Products for Research Use Only
RegisterLogin

HC-7366

CAT: 0013-GTR19235333-04Size: 10 mgDry Ice: NoHazardous: No
Product image 1
1 / 1
CAT#:0013-GTR19235333-04Size:10 mg
Selected
24/48H Stock Items & 2 to 6 Weeks non Stock Items.
Quick Request Actions
Description
HC-7366 (GCN2 modulator-1) is an orally bioavailable, small-molecule activator of GCN2 kinase. It demonstrates antitumor activity by inducing integrated stress response pathways, leading to tumor growth inhibition in preclinical in vivo models, making it a valuable research tool for oncology and immunometabolism studies.
CAS Number
2803470-63-3
Product Name Alternative
GCN2 modulator-1, HC7366
Field of Research
Cell Biology
Purity
99.84% (May vary between batches)
Solubility
DMSO:20 mg/mL (39.3 mM)
Smiles
O=C (NC) C=1N=CN2C=C (N=CC12) C3=C (F) C=CC (NS (=O) (=O) C4=CC (Cl) =CN=C4OC) =C3F
Molecular Formula
C20H15ClF2N6O4S
Molecular Weight
508.89
Storage Conditions
-20°C
Notes
For research use only.

Chemical Information

Hibercell GCN2 inhibitor HC-7366

GCN2 Activator HC-7366 is an activator of the serine/threonine protein kinase general control nonderepressible 2 (GCN2), with potential antineoplastic and immunomodulating activities. Upon administration, GCN2 activator HC-7366 targets and binds to, and activates GCN2, which phosphorylates eukaryotic translation initiation factor 2A (eIF2A), thereby inducing cyclic AMP-dependent transcription factor ATF-4 transcription and ATF-4-mediated integrated stress response (ISR). This may result in apoptosis. GCN2 plays a key role in the activation of the ISR pathway in response to amino acid deprivation and in hypoxic tumors. While ISR promotes the adaptation of tumor cells to hypoxic stress, prolonged activation of ISR induces apoptosis.

CAS Number2803470-63-3
PubChem CID164593978
IUPAC Name6-[3-[(5-chloro-2-methoxy-3-pyridinyl)sulfonylamino]-2,6-difluorophenyl]-N-methylimidazo[1,5-a]pyrazine-1-carboxamide
Molecular FormulaC20H15ClF2N6O4S
Molecular Weight508.9
XLogP2.6
Topological Polar Surface Area136
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count10
Rotatable Bond Count6
Heavy Atom Count34
Formal Charge0
Complexity838
SMILES
CNC(=O)C1=C2C=NC(=CN2C=N1)C3=C(C=CC(=C3F)NS(=O)(=O)C4=C(N=CC(=C4)Cl)OC)F
InChI
InChI=1S/C20H15ClF2N6O4S/c1-24-19(30)18-14-7-25-13(8-29(14)9-27-18)16-11(22)3-4-12(17(16)23)28-34(31,32)15-5-10(21)6-26-20(15)33-2/h3-9,28H,1-2H3,(H,24,30)
InChIKey
KIGXQRBUVDDSPP-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of Hibercell GCN2 inhibitor HC-7366
CAS: 2803470-63-3
CID: 164593978
Formula: C20H15ClF2N6O4S
MW: 508.9
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight508.9
XLogP32.6
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count10
Rotatable Bond Count6
Exact Mass508.0532082
Monoisotopic Mass508.0532082
Topological Polar Surface Area136 Ų
Heavy Atom Count34
Formal Charge0
Complexity838
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count1
Compound Is CanonicalizedYes

Related Products

CatalogName
GTR19159292-01HC-067047
GTR19174462-01HC-070
GTR19028269Hc-CATH
GTR19197543-01HC-3
GTR19159602-01HC-030031
GTR19208178-01Apatinib HC
GTR19191854-01HC Toxin
GTR19062961-01Hc-CATH
GTR19235287-01HC-5404
GTR19169841-01HC-030031

Alternative Products

CatalogName
E1975-01HC-7366
TL308496UGT2B15 Human shRNA Plasmid Kit (Locus ID 7366)
SR305030UGT2B15 Human siRNA Oligo Duplex (Locus ID 7366)
B7588-50HC 067047
531948HC-056456
HY-157231HC-5404
HY-P10431Hc-CATH
HY-157306HC-1310
MBS6109373-01HC 030031
E1884-5mgHC-258

Popular Products