Bioactive Small Molecules
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Filtered Search Results
Medchemexpress LLC Benzonitrile, 3-fluoro-5-[3-(5-fluoro-2-pyridinyl)-1,2,4-oxadiazol-5-yl]- | 327056-26-8 | 99.9% | 284.22 | 50 MG
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Benzonitrile, 3-fluoro-5-[3-(5-fluoro-2-pyridinyl)-1,2,4-oxadiazol-5-yl]- | 327056-26-8 | 99.9% | 284.22 | 50 MG
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Medchemexpress LLC Fazamorexant | 1808918-69-5 | C25H25FN4O2 | 100 MG
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Fazamorexant is an orally active dual orexin receptor antagonist with an IC50 of 32 nM against OX1R and 41 nM against OX2R. It prolongs total sleep time and improves sleep efficiency, making it suitable for research on insomnia.
- Orally active dual orexin receptor antagonist
- Potently inhibits OX1R (IC50 = 32 nM) and OX2R (IC50 = 41 nM)
- Prolongs total sleep time
- Improves sleep efficiency
- Applicable for research on insomnia
- Selectively blocks OX1R and OX2R in vivo
- Promotes rapid onset of sleep by inhibiting wake-promoting neurons
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Cayman Chemical 1-Palmitoyl-3-Linolenoyl-rac-glycerol, Purity: ≥98%, CAS: 126281-90-1, 5 mg
A diacylglycerol containing palmitic acid and α-linolenic acid at the sn-1 and sn-3 positions, respectively; has been found in the peel and pulp of unripe Dwarf Cavendish bananas
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Medchemexpress LLC HY-113004 50mg Medchemexpress, 3-Hydroxyvaleric acid CAS:10237-77-1 Purity:>98%
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Medchemexpress, HY-113004 50mg 3-Hydroxyvaleric acid CAS:10237-77-1 3-Hydroxyvaleric acid is a 5-carbon ketone body. 3-Hydroxyvaleric acid is anaplerotic, meaning it can refill the pool of TCA cycle intermediates. 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 LXR-623, Purity: ≥98%, CAS: 875787-07-8, 1 mg
An LXR modulator that acts as a partial agonist at LXRα and a full agonist at LXRβ (IC50s = 179 and 24 nM, respectively); orally bioavailable and readily passes the BBB; anti-atherogenic in animal models of atherosclerosis
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Cayman Chemical IAXO-102, Purity: ≥95%, CAS: 1115270-63-7, 5 mg
A glycolipid TLR4 antagonist; inhibits lipid A-induced TLR4 activation in a cell-based assay (IC50 = 5.013 µM); reduces LPS-induced lethality in mice at 10 mg/kg; decreases angiotensin II-induced aortic expansion and rupture, as well as the incidence of abdominal aortic aneurysms, in ApoE-/- mice at 3 mg/kg
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Cayman Chemical DNP-INT, Purity: ≥98%, CAS: 69311-70-2, 10 mg
An electron transport inhibitor in plants; competitively inhibits plastoquinol oxidation by binding at the Qo site of cytochrome b6f (Kd = 1.4 nM); inhibits electron flow from water to NADP or methylviologen by 50 and 100% when used at concentrations of 0.5 or 5 µM, respectively
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Cayman Chemical Ac-WEAD-pNA (trifluoroacetate salt), Purity: ≥95%, 5 mg
A colorimetric caspase-1 and caspase-4 substrate; cleavage of the WEAD peptide sequence releases pNA, which can be quantified by colorimetric detection at 405 nm as a measure of caspase-1 and caspase-4 activity
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Cayman Chemical Z944, Purity: ≥98%, CAS: 1199236-64-0, 5 mg
A T-type calcium channel inhibitor (IC50s = 0.050-0.160 µM for human recombinant Cav3.1, Cav3.2, and Cav3.3); selective for T-type channels over the Cav2.2 channel (IC50 = 11 µM), as well as rat Cav1.2, hERG/Kv11.1, and human Nav1.5 channels (IC50s = 32, 7.8, and 100 µM, respectively); reduces seizure duration and the amount of time spent in seizures in a rat model of absence epilepsy at 30 mg/kg
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Cayman Chemical Ribitol, Purity: ≥98%, CAS: 488-81-3, 25 g
A pentose sugar alcohol; a component of the glycopolymer teichoic acid in bacterial cell walls; levels are increased in the brain, cerebrospinal fluid, urine, and plasma of a patient with RPI deficiency
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Medchemexpress LLC 1,10-bis(pyridinium)decane | 6266-40-6 | MFCD00031922 | 99.7% | 458.27 g/mol | C20H30Br2N2 | 5 MG
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1,10-Bis(pyridinium)decane is a biscationic pyridinium salt used as a biochemical research reagent. It acts as an acetylcholinesterase (AChE) inhibitor with a reported IC50 of 25.8 nM and is supplied at high purity for in vitro pharmacology and enzymology studies. Available in milligram-scale quantities for laboratory use.
- Bicationic pyridinium salt suitable for cholinesterase research
- Reported AChE IC50 of 25.8 nM
- High purity: 99.66%
- Molecular weight: 458.27 g/mol
- Chemical formula: C20H30Br2N2
- Supplied in milligram-scale pack sizes for laboratory experiments
- For research use only
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Medchemexpress LLC HY-B1272 100mg , Desipramine (hydrochloride) CAS:58-28-6 Purity:>98%
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HY-B1272 100mg Desipramine (hydrochloride) CAS: 58-28-6 Desipramine hydrochloride is an inhibitor of norepinephrine transporter (NET), 5-HT transporter (SERT) and dopamine transporter (DAT) with Kis of 4, 61 and 78,720 nM, 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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Cayman Chemical KX2-391, Purity: ≥98%, CAS: 897016-82-9, 100 mg
A Src kinase inhibitor (IC50 = ~20 nM); selective for Src over PDGFR, EGFR, JAK1, JAK2, Lck, and ZAP-70; induces cell cycle arrest at the G2/M phase and apoptosis in ERα-positive breast cancer cells; inhibits the growth of Huh7, PLC/PRF/5, Hep3B, and HepG2 cells (GI50s = 9, 13, 26, and 60 nM, respectively); decreases spleen weight and the number of splenic leukemia cells in a mouse model of FLT3-ITD-F691L AML
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Medchemexpress LLC Alpha-Gliadin (43-49) (Gliadorphin) | 107936-65-2 | MFCD00080188 | 99.8% | 875.97 | 50 MG
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Alpha-Gliadin (43-49), also known as Gliadorphin, is a peptide that serves as the major protein component of gluten. This product can be utilized in studies involving the immunological response to alpha-gliadin.
- Primary protein component of gluten
- Inhibits the production of lymphokine activities by mononuclear leukocytes
- Can be used in immunological response research to alpha-gliadin
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Apexbio Technology LLC Lomeguatrib 192441-08-0 50mg
Lomeguatrib (CAS 192441-08-0) is a potent inhibitor of O6-alkylguanine-DNA methyltransferase (MGMT) an enzyme involved in DNA repair that mitigates the cytotoxic effects of alkylating agents In MCF-7 cells Lomeguatrib inactivates MGMT with an approximate IC50 of 6 nM By suppressing MGMT activity Lomeguatrib sensitizes MGMT-expressing cell lines such as A375P and select mutBRAF and mutNRAS melanoma models to temozolomide but does not alter sensitivity to dacarbazine Clinical investigations have demonstrated dose-dependent inactivation of MGMT in patient-derived tumor tissues and peripheral blood mononuclear cells highlighting Lomeguatrib s value as a research tool for studying MGMT-mediated resistance mechanisms in cancer
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