50 = 47 µM); reduces viremia and increases survival of mice infected with a lethal dose of dengue virus at 50 mg/kg twice daily, i.p.
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Cayman Chemical t-TUCB, Purity: ≥98%, CAS: 948304-40-3, 25 mg
An sEH inhibitor (IC50s = 0.4, 3.1, and 11.9 nM for the human, mouse, and rat enzymes, respectively); inhibits FAAH (IC50 = 260 nM for the human enzyme); increases the mechanical paw withdrawal threshold in a streptozotocin-induced mouse model of diabetic neuropathic pain at 3 mg/kg; prevents isoproterenol-induced EKG abnormalities, as well as reduces isoproterenol-induced increases in infarct size and heart weight, in a rat model of myocardial ischemia at 3, 10, and 30 mg/kg
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Medchemexpress LLC Fipexide hydrochloride | 34161-23-4 | 99.88% | 1 ML
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Fipexide hydrochloride is a parachloro-phenossiacetic acid derivative and an orally active nootropic agent. It reduces striatal adenylate cyclase activity and has a positive effect on cognitive performance through dopaminergic neurotransmission. It is used for senile dementia research and acts as a chemical inducer in callus formation, shoot regeneration, and Agrobacterium infection.
- Parachloro-phenossiacetic acid derivative.
- Orally active nootropic agent.
- Reduces striatal adenylate cyclase activity.
- Positive effect on cognitive performance.
- Used for senile dementia research.
- Chemical inducer in callus formation, shoot regeneration, and Agrobacterium infection.
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Medchemexpress LLC Flaviviruses-IN-3 | 420090-97-7 | C26H23N3O4S | 5 MG
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Flaviviruses-IN-3 is a potent flavivirus inhibitor. It reduces West Nile virus (WNV) protease activity, showing an inhibition of 54%. This compound is intended for research use only.
- Potent flavivirus inhibitor.
- Reduces West Nile virus protease activity.
- High purity: 98.93%.
- Available in various quantities for research needs.
- Provided with detailed documentation including data sheet, COA, SDS, and handling instructions.
- Enables targeted research on flaviviruses.
- Offers a tool for studying WNV protease activity.
- Ensures reliable experimental results due to high purity.
- Supports various experimental setups with different solubility protocols for in vitro and in vivo studies.
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Medchemexpress LLC PACAP (1-27) | 127317-03-7 | 99.3% | 3147.66 | 5 MG
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PACAP (1-27), human, ovine, rat (PACAP 1-27) is the N-terminal fragment of PACAP-38. It is a potent PACAP receptor agonist with IC50s of 3 nM for rat PAC1, 2 nM for rat VPAC1, and 5 nM for human VPAC2. This product is for research use only.
- Potent PACAP receptor agonist
- N-terminal fragment of PACAP-38
- Displaces radioligand binding in PAC-receptors on AR4-2J cells
- Stimulates IP3 and cAMP formation in AR4-2J cells
- Reduces total pulmonary resistance in guinea-pigs
- Inhibitory effect on pulmonary resistance similar to salbutamol
- Increases heart rate less than salbutamol
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Cayman Chemical BAY-293, Purity: ≥98%, CAS: 2244904-70-7, 25 mg
An inhibitor of the K-Ras-SOS1 protein-protein interaction (IC50 = 0.021 µM); inhibits proliferation of K562 and MOLM-13 cells expressing wild-type K-RAS as well as NCI H358 and Calu-1 cells expressing mutant K-RASG12C (IC50s = 1.09, 0.995, 3.48, and 3.19 µM, respectively)
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