ChemicalBook > CAS DataBase List > Loxoribine

Loxoribine

Product Name
Loxoribine
CAS No.
121288-39-9
Chemical Name
Loxoribine
Synonyms
RWJ 21757;Loxoribine;7,8-Dihydro-8-oxo-7-allyl-guanosine;7-Allyl-7,8-dihydro-8-oxoguanosine 95%;7-ALLYL-7 8-DIHYDRO-8-OXOGUANOSINE 95;7,8-Dihydro-8-oxo-7-(2-propenyl)guanosine;Guanosine, 7,8-dihydro-8-oxo-7-(2-propenyl)-;7,8-dihydro-8-oxo-7-allyl-guanosine, Loxoribine;Guanosine, 7,8-dihydro-8-oxo-7-(2-propen-1-yl)-;7-Allyl-7,8-dihydro-8-oxoguanosine (Loxoribine)
CBNumber
CB7499469
Molecular Formula
C13H17N5O6
Formula Weight
339.3
MOL File
121288-39-9.mol
More
Less

Loxoribine Property

Melting point:
227-230 °C(lit.)
Density 
1.92±0.1 g/cm3(Predicted)
storage temp. 
Desiccate at +4°C
solubility 
Soluble in DMSO (up to 25 mg/ml).
form 
White to off-white solid.
pka
10.29±0.20(Predicted)
color 
White
optical activity
[α]21/D 32°, c = 1 in H2O
Stability:
Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
More
Less

Safety

WGK Germany 
3
HS Code 
29349990
More
Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

More
Less

N-Bromosuccinimide Price

Sigma-Aldrich
Product number
496812
Product name
7-Allyl-7,8-dihydro-8-oxoguanosine
Purity
95%
Packaging
50mg
Price
$82.4
Updated
2024/03/01
Sigma-Aldrich
Product number
496812
Product name
7-Allyl-7,8-dihydro-8-oxoguanosine
Purity
95%
Packaging
250mg
Price
$192.4
Updated
2024/03/01
Cayman Chemical
Product number
21186
Product name
Loxoribine
Purity
≥98%
Packaging
5mg
Price
$32
Updated
2024/03/01
Cayman Chemical
Product number
21186
Product name
Loxoribine
Purity
≥98%
Packaging
10mg
Price
$61
Updated
2024/03/01
Cayman Chemical
Product number
21186
Product name
Loxoribine
Purity
≥98%
Packaging
25mg
Price
$86
Updated
2024/03/01
More
Less

Loxoribine Chemical Properties,Usage,Production

Description

Loxoribine is a guanosine derivative and an agonist of toll-like receptor 7 (TLR7). It is selective for TLR7 over other human TLRs in a cell-based reporter assay at 1 mM.. Loxoribine induces proliferation, increases the antibody response to sheep red blood cells, and activates natural killer cell activity against Yac-1 lymphoma cells in murine splenocyte cultures (EC50s = 10-50, 3-20, and 13-22 μM, respectively). Loxoribine (250 μM) increases production of IL-12, IL-23, IL-27, and IL-10 by human monocyte-derived dendritic cells (MoDCs). Loxoribine-treated MoDCs induce higher levels of IL-17 and IFN-γ secretion by co-cultured allogeneic CD4+ T cells compared to control MoDCs. Loxoribine (120 mg/kg) reduces the number of pulmonary metastases in the B16 mouse model of melanoma, an effect enhanced by co-administration of IL-2, and exhibits adjuvant activity in mice immunized with a B16 tumor vaccine.

Chemical Properties

White Solid

Uses

7-Allyl-7,8-dihydro-8-oxoguanosine (Loxoribine) is a small-molecule immunostimulant. Loxoribine is a toll-like receptor 7 (TLR7) agonist; induces immune cell activation and increases cytokine product ion. Loxoribine displays antitumor and antiviral activity in various animal models.

Uses

Loxoribine is a selective toll-like receptor 7 (TLR7) agonist that activates immune cells and increases cytokine production.

Uses

Small-molecule immunostimulants

Biological Activity

Toll-like receptor 7 (TLR7) agonist; induces immune cell activation and increases cytokine production. Displays antitumor and antiviral activity in various animal models.

References

1) Heil?et al.?(2003),?The Tool-like receptor 7 (TLR7)-specific stimulus loxoribine uncovers a strong relationship within the TLR7, 8 and 9 subfamily; Eur. J. Immunol.,?33?2987 2) Goodman?et al.?(1995),?A new approach to vaccine adjuvants. Immunopotentiation by intracellular T-helper-like signals transmitted by loxoribine;?Pharm. Biotechnol.,?6?581 3) Girart?et al.?(2007), Engagement of TLR3, TLR7 and NKG2D regulate IFN-gamma secretion but not NKG2D-mediated cytotoxicity by human NK cells stimulated with suboptimal doses of IL-12; J. Immunol.,?179?3472 4) Stewart?et al.?(2012),?Toll-like receptor 7 ligands inhibit influenza A infection in chickens; J. Interferon Cytokine Res,,?32?46 5) Wang?et al.?(2015),?The TLR7 agonist induces tumor regression both by promoting CD4-T cells proliferation and by reversing T regulatory cell-mediated suppression via dendritic cells; Oncotarget,?6?1779

Loxoribine Preparation Products And Raw materials

Raw materials

Preparation Products

More
Less

Loxoribine Suppliers

EMMX Biotechnology LLC
Tel
888-539-0666
Fax
888-539-0666
Email
info@emmx.com
Country
United States
ProdList
8449
Advantage
60
BOC Sciences
Tel
+16314854226
Email
inquiry@bocsci.com
Country
United States
ProdList
19743
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
19892
Advantage
58
BOC Sciences
Tel
16314854226
Email
info@bocsci.com
Country
United States
ProdList
9926
Advantage
65

121288-39-9, LoxoribineRelated Search:


  • 7-ALLYL-7 8-DIHYDRO-8-OXOGUANOSINE 95
  • Loxoribine
  • 7-Allyl-2-amino-9-(3,4-dihydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-7,9-dihydro-1H-purine-6,8-dione
  • 7,8-Dihydro-8-oxo-7-(2-propenyl)guanosine
  • RWJ 21757
  • Guanosine, 7,8-dihydro-8-oxo-7-(2-propenyl)-
  • 7-Allyl-7,8-dihydro-8-oxoguanosine 95%
  • 7,8-Dihydro-8-oxo-7-allyl-guanosine
  • 7-Allyl-7,8-dihydro-8-oxoguanosine (Loxoribine)
  • Guanosine, 7,8-dihydro-8-oxo-7-(2-propen-1-yl)-
  • 7,8-dihydro-8-oxo-7-allyl-guanosine, Loxoribine
  • 7-ALLYL-7 8-DIHYDRO-8-OXOGUANOSINE 95 USP/EP/BP
  • RWJ-21757,Loxoribine,natural,Toll-like Receptor (TLR),killer,cells,Influenza Virus,Inhibitor,cells,inhibit,TLR-7,MoDCs,RWJ21757
  • 121288-39-9
  • Heterocyclic Compounds
  • Bases & Related Reagents
  • Heterocycles
  • Nucleotides
  • Nucleosides
  • Oligonucleotide Synthesis
  • Specialty Synthesis