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| Product | Description | |
|---|---|---|
| SB-269970 | SB-269970 is a potent, selective and brain-penetrant 5-HT7 receptor antagonist with a pK i of 8.3. SB-269970 exhibits >50-fold selectivity against other 5-HT receptors [1] [2]. Uses: Scientific research. Group: Signaling pathways. CAS No. 201038-74-6. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-15370. |  |
| SB-269970 | SB-269970 is a selective 5-HT7 receptor antagonist (pKi of 8.3) with >50-fold selectivity against other receptors, on amphetamine and ketamine-induced hyperactivity and prepulse inhibition (PPI) deficits. Synonyms: 3-[(2R)-2-[2-(4-methylpiperidin-1-yl)ethyl]pyrrolidin-1-yl]sulfonylphenol3-(2-(2-(4-methylpiperidin-1-yl)ethyl)pyrrolidine-1-sulfonyl)phenolSB 269970; SB269970SB-269970. Grades: >98 %. CAS No. 201038-74-6. Molecular formula: C18H28N2O3S. Mole weight: 352.49. |  |
| SB-269970 hydrochloride | powder, ?98% (HPLC). Group: Fluorescence/luminescence spectroscopy. |  |
| SB-269970 hydrochloride | SB269970 HCl is a hydrochloride salt form of SB-269970, which is a 5-HT7 receptor antagonist with pKi of 8.3, exhibits >50-fold selectivity against other receptors. Synonyms: SB-269970 hydrochloride; SB 269970 hydrochloride; SB269970 hydrochloride. Grades: >98%. CAS No. 261901-57-9. Molecular formula: C18H28N2O3S.HCl. Mole weight: 388.95. | |
| SB-269970 hydrochloride | SB-269970 hydrochloride is a potent, selective and brain-penetrant 5-HT7 receptor antagonist with a pK i of 8.3. SB-269970 hydrochloride exhibits >50-fold selectivity against other 5-HT receptors [1] [2]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: SB-269970A. CAS No. 261901-57-9. Pack Sizes: 10 mM * 1 mL; 5 mg; 10 mg; 25 mg; 50 mg. Product ID: HY-15370A. | |
| SB-269970 Hydrochloride (5-HT7 Serotonin Receptor Antagonist, SB-269970, SB 26,970, SB 26,970) | A selective 5-HT7 receptor antagonist. Extremely potent in vivo and in vitro. Chronic or acute (even single dose) administration of SB269970 induces functional desensitization of the 5-HT7 receptor system, which precedes changes in the receptor density. This mechanism may be responsible for the rapid antidepressant-like effect of the 5-HT7 antagonist in animal models. SB-269970 is an analogue of SB-258719 and has been shown to have at least 100 fold selectivity versus all other 5-HT receptor subtypes except the human 5-HT5A receptor (pKi values are 8.9, 7.2 and 6.0 for 5-HT7A, 5-HT5A and 5-HT1B). Group: Biochemicals. Grades: Highly Purified. CAS No. 261901-57-9. Pack Sizes: 10mg. Molecular Formula: C??H??N?O?S·HCl. US Biological Life Sciences. |  Worldwide |
| LP-44 Hydrochloride | A potent agonist of the 5-HT7 serotonin receptor (Ki= 0.22nM) with good selectivity against other 5-HT receptors (5-HT1A Ki = 52.7nM, 5-HT1B Ki = 60nM). Often used in conjuction with the selective 5-HT7 receptor antagonist, SB-269970. Group: Biochemicals. Grades: Highly Purified. CAS No. 824958-12-5. Pack Sizes: 10mg. Molecular Formula: C??H??ClN?OS. US Biological Life Sciences. | Worldwide |
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