MedKoo Cat#: 562433 | Name: Tie2-IN-5
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Tie2-IN-5 is a selective inhibitor of the Tie2 receptor, a receptor tyrosine kinase primarily expressed on endothelial cells and involved in vascular development and angiogenesis. By targeting Tie2, Tie2-IN-5 modulates vascular stability and endothelial cell function, making it a potential therapeutic agent for diseases characterized by abnormal angiogenesis, such as cancer and diabetic retinopathy. Research on Tie2-IN-5 explores its role in regulating blood vessel formation, inflammation, and tumor growth, with applications in cancer therapy and other angiogenesis-related conditions.

Chemical Structure

Tie2-IN-5
Tie2-IN-5
CAS#948557-43-5

Theoretical Analysis

MedKoo Cat#: 562433

Name: Tie2-IN-5

CAS#: 948557-43-5

Chemical Formula: C26H21N3O2S

Exact Mass: 439.1354

Molecular Weight: 439.53

Elemental Analysis: C, 71.05; H, 4.82; N, 9.56; O, 7.28; S, 7.29

Price and Availability

Size Price Availability Quantity
10mg USD 265.00 2 Weeks
25mg USD 450.00 2 Weeks
50mg USD 800.00 2 Weeks
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Synonym
Tie2-IN-5; Tie2 IN 5; Tie2IN5; Tie2 inhibitor 5; Tie2-inhibitor-5; Tie2 kinase inhibitor 5; Compound 5;
IUPAC/Chemical Name
4-[4-(6-Methoxy-2-naphthalenyl)-2-[4-(methylsulfinyl)phenyl]-1H-imidazol-5-yl]pyridine
InChi Key
SINQIEAULQKUPD-UHFFFAOYSA-N
InChi Code
InChI=1S/C26H21N3O2S/c1-31-22-8-5-19-15-21(4-3-20(19)16-22)25-24(17-11-13-27-14-12-17)28-26(29-25)18-6-9-23(10-7-18)32(2)30/h3-16H,1-2H3,(H,28,29)
SMILES Code
O=S(C1=CC=C(C2=NC(C3=CC=C4C=C(OC)C=CC4=C3)=C(C5=CC=NC=C5)N2)C=C1)C
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 439.53 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: El-Damasy AK, Cho NC, Nam G, Pae AN, Keum G. Discovery of a Nanomolar Multikinase Inhibitor (KST016366): A New Benzothiazole Derivative with Remarkable Broad-Spectrum Antiproliferative Activity. ChemMedChem. 2016 Aug 5;11(15):1587-95. doi: 10.1002/cmdc.201600224. Epub 2016 Jul 12. PubMed PMID: 27405013. 2: Wang HC, Chang FR, Huang TJ, Kuo CY, Tsai YC, Wu CC. (-)-Liriopein B Suppresses Breast Cancer Progression via Inhibition of Multiple Kinases. Chem Res Toxicol. 2015 May 18;28(5):897-906. doi: 10.1021/tx500518j. Epub 2015 Apr 21. PubMed PMID: 25856345. 3: Semones M, Feng Y, Johnson N, Adams JL, Winkler J, Hansbury M. Pyridinylimidazole inhibitors of Tie2 kinase. Bioorg Med Chem Lett. 2007 Sep 1;17(17):4756-60. Epub 2007 Jun 27. PubMed PMID: 17618114. 4: Gingrich DE, Reddy DR, Iqbal MA, Singh J, Aimone LD, Angeles TS, Albom M, Yang S, Ator MA, Meyer SL, Robinson C, Ruggeri BA, Dionne CA, Vaught JL, Mallamo JP, Hudkins RL. A new class of potent vascular endothelial growth factor receptor tyrosine kinase inhibitors: structure-activity relationships for a series of 9-alkoxymethyl-12-(3-hydroxypropyl)indeno[2,1-a]pyrrolo[3,4-c]carbazole-5-ones and the identification of CEP-5214 and its dimethylglycine ester prodrug clinical candidate CEP-7055. J Med Chem. 2003 Dec 4;46(25):5375-88. PubMed PMID: 14640546.