CYM 5520

Modify Date: 2024-01-08 16:39:51

CYM 5520 Structure
CYM 5520 structure
Common Name CYM 5520
CAS Number 1449747-00-5 Molecular Weight 345.395
Density 1.2±0.1 g/cm3 Boiling Point 580.5±50.0 °C at 760 mmHg
Molecular Formula C21H19N3O2 Melting Point N/A
MSDS USA Flash Point 304.9±30.1 °C
Symbol GHS05 GHS06
GHS05, GHS06
Signal Word Danger

 Use of CYM 5520


CYM-5520 is a selective and allosteric sphingosine 1-phosphate receptor 2 (S1PR2) agonist with an EC50 of 480 nM. CYM-5520 does not activate S1PR1, S1PR3, S1PR4 and S1PR5 receptors. CYM-5520 can co-bind in the S1PR2 receptor with S1P. CYM-5520 can be used for osteoporosis research[1][2].

 Names

Name 1-[2-(1-Benzyl-2,5-dimethyl-1H-pyrrol-3-yl)-2-oxoethyl]-6-oxo-1,6-dihydro-3-pyridinecarbonitrile
Synonym More Synonyms

 CYM 5520 Biological Activity

Description CYM-5520 is a selective and allosteric sphingosine 1-phosphate receptor 2 (S1PR2) agonist with an EC50 of 480 nM. CYM-5520 does not activate S1PR1, S1PR3, S1PR4 and S1PR5 receptors. CYM-5520 can co-bind in the S1PR2 receptor with S1P. CYM-5520 can be used for osteoporosis research[1][2].
Related Catalog
In Vitro CYM-5520 (EC50 of 1.6 μM) is a full agonist for wild type S1PR2. Stimulation of cells expressing the triple mutant S1PR2 with S1P does not elicit a rise in luciferase activity, whereas the CYM-5520 is an agonist with an EC50 of 1.5 μM[1].
In Vivo CYM-5520 (10 mg/kg; i.p.; 5 consecutive days per week; for 6 weeks) treatment clearly increases long bone and vertebral bone mass in osteopenic ovariectomized mice. CYM-5520 also increases osteoblast number, osteoid surface and alkaline phosphatase, and plasma concentrations of the osteoanabolic marker procollagen I C-terminal propeptide are also elevated[2]. Animal Model: Ovariectomized 12 weeks old C57Bl6J mice[2] Dosage: 10 mg/kg Administration: i.p.; 5 consecutive days per week; for 6 weeks Result: Corrected ovariectomy-induced osteopenia in mice by inducing new bone formation.
References

[1]. Hideo Satsu, et al. A sphingosine 1-phosphate receptor 2 selective allosteric agonist. Bioorg Med Chem. 2013 Sep 1;21(17):5373-82.

[2]. Sarah Weske, et al. Agonist-induced activation of the S1P receptor 2 constitutes a novel osteoanabolic therapy for the treatment of osteoporosis in mice. Bone. 2019 Aug;125:1-7.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 580.5±50.0 °C at 760 mmHg
Molecular Formula C21H19N3O2
Molecular Weight 345.395
Flash Point 304.9±30.1 °C
Exact Mass 345.147736
LogP 2.52
Vapour Pressure 0.0±1.6 mmHg at 25°C
Index of Refraction 1.611
Storage condition 2-8°C

 Safety Information

Symbol GHS05 GHS06
GHS05, GHS06
Signal Word Danger
Hazard Statements H301-H318
Precautionary Statements P280-P301 + P310-P305 + P351 + P338
Risk Phrases 25-41
Safety Phrases 26-39-45
RIDADR UN 2811 6.1 / PGIII

 Synonyms

3-Pyridinecarbonitrile, 1-[2-[2,5-dimethyl-1-(phenylmethyl)-1H-pyrrol-3-yl]-2-oxoethyl]-1,6-dihydro-6-oxo-
MFCD28100815
1-[2-(1-Benzyl-2,5-dimethyl-1H-pyrrol-3-yl)-2-oxoethyl]-6-oxo-1,6-dihydro-3-pyridinecarbonitrile
CYM-5520
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Price: ¥1300/10 mM * 1 mL in DMSO

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