901730-21-0

TACR1-IN-1 Chemical Structure
901730-21-0

Chemical Structure

TACR1-IN-1

  • CAS No.: 901730-21-0
  • Formula:C23H24FN3O3
  • Molecular Weight:409.45

InChIKey: TYDFSQYEDVHERH-UHFFFAOYSA-N

SMILES: FC1=CC=C(N2CCN(C(COC3=CC(N(CC)C4=CC=CC=C43)=O)=O)CC2)C=C1

Biological Activity: TACR1-IN-1 is a TACR1 inhibitor. TACR1-IN-1 attenuates Substance P-driven ERK phosphorylation and downstream malignant programs. TACR1-IN-1 reduces PGP9.5-positive tumor innervation in orthotopic PDAC models. TACR1-IN-1 increases antigen presentation and immune chemokine-related transcript expression under Substance P treatment conditions. TACR1-IN-1 reverses Substance P-associated reduction in Gemcitabine (HY-17026) sensitivity. TACR1-IN-1 can be used for research on pancreatic ductal adenocarcinoma[1].

Cat. No. Product Name Purity Description Pricing
HY-189358
TACR1-IN-1 TACR1-IN-1 is a TACR1 inhibitor. TACR1-IN-1 attenuates Substance P-driven ERK phosphorylation and downstream malignant programs. TACR1-IN-1 reduces PGP9.5-positive tumor innervation in orthotopic PDAC models. TACR1-IN-1 increases antigen presentation and immune chemokine-related transcript expression under Substance P treatment conditions. TACR1-IN-1 reverses Substance P-associated reduction in Gemcitabine (HY-17026) sensitivity. TACR1-IN-1 can be used for research on pancreatic ductal adenocarcinoma.
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This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References