MK-6892
- Product Name
- MK-6892
- CAS No.
- 917910-45-3
- Chemical Name
- MK-6892
- Synonyms
- MK-6892;CS-2425;MK 6892;MK6892;HCAR2,PUMA-G,MK-6892,HM74A,HCA2,Inhibitor,GPR109A,MK6892,inhibit,MK 6892;2-[[3-[3-(5-Hydroxy-2-pyridinyl)-1,2,4-oxadiazol-5-yl]-2,2-dimethyl-1-oxopropyl]amino]-1-cyclohexene-1-carboxylic acid;1-Cyclohexene-1-carboxylic acid, 2-[[3-[3-(5-hydroxy-2-pyridinyl)-1,2,4-oxadiazol-5-yl]-2,2-dimethyl-1-oxopropyl]amino]-
- CBNumber
- CB62628149
- Molecular Formula
- C19H22N4O5
- Formula Weight
- 386.4
- MOL File
- 917910-45-3.mol
MK-6892 Property
- storage temp.
- Store at -20°C
- solubility
- ≥34.9 mg/mL in DMSO; ≥3.41 mg/mL in EtOH with ultrasonic; insoluble in H2O
N-Bromosuccinimide Price
- Product number
- CS-1480
- Product name
- MK-6892
- Purity
- 99.43%
- Packaging
- 5mg
- Price
- $300
- Updated
- 2021/12/16
- Product number
- CS-1480
- Product name
- MK-6892
- Purity
- 99.43%
- Packaging
- 10mg
- Price
- $456
- Updated
- 2021/12/16
- Product number
- A3623
- Product name
- MK-6892
- Packaging
- 10mg
- Price
- $557
- Updated
- 2021/12/16
- Product number
- API0014020
- Product name
- MK-6892
- Purity
- 95.00%
- Packaging
- 0.1G
- Price
- $723
- Updated
- 2021/12/16
- Product number
- CS-1480
- Product name
- MK-6892
- Purity
- 99.43%
- Packaging
- 50mg
- Price
- $1080
- Updated
- 2021/12/16
MK-6892 Chemical Properties,Usage,Production
Biological Activity
mk-6892 is a highly potential gpr109a agonists.
in vitro
despite the increased serum shift of these compounds, the representative 1e was highly potent. furthermore, these compounds had no activity on gpr109b and gpr81, the two most closely related gpcrs with 96% and 50% sequence identity to gpr109a,respectively [1].
in vivo
na or mk-6892 was orally administered to wt or na receptor null mice on the same c57bl/6 genetic background. after 15 min of 100 mpk dosing of na or mk-6892 to fed wt or na receptor null mice, the blood levels of mk-6892 at 15 min were 229 μm (950-fold greater than the in vitro ec50 determined in mouse na receptor gtpγs assay, which is 240 nm) in wt mice and 148 μm (620-fold greater than the in vitro ec50) in na receptor null mice [1].
IC 50
ic50 value: 4.0 nm (ki for human gpr109a) [1]