ChemicalBook > CAS DataBase List > Inflachromene
Inflachromene
- Product Name
- Inflachromene
- CAS No.
- 908568-01-4
- Chemical Name
- Inflachromene
- Synonyms
- ICM;Inflachromene;Inflachromene (ICM);5,12b-dihydro-10-hydroxy-7,7-dimethyl-2-phenyl-1H,7H-[1]benzopyrano[4,3-c][1,2,4]triazolo[1,2-a]pyridazine-1,3(2H)-dione;1H,7H-[1]Benzopyrano[4,3-c][1,2,4]triazolo[1,2-a]pyridazine-1,3(2H)-dione, 5,12b-dihydro-10-hydroxy-7,7-dimethyl-2-phenyl-
- CBNumber
- CB94200546
- Molecular Formula
- C21H19N3O4
- Formula Weight
- 377.39
- MOL File
- 908568-01-4.mol
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Inflachromene Property
- Boiling point:
- 532.6±60.0 °C(Predicted)
- Density
- 1.50±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMF:30.0(Max Conc. mg/mL);79.49(Max Conc. mM)
DMSO:30.0(Max Conc. mg/mL);79.49(Max Conc. mM)
DMSO:PBS (pH 7.2) (1:4):0.2(Max Conc. mg/mL);0.53(Max Conc. mM)
Ethanol:2.5(Max Conc. mg/mL);6.62(Max Conc. mM) - form
- A crystalline solid
- pka
- 9.65±0.40(Predicted)
- color
- White to yellow
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N-Bromosuccinimide Price
Cayman Chemical
- Product number
- 17006
- Product name
- Inflachromene
- Purity
- ≥95%
- Packaging
- 5mg
- Price
- $147
- Updated
- 2026/04/30
Cayman Chemical
- Product number
- 17006
- Product name
- Inflachromene
- Purity
- ≥95%
- Packaging
- 10mg
- Price
- $234
- Updated
- 2026/04/30
Cayman Chemical
- Product number
- 17006
- Product name
- Inflachromene
- Purity
- ≥95%
- Packaging
- 25mg
- Price
- $543
- Updated
- 2026/04/30
Cayman Chemical
- Product number
- 17006
- Product name
- Inflachromene
- Purity
- ≥95%
- Packaging
- 5mg
- Price
- $133
- Updated
- 2024/03/01
Cayman Chemical
- Product number
- 17006
- Product name
- Inflachromene
- Purity
- ≥95%
- Packaging
- 10mg
- Price
- $212
- Updated
- 2024/03/01
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Inflachromene Chemical Properties,Usage,Production
Uses
Inflachromene is a novel microglial inhibitor, which binds to HMGB1 (High Mobility Group Box 1) and HMGB2 (High mobility Group Box 2) inhibiting microglia-mediated neuroinflammation.
in vivo
Inflachromene (2-10 mg/kg; i.p. once daily for 4 days) effectively blocks LPS-mediated microglial activation[2].
Inflachromene (10 mg/kg; i.p. once daily for 30 days) significantly reduces the progression of disease, as determined by EAE clinical score[2].
Inflachromene (1 mg/kg; i.v.) exhibits long half-life (14.1±6.43 h) and moderate Vss (2.02±1.02 L/kg)[1].
Inflachromene (1 mg/kg; p.o.) exhibits high oral bioavailability (94%) and Cmax (0.59±0.16 g/mL)[1].
| Animal Model: | Male C57BL/6 mice (11 weeks; 25-30 g) are treated with LPS[2] |
| Dosage: | 2, 10 mg/kg |
| Administration: | I.p. once daily for 4 days |
| Result: | Blocked LPS-mediated microglial activation, even at a dose of 2 mg/kg. |
| Animal Model: | Sprague-Dawley (SD) rats (7 weeks; 230-250 g)[1] |
| Dosage: | 1 mg/kg (Pharmacokinetic Analysis) |
| Administration: | I.v. and p.o. administration |
| Result: | I.v.: t1/2=14.1±6.43 h; CL= 0.14±0.01 L/kg/h; Vss=2.02±1.02 L/kg. P.o.: t1/2=7.96±1.16 h; F=94%; Cmax=0.59±0.16 g/mL. |
Inflachromene Preparation Products And Raw materials
Raw materials
Preparation Products
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Inflachromene Suppliers
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