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Filtered Search Results
Medchemexpress LLC Dirithromycin | 62013-04-1 | 98.0% | 1 ML
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Dirithromycin is a potent, orally active, semi-synthetic macrolide antibiotic derived from Erythromycin. It demonstrates activity against gram-positive bacteria, Legionella spp., Helicobacter pylori, and Chlamydia trachomatis. This product is intended for research use only.
- Semi-synthetic macrolide antibiotic
- Derived from Erythromycin
- Active against gram-positive bacteria
- Effective against *Legionella spp.*, *Helicobacter pylori*, and *Chlamydia trachomatis*
- Demonstrates potent *in vitro* activity against *Legionella* and *Helicobacter pylori*
- Effective in experimental infections caused by *S. aureus*, *S. pyogenes*, and *S. pneumoniae*
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Medchemexpress LLC Duocarmycin DM free base | 1116745-06-2 | 463.96 g/mol | C26H26ClN3O3 | 5 MG
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Duocarmycin DM free base is a DNA minor-groove alkylator used as a cytotoxic payload in antibody-drug conjugate (ADC) research and as a reagent for DNA-alkylation studies.
- DNA minor-groove alkylator
- Used as an ADC payload and research reagent for DNA alkylation studies
- CAS number 1116745-06-2
- Molecular formula C26H26ClN3O3
- Molecular weight 463.96 g/mol
- Appearance: light yellow to green yellow solid
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Cambridge Isotope Laboratories CORTISONE (2,3,4-13C3, 98%) CP 97% 100 U, 1 ML
CORTISONE (2,3,4-13C3, 98%) CP 97% 100 U, 1 ML
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Enzo Life Sciences Monensin . sodium salt (1g). CAS: 22373-78-0
Antibiotic that functions as Na+ ionophore. Blocks glycoprotein secretion. Inhibits proliferation of several lymphoma cell lines through cell cycle arrest and apoptosis. Blocks ceramide transport through the Golgi apparatus. Purity: ≥90%. Appearance: White to light yellow powder. Solubility: Soluble in 100% ethanol (25mg/ml), methanol (50mg/ml), chloroform or DMSO (25mg/ml). Slightly soluble in water. Long Term Storage: -20°C.
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Medchemexpress LLC Cd80-in-3 | 486449-65-4 | MFCD32701897 | 98.0% | 323.28 g/mol | C17H10FN3O3 | 100 MG
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CD80-IN-3 is a small-molecule inhibitor that blocks the CD80/CD28 interaction, showing in vitro potency (EC50 = 630 nM) and measurable binding affinity (Kd = 125 nM). It is supplied as a solid and is also available as a DMSO solution for assay use; intended for research use only.
- Potent CD80 inhibitor; inhibits CD80/CD28 interaction (EC50 = 630 nM).
- Measured binding affinity Kd = 125 nM.
- High purity solid suitable for biochemical and cellular assays (98.0%).
- Molecular weight 323.28 g/mol; molecular formula C17H10FN3O3.
- CAS number 486449-65-4 for unambiguous identification.
- Available in milligram quantities and solution formats for assay flexibility.
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Apexbio Technology LLC Cyproheptadine hydrochloride 969-33-5 50mg
Cyproheptadine hydrochloride (969-33-5) is a small-molecule antagonist targeting serotonin (5-HT) and histamine receptors especially the 5-HT2A subtype It is designed to competitively antagonize these receptors thereby regulating serotonergic and histaminergic signaling pathways Cyproheptadine hydrochloride exerts its biological activity primarily through serotonin and histamine receptor antagonism and also exhibits antimuscarinic effects In in vitro studies cyproheptadine hydrochloride demonstrates inhibition of serotonin-enhanced platelet aggregation induced by ADP with an IC50 value commonly reported near 20 nM toward human 5-HT2A receptors Based on these pharmacological properties cyproheptadine hydrochloride holds research potential in antithrombotic studies post-gastrectomy dumping syndrome migraine pruritic dermatoses anorexia and pituitary-dependent Cushing s syndrome
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eMolecules 307519-88-6 | Medchem Express | NMDI14 | 5mg | 446259969 | HY-111374 | MFCD02073967 | 415.51 | C21H25N3O4S
Ambeed | 2-(1H-Imidazol-1-yl)propanoic acid | 250mg | 717401382 | A155633 | 753489-91-7 | MFCD03161186 | 140.142 | C6H8N2O2
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Medchemexpress LLC HY-15067 25mg Medchemexpress, DNQX CAS:2379-57-9 Purity:>98%
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Medchemexpress, HY-15067 25mg DNQX CAS:2379-57-9 DNQX (FG 9041), a quinoxaline derivative, is a selective, potent competitive non-NMDA glutamate receptor antagonist (IC50s = 0.5, 2 and 40 μM for AMPA, kainate and NMDA receptors, 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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eMolecules 81189-92-6 | Medchem Express | Acetyllovastatin | 5mg | 482204294 | HY-126237 | 446.584 | C26H38O6
Medchem Express | Acetyllovastatin | 5mg | 482204294 | HY-126237 | 81189-92-6 | 446.584 | C26H38O6
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eMolecules 1628210-26-3 | Medchem Express | KDM5-IN-1 | 1mg | 446255438 | HY-100422 | MFCD30747843 | 324.388 | C17H20N6O
Medchem Express | Bractoppin | 5mg | 586608695 | HY-126020 | 2290527-07-8 | 414.484 | C25H23FN4O
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Selleck Chemical LLC Darolutamide ODM-201-5mg
Darolutamide (ODM-201, BAY-1841788) is a novel androgen receptor (AR) antagonist that blocks AR nuclear translocation with Ki of 11 nM. Phase 3.
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Selleck Chemical LLC MIK665 S64315-1mg
MIK665 (S64315) is an inhibitor of induced myeloid leukemia cell differentiation protein Mcl-1 with Ki value of 1.2 nM and has potential pro-apoptotic and antineoplastic activities.
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Medchemexpress LLC Dalcetrapib | 211513-37-0 | MFCD06407886 | 99.2% | 389.59 | 50 MG
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Dalcetrapib is an orally active cholesteryl ester transfer protein (CETP) inhibitor. It has shown activity against recombinant human CETP and human plasma CETP, playing a role in cholesterol metabolism research.
- Inhibits cholesteryl ester transfer protein activity
- Increases pre-β-HDL formation
- Increases plasma HDL cholesterol
- Promotes fecal elimination of neutral sterols and bile acids
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CPC Scientific Butyryl-Tyr(Me)-Ile-Gln-Asn-Cys-Pro-Leu-Gly-NH2 (trifluoroacetate salt) 5MG
Carbetocin shows a prolonged effect due to an increased resistance to enzymatic cleavage. Carbetocin is highly effective in preventing post-partum hemorrhage after vaginal delivery.ONE-LETTER SEQUENCE: Butyryl-Y(Me)-INCPLG-NH2MOLECULAR FORMULA: C45H69N11O12S1MOLECULAR WEIGHT:988.18STORAGE CONDITIONS: -20 5C, CAS REGISTRY NUMBER: [37025-55-1], RESEARCH AREA: HormonalREFERENCES: T.Barth et al., Coll. Czech. Chem. Commun., 46, 2441 (1981); N.Cort et al., Am. J. Vet. Res., 43, 1283 (1982); V.Klenerova et al., J. Physiol. Pharmacol., 60, 57 (2009); N.C.Peters and J.J.Duvekot, Obstet. Gynecol. Surv., 64, 129 (2009); W.Rath, Eur. J. Obstet. Gynecol. Reprod. Biol., 147, 15 (2009)
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Medchemexpress LLC Carbetocin acetate | 1631754-28-3 | 99.6% | 1048.21 | 100 MG
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Carbetocin acetate is an oxytocin (OT) analogue and an oxytocin receptor agonist with a Ki of 7.1 nM. It has potential for postpartum hemorrhage research and can cross the blood-brain barrier, producing antidepressant-like activity via activation of oxytocin receptors in the CNS. In vitro, it demonstrates significantly higher stability and a longer duration of action compared to oxytocin.
- Oxytocin analogue and receptor agonist
- High affinity to oxytocin receptor (Ki=7.1 nM)
- Potential for postpartum hemorrhage research
- Crosses blood-brain barrier
- Produces antidepressant-like activity
- Higher stability and longer duration of action in vitro
- Solid, white to off-white appearance
- Chemical formula: C47H73N11O14S
- CAS number: 1631754-28-3
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