G150
CAS No. 2369751-30-2
G150( —— )
Catalog No. M24083 CAS No. 2369751-30-2
G150 inhibited interferon expression triggered by DSDNA with IC50 of 10.2 nM.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 286 | In Stock |
|
| 5MG | 261 | In Stock |
|
| 10MG | 376 | In Stock |
|
| 25MG | 645 | In Stock |
|
| 50MG | 824 | In Stock |
|
| 100MG | 1070 | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product NameG150
-
NoteResearch use only, not for human use.
-
Brief DescriptionG150 inhibited interferon expression triggered by DSDNA with IC50 of 10.2 nM.
-
DescriptionG150 inhibited interferon expression triggered by DSDNA with IC50 of 10.2 nM.G150 is an effective and highly selective inhibitor of human cyclic GMP-AMP synthase (H-CGAS).
-
In VitroG150 (0.1-100 μM; 1 h) affects IFNB1 and CXCL10 expression in human THP1 cells and primary human macrophages.?G150 (5-10 μM; 1 h) affects dsDNA sensing in THP1 cells and primary human macrophages.?G150 (0.1-100 μM; 1 h) affects the NF-κB pathway activation in THP1-Dual cells.RT-PCR Cell Line:Human THP1 cells and primary human macrophages Concentration:0.1-100 μM Incubation Time:1 hour Result:Dose-dependently inhibited IFNB1 and interferon-stimulated genes monitoring CXCL10 expression with IC50s of 1.96 and 7.57 μM respectively in human THP1 cells, and inhibited IFNB1 and CXCL10 expression with IC50s of 0.62 and 0.87 μM respectively in primary human macrophages.RT-PC RCell Line:Human THP1 cells and primary human macrophages Concentration:5 and 10 μM Incubation Time:1 hour Result:Inhibited dsDNA sensing with a concentration of 10 μM in THP1 cells and with a concentration of 5 μM in primary human macrophages.RT-PCR Cell Line:THP1-Dual cells Concentration:0.1-100 μM Incubation Time:1 hour Result:Inhibited SEAP activity and luciferase activity with IC50s of 0.90 and 1.79 μM respectively in THP1-Dual cells.
-
In Vivo——
-
Synonyms——
-
PathwayCell Cycle/DNA Damage
-
TargetDNA/RNA Synthesis
-
RecptordsDNA/cGAS|h-cGAS
-
Research Area——
-
Indication——
Chemical Information
-
CAS Number2369751-30-2
-
Formula Weight391.25
-
Molecular FormulaC18H16Cl2N4O2
-
Purity>98% (HPLC)
-
SolubilityDMSO:120 mg/mL (306.71 mM; Need ultrasonic)
-
SMILESNc(cc1)ncc1-c(c1c2[nH]c(CC3)c1CN3C(CO)=O)cc(Cl)c2Cl
-
Chemical Name——
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
-
HALOFUGINONE LACTATE
HALOFUGINONE LACTATE is a halogenated derivative of febrifugine, a natural quinazolinone-containing compound found in the Chinese herb D. febrifuga.Halofuginone inhibits prolyl-tRNA synthetase in an ATP-dependent manner with a Ki of 18.3 nM.?Halofuginone is a specific inhibitor of type-I collagen synthesis and attenuates osteoarthritis (OA) by inhibition of TGF-β activityhalofuginone (HF), a widely studied derivative of febrifugine, inhibits the development of T(H)17-driven autoimmunity in a mouse model of multiple sclerosis by activating the amino acid response (AAR) pathway.?HF binds glutamyl-prolyl-tRNA synthetase (EPRS), inhibiting prolyl-tRNA synthetase activity;?this inhibition is reversed by the addition of exogenous proline or EPRS.
-
Asiaticoside
Asiaticoside (Madecassol) is the active chemical component of the plant Centella asiatica. Asiaticoside is used to study potential treatments for wounds and burns.
-
RP-6685
RP-6685, a highly potent and selective inhibitor of DNA polymerase theta (Polθ), manifests remarkable oral activity.
Cart
sales@molnova.com