Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More
  1. Home
  2. Products
  3. Chemicals
  4. Organic compounds
  5. Organoheterocyclic compounds
  6. Quinolines and derivatives
  7. OPC 21268, Tocris Bioscience™

OPC 21268, Tocris Bioscience™

Catalog Number 392450
Click to view available options
Quantity:
10 mg
50 mg
This item is not returnable. View return policy
131631-89-5
C26H31N3O4
449.551
KSNUCNRMDYJBKT-UHFFFAOYSA-N
fuscoside, 1-1-4-3-acetylaminopropoxy benzoyl-4-piperidyl-3,4-dihydro-2 1h-quinolinone, opc-21268 hydrate, n-3-4-4-2-oxo-3,4-dihydroquinolin-1-yl piperidine-1-carbonyl phenoxy propyl acetamide, acetamide, n-3-4-4-3,4-dihydro-2-oxo-1 2h-quinolinyl-1-piperidinyl carbonyl phenoxy propyl, n-3-4-4-2-oxo-3,4-dihydroquinolin-1 2h-yl piperidine-1-carbonyl phenoxy propyl acetamide, acmc-20mu6h, d03qhk, d08oro, n-3-4-4-2-oxo-3,4-dihydro-2h-quinolin-1-yl-piperidine-1-carbonyl-phenoxy-propyl-acetamide
114904
N-[3-[4-[4-(2-oxo-3,4-dihydroquinolin-1-yl)piperidine-1-carbonyl]phenoxy]propyl]acetamide
CC(=O)NCCCOC1=CC=C(C=C1)C(=O)N2CCC(CC2)N3C(=O)CCC4=CC=CC=C43
This item is not returnable. View return policy
131631-89-5
C26H31N3O4
449.551
KSNUCNRMDYJBKT-UHFFFAOYSA-N
fuscoside, 1-1-4-3-acetylaminopropoxy benzoyl-4-piperidyl-3,4-dihydro-2 1h-quinolinone, opc-21268 hydrate, n-3-4-4-2-oxo-3,4-dihydroquinolin-1-yl piperidine-1-carbonyl phenoxy propyl acetamide, acetamide, n-3-4-4-3,4-dihydro-2-oxo-1 2h-quinolinyl-1-piperidinyl carbonyl phenoxy propyl, n-3-4-4-2-oxo-3,4-dihydroquinolin-1 2h-yl piperidine-1-carbonyl phenoxy propyl acetamide, acmc-20mu6h, d03qhk, d08oro, n-3-4-4-2-oxo-3,4-dihydro-2h-quinolin-1-yl-piperidine-1-carbonyl-phenoxy-propyl-acetamide
114904
N-[3-[4-[4-(2-oxo-3,4-dihydroquinolin-1-yl)piperidine-1-carbonyl]phenoxy]propyl]acetamide
CC(=O)NCCCOC1=CC=C(C=C1)C(=O)N2CCC(CC2)N3C(=O)CCC4=CC=CC=C43

Description

Orally active vasopressin V1 antagonist

Nonpeptide vasopressin V1 receptor antagonist. Displays greater affinity for rat V1 than human V1 (Ki values are 25 and 8800 nM respectively). Exhibits 1000-fold selectivity for V1 receptors over V2 receptors. Orally active.
Quantity 50 mg
Formula Weight 449.54
Percent Purity >98%
Chemical Name or Material OPC 21268

Safety and Handling

Recommended Storage Store at +4°C
Provide Content Correction

We continue to work to improve your shopping experience and your feedback regarding this content is very important to us. Please use the form below to provide feedback related to the content on this product.

Product Title

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.

Cancel Submit