Indoles and derivatives
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- (278)
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- (22)
- (7)
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- (3)
- (26)
- (1)
- (176)
- (9)
- (17)
- (39)
- (70)
- (52)
- (9)
- (15)
- (2)
- (2)
- (8)
- (9)
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- (19)
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- (11)
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- (62)
- (16)
- (165)
- (2)
- (1)
- (122)
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- (41)
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- (494)
- (2)
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Filtered Search Results
Aobchem AOBCHEM
5000921907 7-CHLORO-1H-INDAZOLE-4-CARBOXY
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Aobchem AOBCHEM
5000921974 6-BROMO-7-METHYL-1H-INDAZOLE 5
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TARGETMOL CHEMICALS INC --ASARININ 20MG
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Also available in 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. (-)-Asarinin (Eleutheroside B4) shows antibacterial activity. purity: 99%
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Medchemexpress LLC Trans-Ned 19 | 1354235-96-3 | MFCD31562774 | 99.3% | 514.59 g/mol | C30H31FN4O3 | 10 MG
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trans-Ned 19 is a research chemical that functions as a nicotinic acid adenine dinucleotide phosphate (NAADP) antagonist and two-pore channel (TPC) blocker, inhibiting NAADP-mediated calcium (Ca2+) release. It is supplied as a solid for laboratory research use and is characterized by high purity suitable for analytical and biological assays.
- Acts as an NAADP antagonist and TPC blocker.
- Inhibits NAADP-mediated Ca2+ release (reported IC50 ≈ 6 nM).
- High purity appropriate for analytical and biological experiments.
- Supplied as a solid, stable under recommended storage conditions.
- Molecular weight 514.59 g/mol; chemical formula C30H31FN4O3.
- Available in small-milligram quantities for research applications.
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Sigma Aldrich Fine Chemicals Biosciences Yohimbine hydrochloride >=98% (HPLC), powder | 65-19-0 | MFCD00012674 | 1G
Yohimbine hydrochloride >=98% (HPLC), powder | Purity: >=98% (HPLC) | Mol Wt: 390.9 | 65-19-0 | MFCD00012674 | 1G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000743714 GANGLIOSIDE GT1B PO 5MG
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Apexbio Technology LLC Luzindole,5mg CAS# 117946-91-5
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Small and/or specialty supplier based on Federal laws and SBA requirements.
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Luzindole is a melatonin receptor antagonist that preferentially targets MT2 over MT1. Luzindole inhibits experimental autoimmune encephalomyelitis and exerts antidepressant-like activity[1-3]. Luzindole (30 mg/kg i.p.) reduces the immobile time in a dose-dependent manner, reducing midnight by 60% and noon by 39%. Luzindole shows the greatest effect at 60 minutes. In albinism ND/4 mice or C57BL/6J mice that do not produce melatonin, Luzindole (30 mg/kg i.p.) does not change the immobile time at noon or midnight[3]. Other sizes are also available. Please inqury us for quote.
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Enzo Life Sciences PD-146176 (50mg). CAS: 4079-26-9
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A potent and selective 15-lipoxygenase inhibitor which lacks significant nonspecific antioxidant properties. It suppresses atherogenesis and limits atherosclerotic lesion development in the rabbit. It reduces oxidant stress-induced apoptosis in endothelial cells and inhibits proliferation in 15-LO overexpressing PC3 cells. Purity: ≥98% (HPLC). Solubility: Soluble in DMSO (50mg/mL) and ethanol (10mg/mL). Long Term Storage: Ambient.
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Aobchem AOBCHEM
5000937712 2-CHLOROPHENYL 2 3-DIHYDROBE
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Aobchem AOBCHEM
5000969827 3-CHLOROPHENYL -3-THIENYLMETH
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Aobchem AOBCHEM
5000973738 3- 2-FLUOROPHENYL -5-METHYL-1H
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Aobchem AOBCHEM
5001002656 2-CHLORO-5-FLUOROPHENYL PYRR
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Aobchem AOBCHEM
5001015359 2-CHLOROPHENYL 3 5-DICHLOROP
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Aobchem AOBCHEM
5001015445 1- 3-CHLOROPHENYL -4 4-DIFLUOR
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Aobchem AOBCHEM
5001032685 6- 2-CHLOROPHENYL -3-PYRIDINEC
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