CAS 288250-47-5

1-(4-Chlorophenyl)-N-[3-cyano-4-[4-(4-morpholinyl)-1-piperidinyl]phenyl]-5-methyl-1H-pyrazole-4-carboxamide

Description:

1-(4-Chlorophenyl)-N-[3-cyano-4-[4-(4-morpholinyl)-1-piperidinyl]phenyl]-5-methyl-1H-pyrazole-4-carboxamide, with CAS number 288250-47-5, is a synthetic organic compound characterized by its complex molecular structure, which includes a pyrazole core substituted with various functional groups. This compound features a chlorophenyl group and a cyano group, contributing to its potential biological activity. The presence of a morpholine and piperidine moiety suggests that it may interact with biological targets, possibly influencing neurotransmitter systems or other cellular pathways. Its carboxamide functional group may enhance solubility and bioavailability. The compound is likely to exhibit properties such as moderate to high lipophilicity due to the aromatic rings, which can affect its pharmacokinetics. Additionally, the presence of multiple heteroatoms and functional groups indicates potential for diverse reactivity and interactions in chemical and biological contexts. Overall, this compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals targeting specific diseases or conditions.

Formula: C₂₇H₂₉ClN₆O₂

InChI: InChI=1S/C27H29ClN6O2/c1-19-25(18-30-34(19)24-5-2-21(28)3-6-24)27(35)31-22-4-7-26(20(16-22)17-29)33-10-8-23(9-11-33)32-12-14-36-15-13-32/h2-7,16,18,23H,8-15H2,1H3,(H,31,35)

InChI key: InChIKey=BWZNJVZTAWBIFG-UHFFFAOYSA-N

SMILES: C(#N)C1=C(C=CC(NC(=O)C2=C(C)N(N=C2)C3=CC=C(Cl)C=C3)=C1)N4CCC(CC4)N5CCOCC5

Synonyms:

• Y 320
• 1H-Pyrazole-4-carboxamide, 1-(4-chlorophenyl)-N-[3-cyano-4-[4-(4-morpholinyl)-1-piperidinyl]phenyl]-5-methyl-
• 1-(4-Chlorophenyl)-N-[3-cyano-4-(4-morpholin-4-ylpiperidin-1-yl)phenyl]-5-methylpyrazole-4-carboxamide
• 1-(4-Chlorophenyl)-N-[3-cyano-4-[4-(4-morpholinyl)-1-piperidinyl]phenyl]-5-methyl-1H-pyrazole-4-carboxamide
• 288250-47-5
• Y320 1-(4-Chlorophenyl)-N-[3-cyano-4-[4-(4-morpholinyl)-1-piperidinyl]phenyl]-5-methyl-1H-pyrazole-4-carboxamide
• Y-320, >=98%
• 1-(4-Chlorophenyl)-N-(3-cyano-4-(4-morpholinopiperidin-1-yl)phenyl)-5-methyl-1H-pyrazole-4-car
• Y320
• 1-(4-Chlorophenyl)-N-[3-cyano-4-[4-(4-morpholinyl)-1-piperidinyl]phenyl]-5-methyl-1H-pyrazole-4-carboxamide Y320

1-(4-chlorophenyl)-N-{3-cyano-4-[4-(morpholin-4-yl)piperidin-1-yl]phenyl}-5-methylpyrazole-4-carboxamide

CAS: 288250-47-5

Formula: C₂₇H₂₉ClN₆O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 505.0112

Ref: IN-DA002WO3

Y-320

CAS: 288250-47-5

Y-320

Purity: ≥98%

Molecular weight: 505.01g/mol

Ref: 54-BUP05475

Y-320

CAS: 288250-47-5

Formula: C₂₇H₂₉ClN₆O₂

Purity: >98.0%(HPLC)

Color and Shape: Light yellow to Brown powder to crystaline

Molecular weight: 505.02

Ref: 3B-Y0019

Y-320

CAS: 288250-47-5

Y-320 is a new phenylpyrazoleanilide immunomodulator.

Formula: C₂₇H₂₉ClN₆O₂

Purity: 98% - 99.64%

Color and Shape: Solid

Molecular weight: 505.01

Ref: TM-T1846

Y-320

CAS: 288250-47-5

Y-320 is a recombinant protein that inhibits the production of inflammatory cytokines such as IL-17a and IL-6. Y-320 also has an inhibitory effect on pro-inflammatory cells, including T cells, monocytes, and macrophages. This drug has been shown to be effective in the treatment of autoimmune diseases. Y-320's target tissue is cellular, and it is a type of monoclonal antibody. Y-320 binds to the molecule S6K1 at its activation site, thereby inhibiting the synthesis of proteins which are important for inflammatory processes. The mechanism by which Y-320 inhibits DNA replication is still unknown.

Formula: C₂₇H₂₉ClN₆O₂

Purity: Min. 95%

Molecular weight: 505.01 g/mol

Ref: 3D-NLA25047