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SHANGHAI SYSTEAM BIOCHEM CO., LTDCCG1423,
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CCG1423, CAS NO.285986-88-1

FOB Price:
USD 1.00-1.00 /Gram Get Latest Price
Min.Order Quantity:
100 Gram
Purity:
98%
Port:
shang hai
Payment Terms:
L/C

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Product Details

Keywords

  • CCG1423,
  • CCG-1423;N-(2-(4-Chloroanilino)-1-Methyl-2-oxoethoxy)-3,5-bis(trifluoroMethyl)benzaMide;N-(1-(4-chlorophenylaMino)-1-oxopropan-2-yloxy)-3,5-bis(trifluoroMethyl)benzaMide;N-({1-[(4-Chlorophenyl)Amino]-
  • 285986-88-1

Quick Details

  • ProName: CCG1423,
  • CasNo: 285986-88-1
  • Molecular Formula: C18H13ClF6N2O3
  • Appearance: White crystal
  • Application: CAS:285986-88-1; Small molecule inhib...
  • DeliveryTime: 2 months
  • PackAge: 100g,500g,1kg,25kg/drum
  • Port: shang hai
  • ProductionCapacity: 1000 Gram/Week
  • Purity: 98%
  • Storage: Dry seal
  • Transportation: shipping
  • LimitNum: 100 Gram

Superiority

we are specialized in custom synthesis, chemical/pharmaceutical/ pesticides outsourcing and contract research.
we are committed to provide excellence in researching, manufacturing and drug discovery process.
our research team of scientists consists of western-trained ph.d.s with experience and capabilities in drug r&d methodologies and medicinal chemistry.

Details

ccg-1423 is a novel inhibitor of rhoa/c-mediated gene transcription that is capable of inhibiting invasion of pc-3 prostate cancer cells in a matrigel model of metastasis.
ic50 value: 1.5 um [1]
target: rho signaling inhibitor
in vitro: ccg-1423 selectively inhibited spontaneous pc-3 prostate cancer cell invasion through a matrigel matrix, but not the gαi-dependent lpa-stimulated skov-3 ovarian cancer cell invasion, in vitro. at 100 μm, nearly complete inhibition of invasion was achieved with a lesser degree of toxicity than that induced by ccg-1423 at 10 μm [1]. srf binds to this site in vivo and the srf inhibitor ccg-1423 completely blocks stars proximal reporter activity in h9c2 cells [3]. pharmacological mkl-inhibition with ccg-1423 significantly inhibited ccn1 promoter activity as well as mrna and protein expression[4].
in vivo: pharmacological srf inhibition by ccg-1423 reduced nuclear mkl1 and improved glucose uptake and tolerance in insulin-resistant mice in vivo [2].

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