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Talarozole

Cat. No. M14529

All AbMole products are for research use only, cannot be used for human consumption.

Talarozole Structure
Synonym:

R115866

Size Price Availability Quantity
10mM*1mL in DMSO USD 118 In stock
1mg USD 68 In stock
2mg USD 106 In stock
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Quality Control & Documentation
Biological Activity

Talarozole (R115866) is an oral systemic all-trans retinoic acid metabolism blocking agent (RAMBA) which increases intracellular levels of endogenous all-trans retinoic acid (RA). Talarozole inhibits both CYP26A1 and CYP26B1 with IC50s of 5.4 and 0.46 nM, respectively.

Chemical Information
Molecular Weight 377.51
CAS Number 201410-53-9
Solubility (25°C) DMSO ≥ 36 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Ni Yang, et al. Cardiac retinoic acid levels decline in heart failure

[2] Joachim G S Veit, et al. Characterization of CYP26B1-Selective Inhibitor, DX314, as a Potential Therapeutic for Keratinization Disorders

[3] B Baert, et al. Local skin pharmacokinetics of talarozole, a new retinoic acid metabolism-blocking agent

[4] E Pavez Lori, et al. Topical treatment with CYP26 inhibitor talarozole (R115866) dose dependently alters the expression of retinoid-regulated genes in normal human epidermis

[5] Aanand N Geria, et al. Talarozole, a selective inhibitor of P450-mediated all-trans retinoic acid for the treatment of psoriasis and acne

Related RAR/RXR Products
Acitretin (Ro 10-1670)

Acitretin (Ro 10-1670) is a second-generation retinoid.

Adapalene

Adapalene is a third-generation topical retinoid, it is a potent RAR agonist, with AC50 values of 2.3 nM, 9.3 nM, and 22 nM for RARβ, RARγ, RARα, respectively. Adapalene also inhibits the enzymatic activity of GOT1 in a non-competitive manner. Adapalene is also an MST1 agonist.

Tamibarotene

Tamibarotene is a synthetic retinoic acid receptor (RAR) agonist with high specificity for RARα and RARβ over RARγ.

TTNPB

TTNPB (Arotinoid Acid) is a potent RAR agonist, and inhibits binding of [3H]tRA with IC50 of 5.1 nM, 4.5 nM, and 9.3 nM for human RARα, β, and γ, respectively.

Fenretinide

Fenretinide (4-HPR) is a synthetic retinoid deriverative. Fenretinide is shown to exhibit binding to the retinoic acid receptors (RAR) at concentrations necessary to induce cell death.

  Catalog
Abmole Inhibitor Catalog




Keywords: Talarozole, R115866 supplier, RAR/RXR, inhibitors, activators

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