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BOC Sciences
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1-631-485-4226; 16314854226 |
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info@bocsci.com |
| Products Intro: |
Product Name:FR-194921
CAS:202646-80-8
Purity:>98% Remarks:Reach out to us for more information about custom solutions.
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| Company Name: |
Energy Chemical
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400-0056266 |
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marketing1@energy-chemical.com |
| Products Intro: |
Product Name:FR194921 >=98% (HPLC)
CAS:202646-80-8
Purity:NULL Package:1ea;25mg;5mg Remarks:NULL
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| Company Name: |
TargetMol Chemicals Inc.
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| Tel: |
15002134094 |
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marketing@targetmol.cn |
| Products Intro: |
Product Name:FR-194921
CAS:202646-80-8
Package:25mg/RMB 10600;100mg/RMB 17500;50mg/RMB 13800
|
FR-194921 manufacturers
- FR-194921
-
- $1520.00
-
2026-04-21
- CAS:202646-80-8
- Purity:
- Supply Ability: 10g
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| | FR-194921 Basic information |
| Product Name: | FR-194921 | | Synonyms: | FR-194921;FR194921 >=98% (HPLC);3(2H)-Pyridazinone, 2-(1-methyl-4-piperidinyl)-6-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)- | | CAS: | 202646-80-8 | | MF: | C23H23N5O | | MW: | 385.46 | | EINECS: | | | Product Categories: | | | Mol File: | 202646-80-8.mol |  |
| | FR-194921 Chemical Properties |
| density | 1.29±0.1 g/cm3(Predicted) | | storage temp. | 2-8°C | | solubility | DMSO: 2mg/mL, clear (warmed) | | pka | 8.51±0.10(Predicted) | | form | Solid | | color | Off-white to light yellow | | InChI | 1S/C23H23N5O/c1-26-15-12-18(13-16-26)28-21(29)11-10-19(24-28)22-20-9-5-6-14-27(20)25-23(22)17-7-3-2-4-8-17/h2-11,14,18H,12-13,15-16H2,1H3 | | InChIKey | YHDRUTMZCJZJAL-UHFFFAOYSA-N | | SMILES | CN(CC1)CCC1N2N=C(C=CC2=O)C3=C4N(N=C3C5=CC=CC=C5)C=CC=C4 |
| WGK Germany | WGK 3 | | Storage Class | 11 - Combustible Solids |
| | FR-194921 Usage And Synthesis |
| Uses | FR194921 is a potent, selective and orally active and cross the blood-brain barrier Adenosine A1 antagonist with Ki value of 6.6, 5400 nM for A1, A2A, respectively. FR194921 shows cognitive-enhancing and anxiolytic activity[1][2]. | | Biological Activity | FR194921 is a blood-brain barrier-permeable A1R adenosine receptor antagonist. The measured Ki values of FR194921 for the human adenosine A1 receptors have been in the low nM range with no binding affinity for A2A and A3 receptors up to 1μM. It is orally active and has good bioavailability. FR194921 was used in a recent study to restore auditory cortex plasticity. Paired with sound exposure, FR194921 resulted in cortical map plasticity and improved auditory perception in adult mice. | | in vivo | FR194921 (32 mg/kg; p.o.) shows good oral bioavailability with AUC of 6.91 μg·h/mL, Cmax of 2.13 μg/mL and Tmax OF 0.63 h, BA of 60.6% in rats[1].
FR194921 (0.032, 0.1, 0.32 mg/kg; p.o.) dose-dependently attenuates the hypolocomotion induced by CPA (HY-103181)[2].
FR194921 (0.1-10 mg/kg; i.p.) significantly ameliorates scopolamine (HY-N0296)-induced memory deficits[2]. | Animal Model: | SD rats[2] | | Dosage: | 0.032, 0.1, 0.32 mg/kg | | Administration: | P.o.; administered orally 25 min prior to intraperitoneal administration of CPA (0.056 mg/kg; i.p.) | | Result: | Dose-dependently attenuated the hypolocomotion induced by CPA with an ED50 value of 0.08 mg/kg and statistical significance at 0.32 mg/kg. |
| Animal Model: | SD rats[2] | | Dosage: | 0.1, 0.32, 1, 3.2, 10 mg/kg | | Administration: | I.p.; Scopolamine (HY-N0296)(1 mg/kg, i.p.) | | Result: | Significant cognitive enhanced following scopolamine-induced memory deficits in rats. |
| | IC 50 | A1R: 6.6 nM (Ki); A2AR: 5400 nM (Ki) | | References | [1] Kuroda S, et al. Design, synthesis and biological evaluation of a novel series of potent, orally active adenosine A1 receptor antagonists with high blood-brain barrier permeability. Chem Pharm Bull (Tokyo). 2001 Aug;49(8):988-98. DOI:10.1248/cpb.49.988
[2] Maemoto T, et al. Pharmacological characterization of FR194921, a new potent, selective, and orally active antagonist for central adenosine A1 receptors. J Pharmacol Sci. 2004 Sep;96(1):42-52. DOI:10.1254/jphs.fp0040359 |
| | FR-194921 Preparation Products And Raw materials |
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