Products for Research Use Only

ADH-503

CAT: 0013-GTR19167407-05Size: 25 mgDry Ice: NoHazardous: No
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CAT#:0013-GTR19167407-05Size:25 mg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
ADH-503 (GB1275) is an orally active, allosteric agonist of CD11b. It reprograms tumor-associated macrophages, reduces immunosuppressive myeloid cell infiltration, and enhances dendritic cell activity. This small molecule is utilized in immuno-oncology research to study macrophage polarization and antitumor immune responses in both cellular and animal models.
CAS Number
2055362-74-6
Product Name Alternative
Complement System, ComplementSystem, CD11b, dendritic, ADH503, ADH-503, ADH 503, allosteric, Inhibitor, GB1275, GB-1275, GB 1275, macrophages, orally, inhibit, immunosuppressive, repolarization, tumorassociated, tumor-infiltrating
Field of Research
Immunology & Inflammation, Metabolism Research, Signal Transduction
Purity
97.03% (May vary between batches)
Solubility
DMSO:5.25 mg/mL (10.01 mM)
Smiles
C[N+] (C) (C) CCO.[O-]C (=O) c1ccc (cc1) -c1ccc (\C=C2/SC (=S) N (Cc3ccccc3) C2=O) o1
Molecular Formula
C27H28N2O5S2
Molecular Weight
524.7
Storage Conditions
-20°C
Notes
For research use only.

Chemical Information

Adh-503

CD11b Agonist GB1275 is an orally bioavailable small molecule agonist of CD11b (integrin alpha-M; ITGAM; integrin alpha M chain), with potential immunomodulating activity. Upon administration, CD11b agonist GB1275 targets and binds to CD11b, thereby activating CD11b. This leads to CD11b-mediated signaling and promotes pro-inflammatory macrophage polarization while suppressing immunosuppressive macrophage polarization. This reduces influx of tumor-associated macrophages (TAMs) and myeloid-derived suppressor cells (MDSCs) in the tumor microenvironment (TME), promotes anti-tumor immune responses, induces cytotoxic T-lymphocytes (CTLs) and suppresses tumor growth. CD11b, a member of the integrin family of cell adhesion receptors highly expressed on immune system cells, is a negative regulator of immune suppression and activates anti-tumor innate immunity.

CAS Number2055362-74-6
PubChem CID145711124
IUPAC Name4-[5-[(Z)-(3-benzyl-4-oxo-2-sulfanylidene-1,3-thiazolidin-5-ylidene)methyl]furan-2-yl]benzoate;2-hydroxyethyl(trimethyl)azanium
Molecular FormulaC27H28N2O5S2
Molecular Weight524.7
Topological Polar Surface Area151
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count7
Rotatable Bond Count6
Heavy Atom Count36
Formal Charge0
Complexity721
SMILES
C[N+](C)(C)CCO.C1=CC=C(C=C1)CN2C(=O)/C(=C/C3=CC=C(O3)C4=CC=C(C=C4)C(=O)[O-])/SC2=S
InChI
InChI=1S/C22H15NO4S2.C5H14NO/c24-20-19(29-22(28)23(20)13-14-4-2-1-3-5-14)12-17-10-11-18(27-17)15-6-8-16(9-7-15)21(25)26;1-6(2,3)4-5-7/h1-12H,13H2,(H,25,26);7H,4-5H2,1-3H3/q;+1/p-1/b19-12-;
InChIKey
GOWDQYRMBCOOJR-JHMJKTBASA-M
Chemical Structure
2D Structure
2D structure of Adh-503
CAS: 2055362-74-6
CID: 145711124
Formula: C27H28N2O5S2
MW: 524.7
Interactive 3D Structure
Loading 3D structure...
Computed Properties
PropertyValue
Molecular Weight524.7
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count7
Rotatable Bond Count6
Exact Mass524.14396435
Monoisotopic Mass524.14396435
Topological Polar Surface Area151 Ų
Heavy Atom Count36
Formal Charge0
Complexity721
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count2
Compound Is CanonicalizedYes