JJKK 048
- Product Name
- JJKK 048
- CAS No.
- 1515855-97-6
- Chemical Name
- JJKK 048
- Synonyms
- JJKK 048;JJKK-048 >=98% (HPLC);JJKK 048, 10 mM in DMSO;inhibit,JJKK-048,JJKK048,MAGL,Inhibitor,Monoacylglycerol lipase,JJKK 048;4-[Bis(1,3-benzodioxol-5-yl)methyl]-1-piperidinyl]-1H-1,2,4-triazol-1-yl-methanone;Methanone, [4-[bis(1,3-benzodioxol-5-yl)methyl]-1-piperidinyl]-1H-1,2,4-triazol-1-yl-;(4-(Bis(benzo[d][1,3]dioxol-5-yl)methyl)piperidin-1-yl)(1H-1,2,4-triazol-1-yl)methanone
- CBNumber
- CB43167160
- Molecular Formula
- C23H22N4O5
- Formula Weight
- 434.44
- MOL File
- 1515855-97-6.mol
JJKK 048 Property
- Boiling point:
- 615.9±65.0 °C(Predicted)
- Density
- 1.52±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- Soluble to 100 mM in DMSO
- form
- Powder
- pka
- 1.70±0.10(Predicted)
- color
- White to off-white
- InChI
- 1S/C23H22N4O5/c28-23(27-12-24-11-25-27)26-7-5-15(6-8-26)22(16-1-3-18-20(9-16)31-13-29-18)17-2-4-19-21(10-17)32-14-30-19/h1-4,9-12,15,22H,5-8,13-14H2
- InChIKey
- CLSNATLUIXZPMV-UHFFFAOYSA-N
- SMILES
- O=C(N1N=CN=C1)N2CCC(C(C3=CC(OCO4)=C4C=C3)C5=CC=C(OCO6)C6=C5)CC2
Safety
- WGK Germany
- WGK 3
- Storage Class
- 11 - Combustible Solids
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P280Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352IF ON SKIN: wash with plenty of soap and water.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
P332+P313IF SKIN irritation occurs: Get medical advice/attention.
P337+P313IF eye irritation persists: Get medical advice/attention.
N-Bromosuccinimide Price
- Product number
- SML1830
- Product name
- JJKK-048
- Purity
- ≥98% (HPLC)
- Packaging
- 5MG
- Price
- $125
- Updated
- 2026/04/30
- Product number
- SML1830
- Product name
- JJKK-048
- Purity
- ≥98% (HPLC)
- Packaging
- 25MG
- Price
- $511
- Updated
- 2026/04/30
- Product number
- 5206
- Product name
- JJKK048
- Purity
- ≥98%(HPLC)
- Packaging
- 10
- Price
- $219
- Updated
- 2021/12/16
- Product number
- J212008
- Product name
- JJKK048
- Packaging
- 2.5mg
- Price
- $195
- Updated
- 2021/12/16
- Product number
- 255553
- Product name
- JJKK 048
- Packaging
- 10mg
- Price
- $475
- Updated
- 2021/12/16
JJKK 048 Chemical Properties,Usage,Production
Uses
JJKK 048 inhibits monoacylglycerol lipase by terminating signaling pathway of 2-arachidonoylglycerol in mouse brain and human melanoma cell proteome. JJKK 048 can be classified as a MAGL inhibitor that has therapeutic potential for the treatment of cancers.
Biological Activity
JJKK-048 is a cell penetrant ultrapotent and highly selective inhibitor of monoacylglycerol lipase (MAGL) th at exhibits a low cross-reactivity with other endocannabinoid targets. JJKK-048 is an irreversible inhibitor th at binds to the active site S122.
in vivo
JJKK 048 (0.1-4 mg/kg; i.p.; single dose; acute administration) potently inhibits MAGL and elevates brain 2-Arachidonoylglycerol (2-AG) (HY-W011051) levels in male C57Bl/6J mice[2].
JJKK 048 (0.5-2 mg/kg; i.p.; single dose; acute administration) inhibits MAGL in peripheral tissues (liver, spleen, heart, and skeletal muscle) with some off - target effects in mouse[2].
JJKK 048 (0.5 mg/kg; i.p.; single dose; acute administration) promotes significant analgesia in a writhing test in male Albino Swiss mice without causing cannabimimetic side effects[2].
JJKK 048 (1-2 mg/kg; i.p.; single dose; acute administration) induces analgesia both in the writhing test and in the tail - immersion test, as well as hypomotility and hyperthermia, but not catalepsy in male Albino Swiss mice[2].
| Animal Model: | Male C57Bl/6J mice (8 weeks old, weight 20-26 g)[2] |
| Dosage: | 0.1 mg/kg, 0.5 mg/kg, 1 mg/kg, 2 mg/kg, 4 mg/kg, (dissolved in 5% (v/v) dimethylsulfoxide (DMSO) in gently heated 10% (w/v) HP-β-CD (HY-101103)) |
| Administration: | i.p., single dose |
| Result: | Revealed a dose-dependent blockade of MAGL in the brain. Increased brain 2-AG levels in a dose-dependent manner, while brain AEA levels remained unaffected. |
| Animal Model: | Male Albino Swiss mice (weight 20-30 g), tetrad test model for cannabimimetic effects[2] |
| Dosage: | 0.5 mg/kg, 1 mg/kg, 2 mg/kg (dissolved in 5% (v/v) DMSO in gently heated 10% (w/v) HP-β-CD (HY-101103)) |
| Administration: | i.p., single dose |
| Result: | Caused significant reduction in the writhing episodes of mice in the writhing test, indicating an antinociceptive effect. |
storage
Store at -20°C
JJKK 048 Preparation Products And Raw materials
Raw materials
Preparation Products
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