Quinolines and derivatives

Aromatic organic heterocyclic compounds that contain a benzene ring fused with a six-membered ring that contains one nitrogen atom and five carbon atoms. Includes compounds that are derived from quinolines.

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1,831 – 1,845 of 4,235 results

1,831

Ambeed 2 2 6Trimethyl4H1 3dioxin4one

2,2,6-Trimethyl-4H-1,3-dioxin-4-one, 5394-63-8, 95%

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1,832

Ambeed 1R 2R Cyclohexane1 2diamine

(1R,2R)-Cyclohexane-1,2-diamine, 20439-47-8, 96%

Pricing & Availability

1,833

TARGETMOL CHEMICALS INC JH-RE-06 5MG

Also available in 1 mg 10 mg 25 mg 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. JH-RE-06 disrupts mutagenic translesion synthesis (TLS) by preventing the recruitment of mutagenic POL(zeta). JH-RE-06 is an effective REV1-REV7 interface inhibitor (IC50=0.78 uM; Kd=0.42 uM) which targets REV1 that interacts with the REV7 subunit of POL(zeta). JH-RE-06 also improves chemotherapy. purity: 99%

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1,834

Medchemexpress LLC Azatadine (dimaleate) | 3978-86-7 | 99.85% | 200 MG

Azatadine dimaleate is an inhibitor of histamine and cholinergic with an IC50 of 6. It also exhibits antiserotonin activity and can be used in research on perennial allergic rhinitis.

Inhibitor of histamine and cholinergic
Exhibits antiserotonin activity
Can be studied in research on perennial allergic rhinitis
Targets histamine receptor
Involves GPCR/G protein, immunology/inflammation, and neuronal signaling pathways

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1,835

Chemscene CHEMSCENE

5000578733 PDE5-IN-7 25G

Pricing & Availability

1,836

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 | 100g | 112443063

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 | 100g | 112443063

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1,837

Ambeed 7Bromo1 2dihydroisoquinolin3 4

7-Bromo-1,2-dihydroisoquinolin-3(4H)-one, 943751-93-7, 95%

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1,838

Ambeed AMBEED

5000848651 TRIMETHYL 2-TETRAHYDROP 5G

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1,839

Apexbio Technology LLC 17-AAG (KOS953) 75747-14-7 200mg

17-AAG (KOS953) is a synthetic derivative of geldanamycin that inhibits heat shock protein 90 (HSP90) It acts by binding to HSP90 causing destabilization of client proteins including HER2 Raf-1 p53 and components of MAPK signaling pathways Reported IC50 for 17-AAG in BT474 cells is approximately 6 nM Its biological activity has been investigated broadly including in multiple myeloma breast cancer thyroid cancer Hodgkin lymphoma and melanoma cellular models Ongoing studies explore 17-AAG both as monotherapy and in combination with agents like bortezomib or trastuzumab for addressing treatment-resistant cancer cell lines Currently 17-AAG is evaluated in Phase II clinical trials