1. Home
  2. Fananserin

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Fananserin

Fc1ccc(cc1)N1CCN(CC1)CCCN1c2cccc3c2c(S1(=O)=O)ccc3 Request for Quotation
Chemical Name: Fananserin
CAS Number: 127625-29-0
Product Number: AG000X89(AGN-PC-0JL457)
Synonyms:
MDL No: MFCD00866648
Molecular Formula: C23H24FN3O2S
Molecular Weight: 425.5190

Identification/Properties

Computed Properties
Molecular Weight:
425.522g/mol
XLogP3:
4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
5
Exact Mass:
425.157g/mol
Monoisotopic Mass:
425.157g/mol
Topological Polar Surface Area:
52.2A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
683
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Fananserin is a potent and selective serotonin receptor antagonist that is utilized in chemical synthesis for its unique pharmacological properties. Its ability to inhibit serotonin receptors makes it a valuable tool in the development of new pharmaceutical compounds, particularly those targeting the central nervous system. In chemical reactions, Fananserin can act as a catalyst or a reagent to facilitate the synthesis of various organic compounds. Its role in mediating serotonin neurotransmission also offers potential applications in the study of neurological disorders and mental health conditions. In the field of medicinal chemistry, Fananserin serves as a key building block for designing novel drugs with improved efficacy and reduced side effects. By incorporating Fananserin into synthetic pathways, researchers can access a diverse range of molecular scaffolds that have the potential to lead to the discovery of innovative therapeutic agents.