cas 1857296-22-0|| where to buy 5-formyl-4-methyl-1H-indole-2-carbonitrile

Product Name:5-formyl-4-methyl-1H-indole-2-carbonitrile

IUPAC Name:5-formyl-4-methyl-1H-indole-2-carbonitrile

Packing Unit	Available Stock	Price($)
CM327321-5g	in stock	Ǒƴȅ
CM327321-25g	in stock	ȅƚŞŞ

For R&D use only.

Inquiry Form

Chemical Name

CAS Number

Quantity*

Required Specifications*
(Assay %, Material Grade etc.)

Contact Name*

Contact Email*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 1857296-22-0 regularly via the above email.

Additional Notes

Verification code*

refresh

: CAS NO:1857296-22-0; Molecular Formula:C11H8N2O; Melting Point:-; Smiles Code:N#CC(N1)=CC2=C1C=CC(C=O)=C2C; Density:

: Catalog Number:CM327321; Molecular Weight:184.2; Boiling Point:; MDL No:; Storage:

: Indoles; Indole is a compound of pyrrole and benzene in parallel, also known as benzopyrrole. There are two combinations of pyrrole and benzene, called indole and isoindole, respectively. Many derivatives of indole have physiological and pharmacological activities, and can synthesize vasodilators, antihistamines, antipyretic analgesics, etc. in medicine, so indole is also a very important heterocyclic compound.; indole company; As a indole company,we sincerely welcome the new and old friends from home and abroad to synergize with our company and share the benefits and opportunities.

: Ziftomenib; Kura Oncology reported preliminary clinical data from the first 20 patients in KOMET-007, a Phase 1 dose-escalation trial of the Company's potent and selective menin inhibitor, ziftomenib, in combination with standards of care, including cytarabine/daunorubicin (7+3) and venetoclax/azacitidine (ven/aza), in patients with NPM1-mutant (NPM1-m) and KMT2A-rearranged (KMT2A-r) acute myeloid leukemia (AML). Ziftomenib is a novel, once-daily, oral investigational drug candidate targeting the menin-KMT2A/MLL protein-protein interaction for treatment of genetically defined AML patients with high unmet need. In preclinical models, ziftomenib inhibits the KMT2A/MLL protein complex and exhibits downstream effects on HOXA9/MEIS1 expression and potent anti-leukemic activity in genetically defined preclinical models of AML. Ziftomenib has received Orphan Drug Designation from the FDA for the treatment of AML.
Chemenu has been working to develop more compounds for drug discovery. Here are the building blocks we can provide.