Free shipping on all orders over $ 500

EIPA

Cat. No. M6705
EIPA Structure
Synonym:

L593754; MH 12-43; Ethylisopropylamiloride

Size Price Availability Quantity
10mM*1mL in DMSO USD 52  USD52 In stock
5mg USD 50  USD50 In stock
10mg USD 78  USD78 In stock
50mg USD 276  USD276 In stock
Free Delivery on orders over USD 500 Bulk Inquiry?

Quality Control & Documentation
Biological Activity

EIPA is a tRPP3 channel inhibitor (IC50 = 10.5 μM). EIPA inhibits the Na+/H+ exchanger (NHE). EIPA inhibits macropinocytosis as well. EIPA can be used in the research of inflammation and cancers, such as gastric cancer, colon carcinoma, pancreatic carcinoma.

Chemical Information
Molecular Weight 299.76
Formula C11H18ClN7O
CAS Number 1154-25-2
Solubility (25°C) DMSO 45 mg/mL
1eq. HCl: 10 mg/mL
Storage Powder -20°C
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] Hemstapat, et al. Mol Pharmacol. A novel class of positive allosteric modulators of metabotropic glutamate receptor subtype 1 interact with a site distinct from that of negative allosteric modulators.

Related TRP Channel Products
N-Oleoyl glutamine

N-oleoyl-glutamine is a PM20D1-regulated N-acyl amino acids (NAAs).

N-Oleoyl valine

N-Oleoyl valine is a N-acyl valine compound that acts as a TRPV3 receptor antagonist.

TAT-M2NX

TAT-M2NX (tatM2NX) is a TRPM2 inhibitor with specific neuroprotective activity in male mice.

SOR-C13

SOR-C13, a carboxy-terminal truncated peptide, is a high-affinity TRPV6 antagonist with an IC50 value of 14 nM.

GsMTx4 TFA

GsMTx4 TFA is a spider venom peptide that selectively inhibits cation permeable mechanosensitive channels (MSCs) belonging to the Piezo and TRP channel families. In addition, GsMTx4 TFA blocks cation-selective stretch-activated channels (SACs) and attenuates lysophosphatidylcholine (LPC)-induced astrocytotoxicity and microglial cell reactivity.

  Catalog
Abmole Inhibitor Catalog




Keywords: EIPA, L593754; MH 12-43; Ethylisopropylamiloride supplier, TRP Channel, inhibitors, activators


Products are for research use only. Not for human use. We do not sell to patients.
© Copyright 2010-2023 AbMole BioScience. All Rights Reserved.