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INDEX NAME NOT YET ASSIGNED

CAS No.
2712126-48-0
Chemical Name:
INDEX NAME NOT YET ASSIGNED
Synonyms
1-(2-(methyl-d3)propyl-1,1,2,3,3,3-d6)-1H-imidazo[4,5-c]quinolin-4-amine
CBNumber:
CB212806832
Molecular Formula:
C14H16N4
Molecular Weight:
240.31
MDL Number:
MOL File:
2712126-48-0.mol
Last updated:2023-06-08 09:03:09

INDEX NAME NOT YET ASSIGNED Properties

solubility DMF: 1 mg/ml; DMSO: 1 mg/ml
form A solid

SAFETY

Risk and Safety Statements

INDEX NAME NOT YET ASSIGNED price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Cayman Chemical 26424 Imiquimod-d9 ≥99% deuterated forms (d1-d9) 2712126-48-0 500 μg $242 2024-03-01 Buy
Cayman Chemical 26424 Imiquimod-d9 ≥99% deuterated forms (d1-d9) 2712126-48-0 1 mg $459 2024-03-01 Buy
Product number Packaging Price Buy
26424 500 μg $242 Buy
26424 1 mg $459 Buy

INDEX NAME NOT YET ASSIGNED Chemical Properties,Uses,Production

Description

Imiquimod-d9 is intended for use as an internal standard for the quantification of imiquimod by GC- or LC-MS. Imiquimod is an imidazoquinoline agonist of toll-like receptor 7 (TLR7; EC50 = 2.12 μM).1 It increases TNF-α and IL-12 p40 production in IFN-γ-treated murine peritoneal macrophages in a concentration- and MyD88-dependent manner.2 Topical application of imiquimod (30 μl of 5% cream) increases TNF and IFN levels at the application site in hairless mice.3 Imiquimod dose-dependently increases serum levels of IFN-α in mice when administered by gavage.4 It reduces tumor growth in an MC-26 model of murine colon cancer when administered at a dose of 30 mg/kg every three days. Imiquimod (5 mg/kg, intravaginally, twice daily) reduces vaginal viral titer and lesion formation in a guinea pig model of genital HSV-2 infection.5 Formulations containing imiquimod have been used in the treatment of actinic keratosis, superficial basal cell carcinoma, and external genital warts.

References

1. Shukla, N.M., Mallardi, S.S., Mutz, C.A., et al. Structure-activity relationships in human toll-like receptor 7-active imidazoquinoline analogues J. Med. Chem. 53(11),4450-4465(2010).
2. Hemmi, H., Kaisho, T., Takeuchi, O., et al. Small anti-viral compounds activate immune cells via the TLR7 MyD88-dependent signaling pathway Nat. Immunol. 3(2),196-200(2002).
3. Imbertson, L.M., Beaurline, J.M., Couture, A.M., et al. Cytokine induction in hairless mouse and rat skin after topical application of the immune response modifiers imiquimod and S-28463 J. Invest. Dermatol. 110(5),734-739(1998).
4. Sidky, Y.A., Borden, E.C., Weeks, C.E., et al. Inhibition of murine tumor growth by an interferon-inducing imidazoquinolinamine Cancer Res. 52(13),3528-3533(1992).
5. Harrison, C.J., Jenski, L.J., Voychehovski, T., et al. Modification of immunological responses and clinical disease during topical R-837 treatment of genital HSV-2 infection Antiviral Res. 10(4-5),209-223(1988).

INDEX NAME NOT YET ASSIGNED Preparation Products And Raw materials

Raw materials

Preparation Products

INDEX NAME NOT YET ASSIGNED Suppliers

Global( 2)Suppliers
Supplier Tel Email Country ProdList Advantage
Shanghai Yifei Biotechnology Co. , Ltd. 021-65675885 18964387627 customer_service@efebio.com China 11974 58
1-(2-(methyl-d3)propyl-1,1,2,3,3,3-d6)-1H-imidazo[4,5-c]quinolin-4-amine 2712126-48-0