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URMC-099 - 96%, high purity , CAS No.1229582-33-5, Inhibitor of cyclin dependent kinase like 2;Inhibitor of death associated protein kinase 3;Inhibitor of fms related receptor tyrosine kinase 3;Inhibitor of leucine rich repeat kinase 2;Inhibitor of mitogen-activated protein kinase kinase kinase 10;Inhibit

Specifications & Purity:  96%
Item Number
U275952
Grouped product items
SKUSizeAvailabilityPrice Qty
U275952-5mg
5mg
In stock
$64.90
U275952-10mg
10mg
In stock
$97.90
U275952-25mg
25mg
In stock
$220.90
U275952-50mg
50mg
In stock
$293.90
U275952-100mg
100mg
In stock
$489.90

Novel bioavailable, brain penetrant MLK inhibitor

Basic Description

Synonyms3-(1H-Indol-5-yl)-5-[4-[(4-methyl-1-piperazinyl)methyl]phenyl]-1Hpyrrolo[2,3-b]pyridine
Specifications & Purity96%
Storage TempStore at -20°C,Argon charged
Shipped InDry ice
Action TypeINHIBITOR
Mechanism of actionInhibitor of cyclin dependent kinase like 2;Inhibitor of death associated protein kinase 3;Inhibitor of fms related receptor tyrosine kinase 3;Inhibitor of leucine rich repeat kinase 2;Inhibitor of mitogen-activated protein kinase kinase kinase 10;Inhibit

Associated Targets

CDKL2 Tchem Cyclin-dependent kinase-like 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DLK1 Tchem Protein delta homolog 1 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DAPK3 Tchem Death-associated protein kinase 3 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SRPK2 Tchem SRSF protein kinase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

FLT3 Tclin Receptor-type tyrosine-protein kinase FLT3 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TNIK Tchem TRAF2 and NCK-interacting protein kinase 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAP3K10 Tchem Mitogen-activated protein kinase kinase kinase 10 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

LRRK2 Tchem Leucine-rich repeat serine/threonine-protein kinase 2 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAP3K11 Tchem Mitogen-activated protein kinase kinase kinase 11 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAP3K2 Tchem Mitogen-activated protein kinase kinase kinase 2 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ABL1 Tclin Tyrosine-protein kinase ABL1 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

MAP3K9 Tchem Mitogen-activated protein kinase kinase kinase 9 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 3-(1H-indol-5-yl)-5-[4-[(4-methylpiperazin-1-yl)methyl]phenyl]-1H-pyrrolo[2,3-b]pyridine
INCHI InChI=1S/C27H27N5/c1-31-10-12-32(13-11-31)18-19-2-4-20(5-3-19)23-15-24-25(17-30-27(24)29-16-23)21-6-7-26-22(14-21)8-9-28-26/h2-9,14-17,28H,10-13,18H2,1H3,(H,29,30)
InChi Key QKKIWEILHCXECO-UHFFFAOYSA-N
Canonical SMILES CN1CCN(CC1)CC2=CC=C(C=C2)C3=CC4=C(NC=C4C5=CC6=C(C=C5)NC=C6)N=C3
Isomeric SMILES CN1CCN(CC1)CC2=CC=C(C=C2)C3=CC4=C(NC=C4C5=CC6=C(C=C5)NC=C6)N=C3
PubChem CID 54764565
Molecular Weight 421.54

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Certificate of Analysis(COA)

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5 results found

Lot NumberCertificate TypeDateItem
I2222279Certificate of AnalysisJul 12, 2023 U275952
I2222280Certificate of AnalysisJul 12, 2023 U275952
I2222281Certificate of AnalysisJul 12, 2023 U275952
I2222282Certificate of AnalysisJul 12, 2023 U275952
I2222283Certificate of AnalysisJul 12, 2023 U275952

Chemical and Physical Properties

SolubilitySoluble in DMSO to 50 mM

Related Documents

References

1. Goodfellow VS, Loweth CJ, Ravula SB, Wiemann T, Nguyen T, Xu Y, Todd DE, Sheppard D, Pollack S, Polesskaya O et al..  (2013)  Discovery, synthesis, and characterization of an orally bioavailable, brain penetrant inhibitor of mixed lineage kinase 3..  J Med Chem,  56  (20): (8032-48).  [PMID:24044867]

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