1H-Indole-6-carboxamide, 1-[(2-chloro-6-fluorophenyl)methyl]-2,3-dihydro-3,3-dimethyl-2-oxo-N-[(2,4,6-trifluorophenyl)methyl]-
- Product Name
- 1H-Indole-6-carboxamide, 1-[(2-chloro-6-fluorophenyl)methyl]-2,3-dihydro-3,3-dimethyl-2-oxo-N-[(2,4,6-trifluorophenyl)methyl]-
- CAS No.
- 2259624-71-8
- Chemical Name
- 1H-Indole-6-carboxamide, 1-[(2-chloro-6-fluorophenyl)methyl]-2,3-dihydro-3,3-dimethyl-2-oxo-N-[(2,4,6-trifluorophenyl)methyl]-
- Synonyms
- C53;LZAP;MST016;PP1553;OK/SW-cl.114;STING agonist C53;STING activator Compound 53;STING activator Compound 53, 10 mM in DMSO;Recombinant Human CDK5RAP3 protein (His Tag);1-(2-chloro-6-fluorobenzyl)-3,3-dimethyl-2-oxo-N-(2,4,6-trifluorobenzyl)indoline-6-carboxamide
- CBNumber
- CB010785689
- Molecular Formula
- C25H19ClF4N2O2
- Formula Weight
- 490.88
- MOL File
- 2259624-71-8.mol
1H-Indole-6-carboxamide, 1-[(2-chloro-6-fluorophenyl)methyl]-2,3-dihydro-3,3-dimethyl-2-oxo-N-[(2,4,6-trifluorophenyl)methyl]- Property
- Boiling point:
- 628.4±55.0 °C(Predicted)
- Density
- 1.392±0.06 g/cm3(Predicted)
- storage temp.
- 4°C, protect from light
- solubility
- DMSO : 250 mg/mL (509.29 mM; Need ultrasonic)
- form
- A crystalline solid
- pka
- 13.31±0.40(Predicted)
- color
- Light yellow to yellow
- SMILES
- O=C(C1=CC=C2C(N(CC3=C(Cl)C=CC=C3F)C(C2(C)C)=O)=C1)NCC4=C(F)C=C(F)C=C4F
N-Bromosuccinimide Price
- Product number
- SML4208
- Product name
- STING agonist C53
- Purity
- ≥98% (HPLC)
- Packaging
- 1 unit
- Price
- $79
- Updated
- 2025/07/31
1H-Indole-6-carboxamide, 1-[(2-chloro-6-fluorophenyl)methyl]-2,3-dihydro-3,3-dimethyl-2-oxo-N-[(2,4,6-trifluorophenyl)methyl]- Chemical Properties,Usage,Production
Uses
STING agonist-12 (Compound 53) is a potent, orally active human STING activator with an EC50 of 185 nM[1].
Biological Activity
STING agonist-12 (Compound 53) is a potent, orally active human STING activator with an EC50 of 185 nM[1]. STING agonist-12 (Compound 53) (10 μM) shows excellent pan-polymorph activity across the panel of STING proteins (92%, 107% and 92% against R232, H232 and HAQ, respectively) in HEK293T cells[1].STING agonist-12 is not active at mouse STING[1]. STING agonist-12 (Compound 53) (5 mpk for i.v.; 10 mpk for p.o.) is well-absorbed with a short terminal half-life[1].
in vivo
STING agonist-12 (Compound 53) (5 mpk for i.v.; 10 mpk for p.o.) is well-absorbed with a short terminal half-life[1].
| Animal Model: | Balb/c mice (n=3)[1] | |||||||||||||||||||||
| Dosage: | 5 or 10 mpk | |||||||||||||||||||||
| Administration: | Lateral tail vein or oral gavage (Pharmacokinetic Analysis) | |||||||||||||||||||||
| Result: | Pharmacokinetic profile of STING agonist-12 (Compound 53) in mouse[1].
|
storage
Store at -20°C
References
[1]. Pryde DC, et al. The discovery of potent small molecule activators of human STING. Eur J Med Chem. 2021 Jan 1;209:112869.
1H-Indole-6-carboxamide, 1-[(2-chloro-6-fluorophenyl)methyl]-2,3-dihydro-3,3-dimethyl-2-oxo-N-[(2,4,6-trifluorophenyl)methyl]- Preparation Products And Raw materials
Raw materials
Preparation Products
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