SLF1081851
CAS No. 2763730-97-6
SLF1081851( —— )
Catalog No. M35512 CAS No. 2763730-97-6
SLF1081851 is a Spns2 inhibitor. SLF1081851 inhibits S1P release with IC50 of 1.93 μM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 78 | Get Quote |
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| 5MG | 116 | Get Quote |
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| 10MG | 187 | Get Quote |
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| 25MG | 388 | Get Quote |
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| 50MG | 578 | Get Quote |
|
| 100MG | 804 | Get Quote |
|
| 500MG | Get Quote | Get Quote |
|
| 1G | Get Quote | Get Quote |
|
Biological Information
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Product NameSLF1081851
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NoteResearch use only, not for human use.
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Brief DescriptionSLF1081851 is a Spns2 inhibitor. SLF1081851 inhibits S1P release with IC50 of 1.93 μM.
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DescriptionSLF1081851 is a Spns2 inhibitor, inhibits S1P release (IC50=1.93 μM). SLF1081851 plays a key role in development and immune system.
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In Vitro——
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In VivoAnimal Model:C57BL/6 mice Dosage:20 mg/kg Administration:Intraperitoneal injection; blood was drawn 4 h postdose Result:Significantly decreased circulating lymphocyte count and plasma S1P concentration.Animal Model:Sprague Dawley mice (4-week-old) Dosage:10 mg/kg Administration:Intraperitoneal injection; single dose; measured at 0, 0.5, 1, 2, 4, 6, and 24 h postdose Result:Reached a maximum concentration of 5 μM in blood at 2 h with drug levels sustained at ≥ 2 μM for at least 24 h, proved a half-life of over 8 h in rats. The appearance of SPNS2-IN-1 in circulation correlated with a maximal decrease in lymphocyte count at 4 h (25% lower compared to time =0).
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorLPL Receptor
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Research Area——
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Indication——
Chemical Information
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CAS Number2763730-97-6
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Formula Weight343.51
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Molecular FormulaC21H33N3O
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Purity>98% (HPLC)
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SolubilityIn Vitro:?Ethanol : 10 mg/mL (29.11 mM; Ultrasonic)
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SMILESCCCCCCCCCCc1ccc(cc1)-c1noc(CCCN)n1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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BAY1217389
BAY 1217389 is an effective and selective inhibitor of the monopolar spindle 1 (MPS1) kinase (IC50<10 nM).
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CRSP-1
Endogenous central calcitonin (CT) receptor agonist that stimulates cAMP formation at a potency 350-fold greater than CT (ED50 values are 0.2 and 71 nM respectively). Displays no activity at calcitonin-gene related peptide (CGRP) and adrenomedullin receptors. Inhibits formation of multinuclear osteoclasts with similar efficacy to CT in vitro. Suppresses food intake and increases body temperature in free-feeding rats, and significantly decreases plasma calcium levels in vivo.
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DIM-C-pPhOCH3
DIM-C-pPhOCH3 is a Nerve Growth Factor-Induced Bα (NGFI-Bα, Nur77) agonist.
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