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

MedKoo CAT#: 406405

CAS#: 669764-17-4

Description: SU11606 is a potent c-MET inhibitor with potential anticancer activity.

Chemical Structure

CAS# 669764-17-4

Theoretical Analysis

MedKoo Cat#: 406405
Name: SU11606
CAS#: 669764-17-4
Chemical Formula: C29H33ClN4O4S
Exact Mass: 568.1911
Molecular Weight: 569.11472
Elemental Analysis: C, 61.20; H, 5.84; Cl, 6.23; N, 9.84; O, 11.25; S, 5.63

Size Price Shipping out time Quantity
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Pricing updated 2021-03-05. Prices are subject to change without notice.

SU11606 is not in stock, may be available through custom synthesis. For cost-effective reason, minimum 1 gram order is requested. The product will be characterized by NMR, HPLC and MS analysis. Purity (HPLC) is usually >98%. CoA, QC data, MSDS will be provided when product is successfully made. The estimated lead time is 2-3 months. Please send email to to inquire quote.

Synonym: SU11606; SU 11606; SU11606.

IUPAC/Chemical Name: (Z)-N-(3-chlorophenyl)-3-((3,5-dimethyl-4-(3-morpholinopropyl)-1H-pyrrol-2-yl)methylene)-N-methyl-2-oxoindoline-5-sulfonamide


InChi Code: InChI=1S/C29H33ClN4O4S/c1-19-24(8-5-11-34-12-14-38-15-13-34)20(2)31-28(19)18-26-25-17-23(9-10-27(25)32-29(26)35)39(36,37)33(3)22-7-4-6-21(30)16-22/h4,6-7,9-10,16-18,31H,5,8,11-15H2,1-3H3,(H,32,35)/b26-18-

SMILES Code: O=S(C1=CC2=C(NC(/C2=C\C3=C(C)C(CCCN4CCOCC4)=C(C)N3)=O)C=C1)(N(C5=CC=CC(Cl)=C5)C)=O

yellow solid powder

>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).

Soluble in DMSO, not in water

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:

Handling Instructions:

Preparing Stock Solutions

The following data is based on the product molecular weight 569.11472 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.

Select a batch to recalculate based on the batch molecular weight:
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

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1. Golub, Todd; Straussman, Ravid. Methods of treating cancer using a chemotherapeutic agent with an agent that blocks the activity of hepatocyte growth factor or its cognate receptor c-MET. From PCT Int. Appl. (2012), WO 2012178038 A1 20121227.

2. Smith, David; Hussain, Maha. Dual inhibitors of Met and VEGF for the treatment of castration resistant prostate cancer and osteoblastic bone metastases. PCT Int. Appl. (2012), WO 2012044577 A1 20120405

3. Comoglio, Paolo Maria; Vigna, Elisa; Giordano, Silvia. Use of monoclonal antibody (AntiMET-R) directed against hepatocyte growth factor receptor (HGFR) for the treatment and diagnosis of tumors. PCT Int. Appl. (2007), WO 2007090807 A1 20070816.

4. Tang, Peng Cho; Liang, Congxin; Miller, Todd; Lipson, Kenneth E. Preparation of 5-sulfonamido-substituted indolinone compounds as protein kinase inhibitors. U.S. Pat. Appl. Publ. (2004), US 20040204407 A1 20041014

5. Wang, Xueyan; Le, Phuong; Liang, Congxin; Chan, Julie; Kiewlich, David; Miller, Todd; Harris, Dave; Sun, Li; Rice, Audie; Vasile, Stefan; et al. Potent and selective inhibitors of the Met [hepatocyte growth factor/scatter factor (HGF/SF) receptor] tyrosine kinase block HGF/SF-induced tumor cell growth and invasion. Molecular Cancer Therapeutics (2003), 2(11), 1085-1092.

Additional Information