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Ro 3306 - 98%, high purity , CAS No.872573-93-8, Inhibitor of cyclin dependent kinase 1;Inhibitor of cyclin dependent kinase 2;Inhibitor of cyclin dependent kinase 5

  • Moligand™
  • ≥98%
Item Number
R275210
Grouped product items
SKUSizeAvailabilityPrice Qty
R275210-1mg
1mg
In stock
$21.90
R275210-5mg
5mg
In stock
$90.90
R275210-25mg
25mg
In stock
$184.90
R275210-50mg
50mg
In stock
$276.90

Selective cyclin-dependent kinase (Cdk1) inhibitor

Basic Description

Synonyms(5Z)-5-(6-Quinolinylmethylene)-2-[(2-thienylmethyl)amino)-4(5H)-thiazolone
Specifications & Purity98%
SourceSynthetic
Storage TempStore at -20°C,Desiccated
Shipped InDry ice
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of cyclin dependent kinase 1;Inhibitor of cyclin dependent kinase 2;Inhibitor of cyclin dependent kinase 5
Product Description

Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months.

Associated Targets

CDK1 Tchem Cyclin-dependent kinase 1 2 Activities

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

CDK2 Tchem Cyclin-dependent kinase 2 2 Activities

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

CDK5 Tchem Cyclin-dependent-like kinase 5 1 Activities

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

Names and Identifiers

IUPAC Name (5Z)-5-(quinolin-6-ylmethylidene)-2-(thiophen-2-ylmethylimino)-1,3-thiazolidin-4-one
INCHI InChI=1S/C18H13N3OS2/c22-17-16(24-18(21-17)20-11-14-4-2-8-23-14)10-12-5-6-15-13(9-12)3-1-7-19-15/h1-10H,11H2,(H,20,21,22)/b16-10-
InChi Key XOLMRFUGOINFDQ-YBEGLDIGSA-N
Canonical SMILES C1=CC2=C(C=CC(=C2)C=C3C(=O)NC(=NCC4=CC=CS4)S3)N=C1
Isomeric SMILES C1=CC2=C(C=CC(=C2)/C=C\3/C(=O)NC(=NCC4=CC=CS4)S3)N=C1
PubChem CID 135400873
Molecular Weight 351.44

Certificates

Certificate of Analysis(COA)

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4 results found

Lot NumberCertificate TypeDateItem
G2208332Certificate of AnalysisApr 17, 2023 R275210
G2208333Certificate of AnalysisApr 17, 2023 R275210
G2208286Certificate of AnalysisApr 17, 2023 R275210
G2208235Certificate of AnalysisApr 17, 2023 R275210

Chemical and Physical Properties

Solubilityinsoluble in EtOH; insoluble in H2O; ≥4.39 mg/mL in DMSO
SensitivityHeat Sensitive

Related Documents

References

1. Vassilev LT, Tovar C, Chen S, Knezevic D, Zhao X, Sun H, Heimbrook DC, Chen L.  (2006)  Selective small-molecule inhibitor reveals critical mitotic functions of human CDK1..  Proc Natl Acad Sci USA,  103  (28): (10660-5).  [PMID:16818887]
2. Jorda R, Hendrychová D, Voller J, Řezníčková E, Gucký T, Kryštof V.  (2018)  How Selective Are Pharmacological Inhibitors of Cell-Cycle-Regulating Cyclin-Dependent Kinases?.  J Med Chem,  61  (20): (9105-9120).  [PMID:30234987]
3. Matsubara S et al..  (2020)  Fractionation of Ovarian Follicles and in vitro Oocyte Maturation and Ovulation Assay of Ciona intestinalis Type A..  Bio Protoc,  10  (7): (e3577).  [PMID:33659547]
4. Huang CR et al..  (2021)  Host CDK-1 and formin mediate microvillar effacement induced by enterohemorrhagic Escherichia coli..  Nat Commun,  12  (90).  [PMID:33397943]
5. Mukherjee A et al..  (2020)  Nuclear plasticity increases susceptibility to damage during confined migration..  PLoS Comput Biol,  16  (10): (e1008300).  [PMID:33035221]
6. Matsubara S et al..  (2019)  The regulation of oocyte maturation and ovulation in the closest sister group of vertebrates..  Elife,    [PMID:31573508]

Solution Calculators