Pyrroles
Apexbio Technology LLC Almotriptan Malate 181183-52-8 100mg
Almotriptan Malate (CAS 181183-52-8) is a small molecule belonging to the triptan class acting as a selective agonist at 5-hydroxytryptamine 1B/1D (5-HT1B/1D) receptors By stimulating these receptors Almotriptan modulates cranial vasoconstriction and inhibits the release of pro-inflammatory neuropeptides biologically counteracting migraine pathophysiology In research applications Almotriptan Malate is utilized to investigate serotonergic signaling pathways migraine mechanisms and the pharmacodynamics of 5-HT1B/1D receptor modulation in neurological models
Accela Chembio Inc Pyrrole-3-carboxylic Acid | 1g | 931-03-3 | MFCD00800594 | 97+% | Shelf Life: 1260 Days | Light Sensitive
Pyrrole-3-carboxylic Acid | 1g | 931-03-3 | MFCD00800594 | 97+% | Shelf Life: 1260 Days | Light Sensitive
eMolecules Medchem Express / Olverembatinib (dimesylate) / 5mg / 533802555 / HY-15666A / / 1421783-64-3 / MFCD26142656 / 724.770 / C31H35F3N6O7S2
Medchem Express / Olverembatinib (dimesylate) / 5mg / 533802555 / HY-15666A / / 1421783-64-3 / MFCD26142656 / 724.770 / C31H35F3N6O7S2
Chem-Impex International, Inc. Indole-3-Carboxylic acid | 771-50-6 | MFCD00005624 | 5G
Indole-3-Carboxylic acid, 771-50-6, MFCD00005624, 5G
Medchemexpress LLC JNJ-63576253 | 25MG
JNJ-63576253 (TRC-253) is a potent and orally active full antagonist of androgen receptor (AR) with IC50s of 37 and 54 nM for F877L mutant AR and wild-type AR in LNCaP cells JNJ-63576253 can be used for the research of castration-resistant prostate cancer (CRPC)[1]
Medchemexpress LLC TLR7 agonist 3 | 1229024-78-5 | 99.9% | 312.41 g/mol | C18H24N4O | 100 MG
TLR7 agonist 3 is a small-molecule agonist of Toll-like receptor 7 used as a research reagent to stimulate innate immune responses and evaluate anticancer immunomodulatory strategies. It is supplied as a high-purity solid suitable for in vitro and in vivo studies.
- Potent agonist of Toll-like receptor 7 (TLR7) for immune activation studies.
- Applicable for conjugation to targeting ligands to direct activity to specific cell types.
- High purity solid suitable for analytical and biological assays.
- Soluble in DMSO (100 mg/mL) and ethanol (≥50 mg/mL); compatible with common in vivo formulations at ≥2.5 mg/mL.
- Offered in multiple pack sizes including 100 mg for dosing flexibility.
![eMolecules ChemScene / 2-(2-((4-Bromo-2-fluorophenoxy)methyl)phenyl)-4455-tetramethyl-132-dioxaborolane / 100mg / 717420696 / CS-0518200 / 0.000 / 2246573-09-9 / [null] / 407.090 / C19H21BBrFO3](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502454873.PNG-250.jpg)
eMolecules ChemScene / 2-(2-((4-Bromo-2-fluorophenoxy)methyl)phenyl)-4455-tetramethyl-132-dioxaborolane / 100mg / 717420696 / CS-0518200 / 0.000 / 2246573-09-9 / [null] / 407.090 / C19H21BBrFO3
ChemScene / 2-(2-((4-Bromo-2-fluorophenoxy)methyl)phenyl)-4455-tetramethyl-132-dioxaborolane / 100mg / 717420696 / CS-0518200 / 0.000 / 2246573-09-9 / [null] / 407.090 / C19H21BBrFO3
Medchemexpress LLC HY-12810 10mg Medchemexpress, EHop-016 CAS:1380432-32-5 Purity:>98%
Medchemexpress, HY-12810 10mg EHop-016 CAS:1380432-32-5 EHop-016 is a potent and selective Rac GTPase Rac1 and Rac3 inhibitor. EHop-016 inhibits Rac1 activity with an IC50 of 1.1 μM in MDA-MB-435 cells. EHop-016 inhibits Vav2 interaction with Rac, Rac-activated PAK1, lamellipodia formation, and cell migration. 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.
eMolecules 1-(4-Iodophenyl)pyrrole | 92636-36-7 | 5G | Purity: 95%
Combi-Blocks | 1-(4-Iodophenyl)pyrrole | 5G | 92636-36-7 | MFCD00052399
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eMolecules 2-AMINO-4-CHLORO-5-FLUOROPYRIMIDINE | 1683-75-6 | MFCD09746440 | 1g
AstaTech | 2-AMINO-4-CHLORO-5-FLUOROPYRIMIDINE | 1g | 402180297 | 26356 | 95.000 | 1683-75-6 | MFCD09746440 | 147.540 | C4H3ClFN3
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Medchemexpress LLC AZ PFKFB3 26 | 1704740-52-2 | MFCD30742931 | 99.2% | 402.49 g·mol-1 | C24H26N4O2 | 50 MG
AZ PFKFB3 26 is a research-grade small-molecule inhibitor of PFKFB3 (CAS 1704740-52-2) supplied as a powder for in vitro and preclinical studies. The compound has formula C24H26N4O2 and a molecular weight of 402.49 g·mol-1. Analytical data and handling information are provided to support experimental use.
- Documented purity available (COA shows ~99.2%).
- Suitable for in vitro studies; soluble in DMSO at ~5 mg/mL.
- Analytical data provided: COA, H NMR, LCMS, and SDS.
- Storage conditions specified for powder and solutions to preserve stability.
- Available in multiple research sizes, including 50 mg.