Quinolines and derivatives
eMolecules 74124-79-1 | N,N'-Disuccinimidyl carbonate | Chem-Impex | MFCD00009767 | 256.170 | C9H8N2O7 | 99.000 | O=C(ON1C(=O)CCC1=O)ON1C(=O)CCC1=O | 5kg | 342449122
N,N'-Disuccinimidyl carbonate | Chem-Impex | 74124-79-1 | MFCD00009767 | 256.170 | C9H8N2O7 | 99.000 | O=C(ON1C(=O)CCC1=O)ON1C(=O)CCC1=O | 5kg | 342449122
eMolecules 1170979-26-6 | METHYL 6-AMINOQUINOLINE-3-CARBOXYLATE | AstaTech | MFCD18073413 | 202.213 | C11H10N2O2 | 95.000 | COC(=O)c1cnc2ccc(N)cc2c1 | 1g | 449771392
METHYL 6-AMINOQUINOLINE-3-CARBOXYLATE | AstaTech | 1170979-26-6 | MFCD18073413 | 202.213 | C11H10N2O2 | 95.000 | COC(=O)c1cnc2ccc(N)cc2c1 | 1g | 449771392
Medchemexpress LLC Azido-PEG7-amine | 1333154-77-0 | MFCD13185016 | >98.0% | 394.46 g/mol | C16H34N4O7 | 50 MG
Azido-PEG7-amine is a bifunctional polyethylene glycol (PEG) linker bearing an azide and a primary amine terminus. It is used as a click-chemistry building block and as a linker in antibody-drug conjugate (ADC) and PROTAC synthesis.
- Bifunctional azide and primary amine termini suitable for conjugation.
- PEG7 spacer provides a short, flexible linker (seven ethylene glycol units).
- Compatible with copper-catalyzed azide-alkyne cycloaddition and strain-promoted click reactions.
- High reported purity, typically greater than 98%.
- Supplied in small laboratory pack sizes for research use.
Medchemexpress LLC Amino-PEG8-amine | 82209-36-7 | 98.0% | 500 MG
Amino-PEG8-amine is a PEG-based (8 units) PROTAC linker used in the synthesis of PROTACs. PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- Appears as liquid
- Color is colorless to light yellow
- Molecular weight: 412.52
- Molecular formula: C18H40N2O8
- CAS number: 82209-36-7
- Purity: 98.0%
- Store at 4°C, protected from light
- In solvent, store at -80°C for 6 months or -20°C for 1 month (protected from light)
- Soluble in DMSO at 100 mg/mL
eMolecules 5622-36-6 | methyl 2-(quinolin-6-yl)acetate | Pharmablock | MFCD04038669 | 201.225 | C12H11NO2 | 97.000 | COC(=O)Cc1ccc2ncccc2c1 | 2.5g | 686950173
methyl 2-(quinolin-6-yl)acetate | Pharmablock | 5622-36-6 | MFCD04038669 | 201.225 | C12H11NO2 | 97.000 | COC(=O)Cc1ccc2ncccc2c1 | 2.5g | 686950173
eMolecules 58794-09-5 | 7-bromoisoquinoline | AA Blocks LLC | MFCD07368661 | 208.058 | C9H6BrN | 0.000 | Brc1ccc2ccncc2c1 | 25g | 410166202
7-bromoisoquinoline | AA Blocks LLC | 58794-09-5 | MFCD07368661 | 208.058 | C9H6BrN | 0.000 | Brc1ccc2ccncc2c1 | 25g | 410166202
Medchemexpress LLC Azido-PEG23-amine | 2172677-19-7 | 99.93% | C48H98N4O23 | 50 MG
Azido-PEG23-amine is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It functions as a click chemistry reagent, possessing an azide group that enables various cycloaddition reactions.
- PEG-based PROTAC linker
- Click chemistry reagent
- Contains an azide group
- Undergoes copper-catalyzed azide-alkyne cycloaddition (CuAAc) reaction with alkyne groups
- Participates in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups
Medchemexpress LLC 5(6)-Carboxy-2',7'-dichlorofluorescein | 111843-78-8 | 99.0% | 100 MG
5(6)-Carboxy-2',7'-dichlorofluorescein is an ideal substrate for MRP2 vesicular transport assay, possessing excellent detection and transport properties.
- Ideal substrate for MRP2 vesicular transport assay
- Excellent detection and transport properties
Medchemexpress LLC Quin C1 | 786706-21-6 | 98.5% | 445.51 | 500 UG
Quin C1 is a highly specific and potent agonist for formyl peptide receptor 2 (FPR2/ALX). It significantly reduces neutrophil and lymphocyte counts in BALF, diminishes expression of TNF-α, IL-1β, KC, and TGF-β1, and decreases collagen deposition in lung tissue.
- Highly specific and potent agonist for formyl peptide receptor 2 (FPR2/ALX)
- Significantly reduces neutrophil and lymphocyte counts in BALF
- Diminishes expression of TNF-α, IL-1β, KC, and TGF-β1
- Decreases collagen deposition in lung tissue
- Potential for research into lung injury
eMolecules 58794-09-5 | 7-Bromoisoquinoline | Apollo Scientific - Building Blocks | MFCD07368661 | 208.058 | C9H6BrN | 95.000 | Brc1ccc2ccncc2c1 | 250mg | 553346418
7-Bromoisoquinoline | Apollo Scientific - Building Blocks | 58794-09-5 | MFCD07368661 | 208.058 | C9H6BrN | 95.000 | Brc1ccc2ccncc2c1 | 250mg | 553346418
Medchemexpress LLC 5-Bromoquinoline | 4964-71-0 | 208.06 | 10 G
5-Bromoquinoline is a biochemical reagent and organic compound used in life science research and for the manufacture of substances. It is intended for laboratory use only.
- Biochemical reagent for life science research
- Used in the manufacture of substances
- Solid appearance, white to light brown color
- Purity of 98.1%
- Molecular weight of 208.06
- Stable under recommended storage conditions
- Melting point 50-52°C
- Boiling point 295.9°C
Medchemexpress LLC Peg-bis-amine (MW 2000) | 24991-53-5 | 99.4% | (C2H4O)nC4H12N2O | 250 MG
PEG-bis-amine (Poly(ethylene glycol)-bis-amine) (MW 2000) is a PEG-based PROTAC linker. It is used in the synthesis of PROTACs, which are molecules designed to exploit the intracellular ubiquitin-proteasome system for selective degradation of target proteins.
- Can be used in the synthesis of PROTACs
- PROTACs contain two different ligands connected by a linker
- Ligands are for an E3 ubiquitin ligase and a target protein
- PROTACs exploit the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
TARGETMOL CHEMICALS INC Fluoxetine 200MG
Also available in 1 mL, 10 mg, 25 mg, 50 mg, 100 mg, 500 mg and bulk. Please contact Fisher for quotes. Fluoxetine (LY-110140) is a highly specific serotonin uptake inhibitor and selective 5-hydroxytryptamine (5-HT) reuptake inhibitor. Fluoxetine has antidepressant activity. Purity 99.65%
Medchemexpress LLC Tirapazamine | 27314-97-2 | 99.0% | 178.15 | 200 MG
Tirapazamine (SR259075) is an anticancer agent that shows selective cytotoxicity for hypoxic cells in solid tumors, thereby inducing single- and double-strand breaks in DNA, base damage, and cell death. It is an anticancer and bioreductive agent that can enhance the cytotoxic effects of ionizing radiation in hypoxic cells.
- Selective cytotoxicity for hypoxic cells
- Induces single- and double-strand breaks in DNA
- Induces base damage and cell death
- Enhances cytotoxic effects of ionizing radiation in hypoxic cells