MedKoo Cat#: 564320 | Name: ERW1041E

Description:

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

ERW1041E is a potent inhibitor of recombinant human and mouse Transglutaminase enzyme activity, mainly TG2 and the closely related enzyme TG1.

Chemical Structure

ERW1041E
ERW1041E
CAS#NONE

Theoretical Analysis

MedKoo Cat#: 564320

Name: ERW1041E

CAS#: NONE

Chemical Formula: C29H36

Exact Mass: 384.2817

Molecular Weight: 384.61

Elemental Analysis: C, 90.56; H, 9.44

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
ERW1041E; ERW-1041E; ERW 1041E;
IUPAC/Chemical Name
Quinolin-2-ylmethyl (S)-2-((((S)-3-bromo-4,5-dihydroisoxazol-5-yl)methyl)carbamoyl)pyrrolidine-1-carboxylate
InChi Key
JUUQCONZELUVJY-AZKAAPSKSA-N
InChi Code
InChI=1S/C29H36/c1-21-11-14-24(19-21)15-12-22(2)28-9-6-10-29(28)23(3)13-16-25-17-18-26-7-4-5-8-27(26)20-25/h4-5,7-8,11,17-18,20,24,28-29H,2-3,6,9-10,12-16,19H2,1H3/t24-,28+,29?/m1/s1
SMILES Code
C=C(C1[C@H](C(CC[C@@H]2CC(C)=CC2)=C)CCC1)CCC3=CC4=CC=CC=C4C=C3
Appearance
Solid powder
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
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 384.61 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: Chrobok NL, Bol JGJM, Jongenelen CA, Brevé JJP, El Alaoui S, Wilhelmus MMM, Drukarch B, van Dam AM. Characterization of Transglutaminase 2 activity inhibitors in monocytes in vitro and their effect in a mouse model for multiple sclerosis. PLoS One. 2018 Apr 24;13(4):e0196433. doi: 10.1371/journal.pone.0196433. eCollection 2018. PubMed PMID: 29689097; PubMed Central PMCID: PMC5918173. 2: Shinde AV, Su Y, Palanski BA, Fujikura K, Garcia MJ, Frangogiannis NG. Pharmacologic inhibition of the enzymatic effects of tissue transglutaminase reduces cardiac fibrosis and attenuates cardiomyocyte hypertrophy following pressure overload. J Mol Cell Cardiol. 2018 Apr;117:36-48. doi: 10.1016/j.yjmcc.2018.02.016. Epub 2018 Mar 2. PubMed PMID: 29481819; PubMed Central PMCID: PMC5892840. 3: Penumatsa KC, Toksoz D, Warburton RR, Kharnaf M, Preston IR, Kapur NK, Khosla C, Hill NS, Fanburg BL. Transglutaminase 2 in pulmonary and cardiac tissue remodeling in experimental pulmonary hypertension. Am J Physiol Lung Cell Mol Physiol. 2017 Nov 1;313(5):L752-L762. doi: 10.1152/ajplung.00170.2017. Epub 2017 Aug 3. PubMed PMID: 28775095; PubMed Central PMCID: PMC5792178. 4: Dafik L, Albertelli M, Stamnaes J, Sollid LM, Khosla C. Activation and inhibition of transglutaminase 2 in mice. PLoS One. 2012;7(2):e30642. doi: 10.1371/journal.pone.0030642. Epub 2012 Feb 2. PubMed PMID: 22319575; PubMed Central PMCID: PMC3271093.