Indoles and derivatives
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- (1)
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- (3)
- (22)
- (7)
- (2)
- (4)
- (5)
- (2)
- (3)
- (26)
- (1)
- (176)
- (9)
- (17)
- (39)
- (70)
- (52)
- (9)
- (15)
- (2)
- (2)
- (8)
- (9)
- (1)
- (5)
- (2)
- (4)
- (19)
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- (7)
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- (6)
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- (3)
- (3)
- (11)
- (3)
- (62)
- (16)
- (160)
- (2)
- (1)
- (120)
- (5)
- (39)
- (2)
- (2)
- (3)
- (494)
- (2)
- (5)
- (3)
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Filtered Search Results
eMolecules 2S 4R-1-9H-FLUOREN-9-Y 1G
5000188652 2S 4R-1-9H-FLUOREN-9-Y 1G
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eMolecules 2S-4-TERT-BUTOXY-2- 9H-FL 1G
5000189755 2S-4-TERT-BUTOXY-2- 9H-FL 1G
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Chemscene CHEMSCENE
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5000577884 S-2- 9H-FLUOREN-9-YL METH 100G
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5000579628 9H-FLUOREN-9-YL METHYL 3-HY 1G
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Ambeed AMBEED
5000889452 36-BISMETHYLTHIO-9H-CARB 100MG
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eMolecules EMOLECULES INC
5000841472 S-2-9H-FLUOREN-9-YL 1G
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Aobchem AOBCHEM
5000901740 9- NAPHTHALEN-2-YL -9H-CARBAZ
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Ambeed AMBEED
5000882428 9H-DIBENZOACCARBAZOLE 5G
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Ambeed AMBEED
5000882805 9-PHENYL-9H-FLUOREN-9-OL 5G
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eMolecules 7-Fluoro-2,3,4,9-tetrahydro-1H-beta-carboline | 177858-80-9 | 250MG | Purity: 95%
Matrix Scientific | 7-Fluoro-2,3,4,9-tetrahydro-1H-beta-carboline | 250MG | 177858-80-9 | MFCD09264527
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Medchemexpress LLC PD-1/PD-L1-IN-NP19 5mg
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PD-1/PD-L1-IN-NP19 5mg
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Medchemexpress LLC Thioquinapiperifil dihydrochloride | 204077-66-7 | 99.2% | 5 MG
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Thioquinapiperifil dihydrochloride is a potent, selective, non-competitive phosphodiesterase-5 (PDE-5) inhibitor (reported IC50 0.074 nM) supplied as the dihydrochloride salt for research use in PDE-5 pharmacology.
- Potent, selective, non-competitive PDE-5 inhibitor (reported IC50 0.074 nM).
- Dihydrochloride salt form for improved handling and solubility.
- High purity suitable for research use.
- Well-defined chemical identity: formula C24H30Cl2N6OS, MW 521.51 g·mol⁻1.
- Available in small research pack sizes, including 5 mg solid and a 10 mM solution format.
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Medchemexpress LLC Nevadensin | 10176-66-6 | 344.32 | 5 MG
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Nevadensin (Lysionotin) is a natural flavonoid that acts as a selective human carboxylesterase 1 (hCE1) inhibitor with an IC50 of 2.64 μM, showing more selectivity for hCE1 than hCE2 (IC50 of 132.8 μM). It can induce apoptosis and DNA damage in cancer cells. This compound exhibits a range of pharmacological effects, including anti-inflammatory, anti-tumour, anti-hypertensive, anti-tubercular, antitussive, antioxidant, and anti-microbial activities.
- Natural flavonoid
- Selective human carboxylesterase 1 (hCE1) inhibitor
- Induces apoptosis and DNA damage in cancer cells
- Possesses anti-inflammatory activity
- Exhibits anti-tumour effects
- Has anti-hypertensive properties
- Demonstrates anti-tubercular activity
- Acts as an antitussive
- Functions as an antioxidant
- Shows anti-microbial activities
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Medchemexpress LLC Strophanthidin 25mg | 66-28-4 | 25 MG
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Strophanthidin is a naturally occurring cardiac glycoside used as a research standard and Na+/K+-ATPase modulator. It is supplied as a solid suitable for analytical, in vitro, and in vivo studies, with recommended solvents and storage guidance to maintain stability.
- Naturally occurring cardiac glycoside and Na+/K+-ATPase modulator.
- High purity suitable for analytical and biological assays.
- Offered in small research quantities for assay development.
- Soluble in ethanol; in vivo formulation protocols are provided for clear dosing solutions.
- Store solid at 4°C and protect from moisture and light to preserve integrity.
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eMolecules 370882-66-9 | tert-butyl (1S,5R)-3,6-diazabicyclo[3.2.0]heptane-6-carboxylate | Pharmablock198.266 | C10H18N2O2 | 97.000 | CC(C)(C)OC(=O)N1C[C@@H]2CNC[C@H]12 | 25mg | 586144518
tert-butyl (1S,5R)-3,6-diazabicyclo[3.2.0]heptane-6-carboxylate | Pharmablock | 370882-66-9198.266 | C10H18N2O2 | 97.000 | CC(C)(C)OC(=O)N1C[C@@H]2CNC[C@H]12 | 25mg | 586144518
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