Fluorobenzenes
(S)-(-)-1-(4-Fluorophenyl)ethylamine, ChiPros 99%, ee 99%
CAS: 66399-30-2 Molecular Formula: C8H10FN Molecular Weight (g/mol): 139.173 MDL Number: MFCD03092999 InChI Key: QGCLEUGNYRXBMZ-LURJTMIESA-N Synonym: s-1-4-fluorophenyl ethylamine,s-1-4-fluorophenyl ethanamine,1s-1-4-fluorophenyl ethanamine,1s-1-4-fluorophenyl ethylamine,s-1-4-fluoro-phenyl-ethylamine,s---1-4-fluorophenyl ethylamine,1s-1-4-fluorophenyl ethan-1-amine,pubchem15218,5-1-4-fluorophenyl ethanamine,s-4-fluoro-,a-methylbenzylamine PubChem CID: 2779063 IUPAC Name: (1S)-1-(4-fluorophenyl)ethanamine SMILES: CC(C1=CC=C(C=C1)F)N
2,4,6-Trifluoroaniline, 98%
CAS: 363-81-5 Molecular Formula: C6H4F3N MDL Number: MFCD00007650 InChI Key: BJSVKBGQDHUBHZ-UHFFFAOYSA-N Synonym: 2-amino-1,3,5-trifluorobenzene,2,4,6-trifluorobenzenamine,benzenamine, 2,4,6-trifluoro,2,4,6-trifluorophenylamine,pubchem2468,acmc-1cmhu,2,4,6 trifluoroaniline,2,4,6-tri-fluoroaniline,2,4,6-trifluoro aniline,2,4,6-trifluoro-aniline PubChem CID: 67765 IUPAC Name: 2,4,6-trifluoroaniline
Medchemexpress LLC Relamorelin TFA | 2863659-22-5 | 99.8% | 905.00 | 5 MG
Relamorelin TFA, a pentapeptide ghrelin analog, is a selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist with a Ki of 0.42 nM for GHS-1a receptor. It is centrally penetrant, increases growth hormone levels, and accelerates gastric emptying.
- Selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist
- Centrally penetrant
- Increases growth hormone levels
- Accelerates gastric emptying
- Potential for cachexia research
- Potential for gastroparesis research
- Potential for gastric/intestinal dysmobility disorders research
Medchemexpress LLC BAM(8-22) | 412961-36-5 | 99.89% | 1971.20 | 5 MG
BAM(8-22), a proteolytically cleaved product of proenkephalin A and sensory neuron-specific receptor (SNSR) agonist, is a potent activator of Mas-related G-protein-coupled receptors (Mrgprs), specifically MrgprC11 and hMrgprX1. It induces scratching in mice in an Mrgpr-dependent manner. Additionally, BAM(8-22) has an analgesic effect and can inhibit the activation of microglia.
- Potent activator of Mas-related G-protein-coupled receptors (Mrgprs).
- Induces scratching in mice in an Mrgpr-dependent manner.
- Has an analgesic effect.
- Inhibits the activation of microglia.
- Increases miR-184 level in LPS-treated BV-2 cells.
- Reduces Iba-1 and inflammatory cytokines in LPS-treated BV-2 cells.
- Diminishes NMDA-evoked nocifensive behaviors and hyperalgesia in rat pain models.
- Reduces NMDA-evoked expression of FLI and NADPH reactivity in the spinal dorsal horn.
Medchemexpress LLC BAM(8-22) | 412961-36-5 | 99.89% | 1971.20 | 1 MG
BAM(8-22) is a proteolytically cleaved product of proenkephalin A and functions as a sensory neuron-specific receptor (SNSR) agonist. It is a potent activator of Mas-related G-protein-coupled receptors (Mrgprs), including MrgprC11 and hMrgprX1. This compound induces scratching in mice in an Mrgpr-dependent manner and exhibits an analgesic effect.
- Potent activator of Mrgprs
- Induces scratching in mice
- Exhibits an analgesic effect
- Can inhibit the activation of microglia
- Increases miR-184 levels in LPS-treated BV-2 cells
Medchemexpress LLC BAM(8-22) | 412961-36-5 | 99.9% | 1971.20 | 10 MG
BAM(8-22) is a proteolytically cleaved product of proenkephalin A and a sensory neuron-specific receptor (SNSR) agonist. It is a potent activator of Mas-related G-protein-coupled receptors (Mrgprs), specifically MrgprC11 and hMrgprX1. This compound induces scratching in mice in an Mrgpr-dependent manner, exhibits an analgesic effect, and inhibits microglial activation.
- Potent activator of MrgprC11 and hMrgprX1
- Induces scratching in mice in an Mrgpr-dependent manner
- Exhibits an analgesic effect
- Inhibits microglial activation
Medchemexpress LLC Relamorelin TFA | 2863659-22-5 | 99.8% | 905.00 | C45H51F3N8O7S | 10 MG
Relamorelin TFA is the trifluoroacetate salt of Relamorelin (RM-131), a pentapeptide ghrelin/growth hormone secretagogue receptor agonist supplied as a solid for laboratory research. It stimulates growth hormone release and accelerates gastric emptying, and is used in preclinical investigations of gastrointestinal motility and cachexia.
- High purity of 99.8%.
- Molecular weight of 905.00 g/mol.
- CAS number 2863659-22-5.
- Supplied as a solid suitable for bench-top handling and formulation.
- Selective GHSR agonist that increases growth hormone release and accelerates gastric emptying.
- Intended for preclinical research into gastroparesis and cachexia models.
Medchemexpress LLC HY-106067A 10mg Medchemexpress, Dazoxiben CAS:74226-22-5 Purity:>98%
Medchemexpress, HY-106067A 10mg Dazoxiben CAS:74226-22-5 Dazoxiben is a potent and orally active thromboxane (TX) synthase inhibitor. 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.
Medchemexpress LLC Urea, N-(4-chloro-2-hydroxy-3-sulfonylphenyl)-N'-(1R-2-methyl-2-cyclopenten-1-yl) | 1838123-22-0 | 99.4% | 5 MG
(R,R)-CXCR2-IN-2 is the (R,R) diastereomer of CXCR2-IN-2, a selective, brain-penetrant CXCR2 antagonist supplied for preclinical research. It is provided as solid samples and as a 10 mM solution in DMSO.
- Selective CXCR2 antagonist suitable for pharmacology studies.
- Brain-penetrant profile supports CNS-focused experiments.
- High purity and high enantiomeric excess.
- Available as solid samples and as a 10 mM solution in DMSO.
- Molecular weight 414.90 g·mol⁻¹; formula C18H23ClN2O5S.
Medchemexpress LLC HY-10162 2g , Olaparib AZD2281;KU0059436 CAS:763113-22-0 Purity:98%
Medchemexpress, HY-10162 2g Olaparib AZD2281;KU0059436 CAS:763113-22-0 Formula:C24H23FN4O3 IC50: 5/1 nM (PARP-1/2) Purity:98% Olaparib is a potent PARP inhibitor with IC 50 of 5 and 1 nM for PARP-1 and PARP-2 , respectively. 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.
Medchemexpress LLC HY-10162 50mg Medchemexpress, Olaparib CAS:763113-22-0 Purity:>98%
Medchemexpress, HY-10162 50mg Olaparib CAS:763113-22-0 Olaparib (AZD2281; KU0059436) is a potent and orally active PARP inhibitor with IC50s of 5 and 1 nM for PARP1 and PARP2, respectively. Olaparib is an autophagy and mitophagy activator[2][3][4]. 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.