FITM

CAS No. 932737-65-0

FITM( —— )

Catalog No. M20702 CAS No. 932737-65-0

FITM is a potent negative allosteric modulator of mGlu1 receptor(Ki : 2.5 nM).

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 35 In Stock
5MG 65 In Stock
10MG 110 In Stock
25MG 222 In Stock
50MG 368 In Stock
100MG 536 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    FITM
  • Note
    Research use only, not for human use.
  • Brief Description
    FITM is a potent negative allosteric modulator of mGlu1 receptor(Ki : 2.5 nM).
  • Description
    FITM is a potent negative allosteric modulator of mGlu1 receptor(Ki : 2.5 nM).
  • In Vitro
    FITM fits tightly into the long and narrow pocket. Most of the ligand-receptor interactions are hydrophobic with the exception of the contacts of the pyrimidine-amine group with the T815 7.38 side chain. The mGlu1 binding pocket for FITM largely corresponds to mutagenic data for the common allosteric site in mGlus and likely extends to other class C GPCRs. FITM which shows high affinity and selectivity for mGlu1 over mGlu5. FITM has the high hydrogen bonds occupancy with Thr815 and Tyr805 in dimer A and B of mGlu1 during molecular dynamics simulations. The nitrogen and hydrogen atoms of FITM form the dynamical hydrogen bonds with the hydrogen atom of Tyr805 and oxygen atom of Thr815, respectively. It indicates that there is a strong attraction interaction between FITM and allosteric sites.
  • In Vivo
    The pretreatment of rats with unlabeled FITM (1 mg/kg) occupies an mGluR1 binding site of 18F-FITM by more than 99% and does not affect the input function. The Kd (nM) and Bmax (pmol/mL) obtained by the Scatchard analyses with the multidose ligand assays are 2.1 and 36.3, respectively, for the thalamus; 2.1 and 27.5, respectively, for the hippocampus; 1.5 and 22.2, respectively, for the striatum; and 1.5 and 20.5, respectively, for the cingulate cortex with a high confidence. 18F-FITM shows excellent pharmacokinetics, namely the dense and specific accumulation in mGlu1-positive melanomas versus mGlu1-negative hepatoma and normal tissues. Furthermore, the accumulation levels of radioactivity corresponded to the extent of tumor and to levels of mGlu1 protein expression in melanomas and melanoma metastasis.
  • Synonyms
    ——
  • Pathway
    Neuroscience
  • Target
    GluR
  • Recptor
    mGluR1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    932737-65-0
  • Formula Weight
    371.43
  • Molecular Formula
    C18H18FN5OS
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:150 mg/mL (403.84 mM)
  • SMILES
    CC(C)Nc1cc(ncn1)-c1csc(n1)N(C)C(=O)c1ccc(F)cc1
  • Chemical Name
    4-Fluoro-N-[4-[6-(isopropylamino)pyrimidin-4-yl]-13-thiazol-2-yl]-N-methylbenzamide

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Hayes M Choudhary V Ojha N et al. Fat storage-inducing transmembrane (FIT or FITM) proteins are related to lipid phosphatase/phosphotransferase enzymes[J]. Microbial cell (Graz Austria) 2017 5(2):88.
molnova catalog
related products
  • L-Cysteinesulfinic a...

    L-Cysteinesulfinic acid monohydrate is a potent agonist at rat metabotropic glutamate receptors (mGluRs).

  • Ampalex

    Ampalex (Ampakine CX516; CX516; BDP 12) is an ampakine and nootropic that acts as an AMPA receptor positive allosteric modulator as a treatment for Alzheimer's disease.

  • VU6005649

    VU6005649 is an agonist of CNS penetrant mGlu7/8 receptor (EC50s: 0.65 μM and 2.6 μM for mGlu7 receptor and mGlu8 receptor, respectively).