MedKoo Cat#: 597793 | Name: Ro 43-5054

Description:

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

Ro 43-5054 is a low molecular weight, noncyclic, peptidomimetic inhibitor.

Chemical Structure

Ro 43-5054
Ro 43-5054
CAS#138107-58-1

Theoretical Analysis

MedKoo Cat#: 597793

Name: Ro 43-5054

CAS#: 138107-58-1

Chemical Formula: C24H27N5O7

Exact Mass: 497.1910

Molecular Weight: 497.50

Elemental Analysis: C, 57.94; H, 5.47; N, 14.08; O, 22.51

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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Synonym
Ro 43-5054; Ro-43-5054; Ro43-5054; Ro 435054; Ro-435054; Ro435054;
IUPAC/Chemical Name
(S)-3-(3-(4-carbamimidoylbenzamido)propanamido)-4-(((S)-1-carboxy-2-phenylethyl)amino)-4-oxobutanoic acid
InChi Key
XPXOBWWMCFKOKQ-ROUUACIJSA-N
InChi Code
InChI=1S/C24H27N5O7/c25-21(26)15-6-8-16(9-7-15)22(33)27-11-10-19(30)28-17(13-20(31)32)23(34)29-18(24(35)36)12-14-4-2-1-3-5-14/h1-9,17-18H,10-13H2,(H3,25,26)(H,27,33)(H,28,30)(H,29,34)(H,31,32)(H,35,36)/t17-,18-/m0/s1
SMILES Code
O=C(O)[C@H](CC1=CC=CC=C1)NC([C@H](CC(O)=O)NC(CCNC(C2=CC=C(C(N)=N)C=C2)=O)=O)=O
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 497.50 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: Roux SP, Tschopp TB, Kuhn H, Steiner B, Hadváry P. Effects of heparin, aspirin and a synthetic platelet glycoprotein IIb-IIIa receptor antagonist (Ro 43-5054) on coronary artery reperfusion and reocclusion after thrombolysis with tissue-type plasminogen activator in the dog. J Pharmacol Exp Ther. 1993 Jan;264(1):501-8. PubMed PMID: 8423548. 2: Kouns WC, Kirchhofer D, Hadváry P, Edenhofer A, Weller T, Pfenninger G, Baumgartner HR, Jennings LK, Steiner B. Reversible conformational changes induced in glycoprotein IIb-IIIa by a potent and selective peptidomimetic inhibitor. Blood. 1992 Nov 15;80(10):2539-47. PubMed PMID: 1384788. 3: Xia Z, Frojmovic MM. Aggregation efficiency of activated normal or fixed platelets in a simple shear field: effect of shear and fibrinogen occupancy. Biophys J. 1994 Jun;66(6):2190-201. PubMed PMID: 8075353; PubMed Central PMCID: PMC1275945. 4: Wang XF, Liu F, Morris SA, Carroll RC. Synergistic outside-in regulation of platelet activation by GPIIb/IIIa ligand-induced conformation and oligomerization. Thromb Res. 2001 Nov 15;104(4):239-47. PubMed PMID: 11728525. 5: Murphy NP, Pratico D, Fitzgerald DJ. Functional relevance of the expression of ligand-induced binding sites in the response to platelet GP IIb/IIIa antagonists in vivo. J Pharmacol Exp Ther. 1998 Aug;286(2):945-51. PubMed PMID: 9694954. 6: Bernabei A, Gikakis N, Kowalska MA, Niewiarowski S, Edmunds LH Jr. Iloprost and echistatin protect platelets during simulated extracorporeal circulation. Ann Thorac Surg. 1995 Jan;59(1):149-53. PubMed PMID: 7529485. 7: Tanoue K, Katagiri Y, Suzuki H. Molecular mechanisms of fibrin gel clot retraction by platelets and cultured tumor cells. Pol J Pharmacol. 1996 May-Jun;48(3):341-3. PubMed PMID: 9112674. 8: Katagiri Y, Hiroyama T, Akamatsu N, Suzuki H, Yamazaki H, Tanoue K. Involvement of alpha v beta 3 integrin in mediating fibrin gel retraction. J Biol Chem. 1995 Jan 27;270(4):1785-90. PubMed PMID: 7530248.