MedKoo Cat#: 208407 | Name: Narmafotinib
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Description:

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

Narmafotinib (AMP-945) is a selective and potent inhibitor of focal adhesion kinase (FAK), developed for oncology and fibrosis-related indications. It targets FAK with nanomolar potency (reported IC₅₀ ~1–5 nM in biochemical assays) and exhibits high selectivity over other kinases. Preclinical studies have shown that AMP-945 effectively reduces phosphorylation of FAK and downstream signaling molecules such as paxillin and AKT in cancer cell lines and fibrotic models. In xenograft tumor models, AMP-945 has demonstrated antitumor activity, particularly when combined with chemotherapy or immune checkpoint inhibitors, supporting its role in modifying the tumor microenvironment

Chemical Structure

Narmafotinib
Narmafotinib
CAS# 1393653-34-3

Theoretical Analysis

MedKoo Cat#: 208407

Name: Narmafotinib

CAS#: 1393653-34-3

Chemical Formula: C28H32F3N5O2

Exact Mass: 527.2508

Molecular Weight: 527.59

Elemental Analysis: C, 63.74; H, 6.11; F, 10.80; N, 13.27; O, 6.06

Price and Availability

Size Price Availability Quantity
25mg USD 1,950.00 2 Weeks
50mg USD 2,950.00 2 Weeks
100mg USD 3,950.00 2 Weeks
200mg USD 5,650.00 2 Weeks
500mg USD 7,950.00 2 Weeks
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Related CAS #
1393653-34-3
Synonym
AMP-945; AMP 945; AMP945; Narmafotinib
IUPAC/Chemical Name
2-[2-[2-[2-[2-Methoxy-4-(1-methylpiperidin-4-yl)anilino]-5-(trifluoromethyl)pyrimidin-4-yl]ethyl]phenyl]acetamide
InChi Key
AWJVIOYPZZZYAX-UHFFFAOYSA-N
InChi Code
InChI=1S/C28H32F3N5O2/c1-36-13-11-19(12-14-36)21-8-10-24(25(15-21)38-2)35-27-33-17-22(28(29,30)31)23(34-27)9-7-18-5-3-4-6-20(18)16-26(32)37/h3-6,8,10,15,17,19H,7,9,11-14,16H2,1-2H3,(H2,32,37)(H,33,34,35)
SMILES Code
O=C(N)CC1=CC=CC=C1CCC2=NC(NC3=CC=C(C4CCN(C)CC4)C=C3OC)=NC=C2C(F)(F)F
Appearance
To be determined
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
To be determined
Shelf Life
>2 years if stored properly
Drug Formulation
To be determined
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

Preparing Stock Solutions

The following data is based on the product molecular weight 527.59 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
[1]. Street I, et al. Abstract LB-308: combination of CTx-0294945 a highly selective inhibitor of focal adhesion kinase with bevacizumab in pre-clinical models of breast cancer[J]. Cancer Research, 2012, 72(8_Supplement): LB-308-LB-308. https://aacrjournals.org/cancerres/article/72/8_Supplement/LB-308/583555