MedKoo Cat#: 574844 | Name: PD 173955-Analog1
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Description:

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

PD 173955-Analog1 is a potent c-Src inhibitor known to have activity against a variety of cancers including colon, lung, head and neck carcinoma.

Chemical Structure

PD 173955-Analog1
PD 173955-Analog1
CAS#185039-99-0

Theoretical Analysis

MedKoo Cat#: 574844

Name: PD 173955-Analog1

CAS#: 185039-99-0

Chemical Formula: C21H14Cl2N4O3

Exact Mass: 440.0443

Molecular Weight: 441.27

Elemental Analysis: C, 57.16; H, 3.20; Cl, 16.07; N, 12.70; O, 10.88

Price and Availability

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5mg USD 650.00 2 Weeks
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Related CAS #
No Data
Synonym
PD 173955-Analog1
IUPAC/Chemical Name
3-[[6-(2,6-Dichlorophenyl)-7,8-dihydro-8-methyl-7-oxopyrido[2,3-d]pyrimidin-2-yl]amino]benzoic Acid
InChi Key
RBURTLAMOSHNGX-UHFFFAOYSA-N
InChi Code
InChI=1S/C21H14Cl2N4O3/c1-27-18-12(9-14(19(27)28)17-15(22)6-3-7-16(17)23)10-24-21(26-18)25-13-5-2-4-11(8-13)20(29)30/h2-10H,1H3,(H,29,30)(H,24,25,26)
SMILES Code
O=C(O)C1=CC=CC(NC2=NC=C(C=C(C3=C(Cl)C=CC=C3Cl)C(N4C)=O)C4=N2)=C1
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
>3 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
Product Data
Biological target:
PD 173955-Analog1 is a potent c-Src inhibitor.
In vitro activity:
TBD
In vivo activity:
TBD

Preparing Stock Solutions

The following data is based on the product molecular weight 441.27 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
Formulation protocol:
TBD
In vitro protocol:
TBD
In vivo protocol:
TBD
1. Zhang J, Wang S, Jiang B, Huang L, Ji Z, Li X, Zhou H, Han A, Chen A, Wu Y, Ma H, Zhao W, Zhao Q, Xie C, Sun X, Zhou Y, Huang H, Suleman M, Lin F, Zhou L, Tian F, Jin M, Cai Y, Zhang N, Li Q. c-Src phosphorylation and activation of hexokinase promotes tumorigenesis and metastasis. Nat Commun. 2017 Jan 5;8:13732. doi: 10.1038/ncomms13732. PMID: 28054552; PMCID: PMC5227066. 2. Lou L, Yu Z, Wang Y, Wang S, Zhao Y. c-Src inhibitor selectively inhibits triple-negative breast cancer overexpressed Vimentin in vitro and in vivo. Cancer Sci. 2018 May;109(5):1648-1659. doi: 10.1111/cas.13572. Epub 2018 Apr 17. PMID: 29575318; PMCID: PMC5980174. 3. Li J, Hu B, Wang T, Huang W, Ma C, Zhao Q, Zhuo L, Zhang T, Jiang Y. C-Src confers resistance to mitotic stress through inhibition DMAP1/Bub3 complex formation in pancreatic cancer. Mol Cancer. 2018 Dec 15;17(1):174. doi: 10.1186/s12943-018-0919-5. Erratum in: Mol Cancer. 2019 Nov 29;18(1):172. PMID: 30553276; PMCID: PMC6295060.