Lotamilast

Additional information:
Lotamilast (RVT-501; E6005) is a selective phosphodiesterase 4 (PDE4) inhibitor with an IC50 of 2.8 nM.|Product information|CAS Number: 947620-48-6|Molecular Weight: 472.49|Formula: C26H24N4O5|Chemical Name: methyl 4-(3-[6,7-dimethoxy-2-(methylamino)quinazolin-4-yl]phenylcarbamoyl)benzoate|Smiles: CNC1=NC2=CC(OC)=C(C=C2C(=N1)C1=CC(=CC=C1)NC(=O)C1C=CC(=CC=1)C(=O)OC)OC|InChiKey: BBTFKAOFCSOZMB-UHFFFAOYSA-N|InChi: InChI=1S/C26H24N4O5/c1-27-26-29-20-14-22(34-3)21(33-2)13-19(20)23(30-26)17-6-5-7-18(12-17)28-24(31)15-8-10-16(11-9-15)25(32)35-4/h5-14H,1-4H3,(H,28,31)(H,27,29,30)|Technical Data|Appearance: Solid Power|Purity: ≥98% (or refer to the Certificate of Analysis)|Solubility: DMSO : 25 mg/mL (52.91 mM; Need ultrasonic).|Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis|Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.|Shelf Life: ≥12 months if stored properly.|Stock Solution Storage: 0 – 4 oC for 1 month or refer to the Certificate of Analysis.|Drug Formulation: To be determined|HS Tariff Code: 382200|How to use|In Vitro:|Lotamilast potently and selectively inhibits human PDE4 activity with an IC50 of 2.M‑89 Technical Information 8 nM and suppresses the production of various cytokines from human lymphocytes and monocytes with IC50 values ranging from 0.Fluralaner site 49 to 3.PMID:33222099 1 nM.|In Vivo:|Lotamilast is currently in phase 2 development for patients with mild-to-moderate atopic dermatitis. In mice models, the topical application of Lotamilast produces an immediate antipruritic effect as well as an anti-inflammatory effect with reduced expression of cytokines/adhesion molecules. On the basis of these observed effects, topical RVT-501 ameliorates the appearance of atopic dermatitis-like skin lesions in two types of AD models, hapten- and mite-elicited models, exhibiting inhibitory effects comparable to that of tacrolimus. A single topical application of Lotamilast significantly inhibits spontaneous scratching during 1–2 h after application in mice with chronic dermatitis; the inhibition is partial and similar between 0.01% and 0.03%. Topical application of 0.03% Lotamilast to the rostral back significantly inhibits the increased activity of the cutaneous nerve in mice with chronic dermatitis. The cutaneous concentration of cAMP is significantly decreased in mice with chronic dermatitis, and this decrease is reversed by topical Lotamilast application.|Products are for research use only. Not for human use.|