Nom du produit:3,5-dichloropyrazine-2-carbonitrile
IUPAC Name:3,5-dichloropyrazine-2-carbonitrile
- CAS:313339-92-3
- Formule moléculaire:C5HCl2N3
- Pureté:95%+
- Numéro de catalogue:CM102418
- Poids moléculaire:173.98
Pour une utilisation en R&D uniquement..
Détails du produit
- N° CAS:313339-92-3
- Formule moléculaire:C5HCl2N3
- Point de fusion:-
- Code SMILES:ClC1=CN=C(C#N)C(Cl)=N1
- Densité:
- Numéro de catalogue:CM102418
- Poids moléculaire:173.98
- Point d'ébullition:276.6°C at 760 mmHg
- N° Mdl:MFCD13193460
- Stockage:Keep in Inert atmosphere, store at 2-8°C.
Category Infos
- Pyrazines
- Pyrazine is a heterocyclic aromatic organic compound with chemical formula C4H4N2. The marketed pyrazine drugs are mainly distributed in the field of anti-tumor and anti-infection. In recent years, there have been many new drugs in various fields, and there are some new target drugs worthy of attention.
- pyrazine,pyrazine price
- if you want to know the latest news about pyrazine and pyrazine price, please come to our website and get a quote for free.
Column Infos
- NX-2127
- Existing BTK inhibitors directly bind to the active site of BTK and face challenges such as acquired resistance or incomplete responses over time. PROTAC-induced BTK degradation works as a novel alternative therapy for drug-resistant cancers. The latest journal Science publishes the identification of BTK mutations that are susceptible to clinical-stage BTK and IKZF1/3 degrader NX-2127.
Nurix Therapeutics’ TPD compound NX-2127 is a first-in-class, dual-function small-molecule protein degrader. It drives targeted BTK and transcription factor IKAROS (IKZF1/3) degradation through ubiquitination and proteasomal degradation, adding combined benefit. NX-2127 is under development of phase I clinical trials that shows promising results and a manageable safety profile for the treatment of relapsed/ refractory B-cell malignancies.
- NX-5948
- Nurix announced the presentation of the first findings of clinical responses in the brain for NX-5948. NX-5948 is an investigational, orally bioavailable, brain penetrant, small molecule degrader of BTK. NX-5948 is currently being evaluated in a Phase 1 clinical trial in patients with relapsed or refractory B cell malignancies.