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B220

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Category Herpes simplex Virus (HSV)
CAS 112228-65-6
Description B220 is an antiviral agent which can inhibit the growth of HSV-1, HSV-2 and human cytomegalovirus (CMV).
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Product Information

Synonyms 112228-65-6|B220|6H-Indolo(2,3-b)quinoxaline-6-ethanamine, N,N,2,3-tetramethyl-|2-(2,3-dimethylindolo[3,2-b]quinoxalin-6-yl)-N,N-dimethylethanamine|6H-Indolo[2,3-b]quinoxaline-6-ethanamine, N,N,2,3-tetramethyl-|Oprea1_679137|CHEMBL456589|SCHEMBL1581068|ZINC24937|DTXSID40920692|9-OH-B220|NSC811922|NSC-811922|HY-100272|B 220|B-220|CS-0018424|2,3-dimethyl-6(2-dimethylaminoethyl)-6h-indolo-(2,3-b)quinoxaline|2,3-Dimethyl-N,N-dimethylaminoethyl-5H-indolo(2,3-b)quinoxaline|N,N,2,3-Tetramethyl-6H-indolo[2,3-b]quinoxaline-6-ethane-1-amine|2-(2,3-dimethylindolo[3,2-b]quinoxalin-6-yl)-N,N-dimethyl-ethanamine|2,3-Dimethyl-6-(dimethylaminoethyl)-9-hydroxy-6H-indolo-(2,3-b)quinoxaline|2-(2,3-Dimethyl-6H-indolo[2,3-b]quinoxalin-6-yl)-N,N-dimethylethan-1-amine|112229-05-7
IUPAC Name 2-(2,3-dimethylindolo[3,2-b]quinoxalin-6-yl)-N,N-dimethylethanamine
Molecular Weight 318.42
Molecular Formula C20H22N4
Canonical SMILES CC1=C(C)C=C2N=C3C(N(CCN(C)C)C4=C3C=CC=C4)=NC2=C1
InChI InChI=1S/C20H22N4/c1-13-11-16-17(12-14(13)2)22-20-19(21-16)15-7-5-6-8-18(15)24(20)10-9-23(3)4/h5-8,11-12H,9-10H2,1-4H3
InChIKey FPLSGFJELWCFTH-UHFFFAOYSA-N
Boiling Point 518.8±50.0 °C at 760 mmHg
Flash Point 267.6±30.1 °C
Purity ≥99.0%
Density 1.2±0.1 g/cm3
Solubility Soluble in DMSO.
Appearance Solid
Storage Powder:
-20°C 3 years
4°C 2 years
In solvent:
-80°C 6 months
-20°C 1 months
Complexity 439
Exact Mass 318.184448
Index Of Refraction 1.650
In Vitro B220 is an antiviral agent which can inhibit the growth of HSV-1, HSV-2 and human cytomegalovirus (CMV). B220 inhibits neutrophil release of reactive oxygen species, as well as intracellular generation of reactive oxygen species. The inhibition is not achieved through direct oxygen radical scavenger activity of B220, and B220 has no immediate effects on the activity of the assembled oxidase. The neutrophil capability to phagocytose fluorescein-labeled opsonized yeast cells is reduced by B220. Cells preincubated with B220 (10 µg/mL) and then stimulated with the formylated peptide fMLP mobilize fewer C3 receptors on their surface than the control cell.
Target HSV-1; HSV-2
Vapor Pressure 0.0±1.4 mmHg at 25°C
XLogP3-AA 3.7

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