CasNo.608141-41-9,Apremilast,(608141-41-9) Suppliers

100 Gram	Negotiable

Min.Order :100 Gram
Purity: 99%
Payment Terms : T/T,Other

Keywords

Apremilast 608141-41-9 99%purity

Quick Details

Appearance:White to Pale Yellow powder
Application:API
PackAge:according to the need of packing
ProductionCapacity:100|Kilogram|Day
Storage:2-8°C
Transportation:SEA/COURIER/AIR

Superiority:

Product Name:   Apremilast
Synonyms:   (S)-N-(2-(1-(3-Ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl)-1,3-dioxoisoindolin-4-yl)acetamide;ApreMilast,CC-10004;brand name: Otezla.;CC10004; CC-10004; CC 10004; APREMILAST; BRAND NAME: OTEZLA.;(S)-4-Acetylamino-2-[1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl]isoindoline-1,3-dione;Apster;CS-1055;CC 10004; CC10004; CC-10004
CAS:   608141-41-9
MF:   C22H24N2O7S
MW:   460.5
EINECS:   807-237-6
Product Categories:   Other series;Inhibitors;Inhibitor;GS;API
Mol File:   608141-41-9.mol

Apremilast Chemical Properties
Melting point    152-156°C
Boiling point    741.3±60.0 °C(Predicted)
density    1.381
storage temp.    Refrigerator
solubility    Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly, Heated)
pka   14.01±0.20(Predicted)
form    Solid
color    White to Pale Yellow
InChIKey   IMOZEMNVLZVGJZ-QGZVFWFLSA-N
SMILES   C(NC1=CC=CC2=C1C(=O)N([C@@H](C1=CC=C(OC)C(OCC)=C1)CS(C)(=O)=O)C2=O)(=O)C
CAS DataBase Reference   608141-41-9

Details:

Apremilast Usage And Synthesis
Description   Apremilast (Otezla) was approved by the FDA on March 21, 2014 for the treatment of adult patients with active psoriatic arthritis. Apremilast is a member of a new class of oral small molecule inhibitors of the phosphosphodiesterase 4 (PDE4) enzyme. When PDE4 is inhibited in immune cells, it results in elevation of intracellular cyclic adenosine monophosphate (cAMP) levels, which can regulate inflammatory mediators. The current clinical data indicate that apremilast is an effective and well tolerated option for the management of psoriasis and PsA in adults.
Uses   Treating active psoriatic arthritis. It is also used to treat moderate to severe plaque psoriasis in certain patients.
Metabolism and Drug interaction   Oral administration of apremilast has an absolute biovailability of 73% with peak concentration at 2.5 hours (Tmax). The half-life of apremilast is 6-9 hours. Apremilast is metabolized by the both cytochrome (CYP) and non-CYP pathways. In vitro studies have demonstrated that apremilast metabolism is primarily mediated by the CYP3A4 pathway. Thus, concomitant use of apremilast with CYP450 enzyme inducers (such as rifampin, phenobarbital, carbamazepine, phenytoin) is not recommended. There are no significant drug-drug interactions with oral contraceptives, ketoconazole, or methotrexate.
safety information   1.Apremilast may cause depression. The risk may be greater in patients who have a history of depression or suicidal thoughts or actions. Families and caregivers must closely watch patients who take apremilast. It is important to keep in close contact with the patient's doctor. Tell the doctor right away if the patient has new, worsened, or sudden symptoms, such as depression; anxiety, restlessness, or irritability; panic attacks; or any changes in behavior. Contact the doctor right away if any signs of suicidal thoughts or actions occur.
2.Apremilast may cause weight loss. You will need to have regular weight checks while you are taking apremilast.