Structure

InChI Key WJEOLQLKVOPQFV-UHFFFAOYSA-N
Smile Cc1ccc(NC(=O)c2ccc(CN3CCN(C)CC3)cc2)cc1Nc1nc(-c2cccnc2)cs1
InChI
InChI=1S/C28H30N6OS/c1-20-5-10-24(16-25(20)31-28-32-26(19-36-28)23-4-3-11-29-17-23)30-27(35)22-8-6-21(7-9-22)18-34-14-12-33(2)13-15-34/h3-11,16-17,19H,12-15,18H2,1-2H3,(H,30,35)(H,31,32)

Physicochemical Descriptors

Property Name Value
Molecular Formula C28H30N6OS
Molecular Weight 498.66
AlogP 5.26
Hydrogen Bond Acceptor 7.0
Hydrogen Bond Donor 2.0
Number of Rotational Bond 7.0
Polar Surface Area 73.39
Molecular species NEUTRAL
Aromatic Rings 4.0
Heavy Atoms 36.0

Pharmacology

Action Mechanism of Action Reference
INHIBITOR Fibroblast growth factor receptor 3 inhibitor PubMed PubMed Other
Primary Target
KIT proto-oncogene, receptor tyrosine kinase

Indications

Mesh Heading Maximum Phase Mesh ID Reference
Neoplasms 3 D009369 ClinicalTrials
Multiple Myeloma 3 D009101 ClinicalTrials
Melanoma 3 D008545 ClinicalTrials
Pancreatic Neoplasms 3 D010190 ClinicalTrials
Amyotrophic Lateral Sclerosis 3 D000690 ClinicalTrials
Prostatic Neoplasms, Castration-Resistant 3 D064129 ClinicalTrials
Mastocytosis, Systemic 3 D034721 ClinicalTrials
Multiple Sclerosis, Chronic Progressive 3 D020528 ClinicalTrials
Alzheimer Disease 3 D000544 ClinicalTrials
Asthma 3 D001249 ClinicalTrials
Gastrointestinal Stromal Tumors 3 D046152 ClinicalTrials
Multiple Sclerosis 2 D009103 ClinicalTrials
Arthritis, Rheumatoid 2 D001172 ClinicalTrials
Severe Acute Respiratory Syndrome 2 D045169 ClinicalTrials
Mastocytosis 2 D008415 ClinicalTrials
Psoriasis 2 D011565 ClinicalTrials
Ovarian Neoplasms 2 D010051 ClinicalTrials

Related Entries

MCS

Scaffolds

Cross References

Resources Reference
CAS NUMBER 790299-79-5
ChEBI 63450
ChEMBL CHEMBL1908391
DrugBank DB11526
FDA SRS M59NC4E26P
Guide to Pharmacology 5656
PDB G65
PubChem 10074640
SureChEMBL SCHEMBL717239
ZINC ZINC000034177219