5972-45-2
5972-45-2
Chemical Structure
JPC0323
- CAS No.: 5972-45-2
- Formula:C22H43NO4
- Molecular Weight:385.58
InChIKey: JLFKELVBPUSMGW-KTKRTIGZSA-N
SMILES: O=C(NC(CO)(CO)CO)CCCCCCC/C=C\CCCCCCCC
Biological Activity: JPC0323 is a dual 5-HT2C/5-HT2A receptor positive allosteric modulator. JPC0323 has on-target properties, acceptable plasma exposure and brain penetration. JPC0323 can be used for the research of neurological disease[1].
| Cat. No. | Nom du produit | Pureté | Description | Pricing | |||||||||||||||||||
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JPC0323 | JPC0323 is a dual 5-HT2C/5-HT2A receptor positive allosteric modulator. JPC0323 has on-target properties, acceptable plasma exposure and brain penetration. JPC0323 can be used for the research of neurological disease. | |||||||||||||||||||||
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Oleoylethanolamide (Standard) | 99.86% | Oleoylethanolamide (Standard) is the analytical standard of Oleoylethanolamide. This product is intended for research and analytical applications. Oleoylethanolamide is a high affinity endogenous PPAR-α agonist, which plays an important role in the treatment of obesity and arteriosclerosis. | ||||||||||||||||||||
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N-Oleoyl glycine | 99.0% | N-Oleoyl glycine is a lipoamino acid, which stimulates adipogenesis associated with activation of CB1 receptor and Akt signaling pathway in 3T3-L1 adipocyte. | ||||||||||||||||||||
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Oleoyl ethyl amide | 99.9% | Oleoyl ethyl amide (N-Ethyloleamide) is a fatty acid amide hydrolase (FAAH) inhibitor that can cross the blood-brain barrier. Oleoyl ethyl amide enhances endogenous cannabinoid signaling by inhibiting FAAH, and via CB1/CB2 and TRPV1 receptor mediation, thereby modulating peripheral sensory and motor nerve transmission. Oleoyl ethyl amide can be used in research on overactive bladder and premature ejaculation. | ||||||||||||||||||||
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N-Oleoyl serinol | 98.36% | N-Oleoyl serinol is a ceramide analog that can be used in stem cell therapy to prevent stem cells from developing into teratomas. N-Oleoyl serinol induces apoptosis in residual pluripotent embryoid body-derived cells (EBCs), prevents teratoma formation, and enriches EBC cells that undergo neural differentiation after transplantation. | ||||||||||||||||||||
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N-Oleoyl-L-serine | 99.72% | N-Oleoyl-L-Serine is an endogenous amide of long-chain fatty acids with ethanolamine (N-acyl amides). N-Oleoyl-L-Serine is a lipid regulator of bone remodeling and stimulates osteoclast apoptosis. N-Oleoyl-L-Serine can be used for antiosteoporotic drug discovery development. | ||||||||||||||||||||
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AM3102 | 98.0% | AM3102 is an oleoylethanolamide (OEA) analog. AM3102 is an endogenous high-affinity PPAR-alpha agonist. AM3102 resists enzymatic hydrolysis, activates PPAR-alpha with high potency in vitro, and persistently reduces feeding when administered in vivo either parenterally or orally. | ||||||||||||||||||||
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Oleic acid diethanolamide | Oleic acid diethanolamide (OADA) is a non-ionic, biodegradable surfactant. Oleic acid diethanolamide reduces the surface tension of water, emulsifies free water in diesel fuel to form a stable emulsion, and can be loaded onto sulfonated polystyrene nanoparticles to enhance oil recovery. Oleic acid diethanolamide is one of the nematicidal secondary metabolites produced by Aspergillus flavus. Oleic acid diethanolamide can be used in studies related to biological control of root-knot nematodes, enhanced oil recovery, and diesel fuel emulsion stabilization. | |||||||||||||||||||||
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Docosaenoyl ethanolamide | Docosaenoyl ethanolamide (N-(2-Hydroxyethyl)-13Z-docosenamide) is one of a fatty N-acyl ethanolamines. Ethanolamines can be detected at relatively high levels in rat cerebrospinal fluid. | |||||||||||||||||||||
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C17:1 Anandamide | C17:1 Anandamide is an anandamide. | |||||||||||||||||||||
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C18:1 Anandamide | C18:1 Anandamide is an anandamide. | |||||||||||||||||||||
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