MedKoo Cat#: 414667 | Name: Oxeclosporin

Description:

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

Oxeclosporin is a hydroxyethyl derivative of serine(8)-cyclosporine; inhibits proliferation and functions of lymphocytes.

Chemical Structure

Oxeclosporin
Oxeclosporin
CAS#135548-15-1

Theoretical Analysis

MedKoo Cat#: 414667

Name: Oxeclosporin

CAS#: 135548-15-1

Chemical Formula: C64H115N11O14

Exact Mass: 1261.8625

Molecular Weight: 1262.69

Elemental Analysis: C, 60.88; H, 9.18; N, 12.20; O, 17.74

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
Oxeclosporin; Sdz imm 125
IUPAC/Chemical Name
(3S,6S,9S,12R,15S,18S,21S,24S,30S,33S)-30-ethyl-33-((1R,2R,E)-1-hydroxy-2-methylhex-4-en-1-yl)-12-((2-hydroxyethoxy)methyl)-6,9,18,24-tetraisobutyl-3,21-diisopropyl-1,4,7,10,15,19,25,28-octamethyl-1,4,7,10,13,16,19,22,25,28,31-undecaazacyclotritriacontan-2,5,8,11,14,17,20,23,26,29,32-undecaone
InChi Key
XZDDMPMZGYEESG-VNHFGJPGSA-N
InChi Code
InChI=1S/C64H115N11O14/c1-24-26-27-42(15)54(78)53-58(82)66-44(25-2)59(83)69(17)34-50(77)70(18)46(30-36(3)4)57(81)68-51(40(11)12)63(87)71(19)47(31-37(5)6)56(80)65-43(16)55(79)67-45(35-89-29-28-76)60(84)72(20)48(32-38(7)8)61(85)73(21)49(33-39(9)10)62(86)74(22)52(41(13)14)64(88)75(53)23/h24,26,36-49,51-54,76,78H,25,27-35H2,1-23H3,(H,65,80)(H,66,82)(H,67,79)(H,68,81)/b26-24+/t42-,43+,44+,45-,46+,47+,48+,49+,51+,52+,53+,54-/m1/s1
SMILES Code
CC[C@@H]1NC([C@@H](N(C([C@@H](N(C([C@@H](N(C([C@@H](N(C([C@H](NC([C@@H](NC([C@@H](N(C([C@H](C(C)C)NC([C@@H](N(C(CN(C1=O)C)=O)C)CC(C)C)=O)=O)C)CC(C)C)=O)C)=O)COCCO)=O)C)CC(C)C)=O)C)CC(C)C)=O)C)C(C)C)=O)C)[C@@H]([C@@H](C/C=C/C)C)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
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 1,262.69 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: Billich A, Vyplel H, Grassberger M, Schmook FP, Steck A, Stuetz A. Novel cyclosporin derivatives featuring enhanced skin penetration despite increased molecular weight. Bioorg Med Chem. 2005 May 2;13(9):3157-67. doi: 10.1016/j.bmc.2005.02.049. PMID: 15809151. 2: Hiestand PC, Gräber M, Hurtenbach U, Herrmann P, Cammisuli S, Richardson BP, Eberle MK, Donatsch P, Ryffel B, Borel JF. New cyclosporine derivative SDZ IMM 125: in vitro and in vivo pharmacologic effects and toxicologic evaluation. Transplant Proc. 1993 Feb;25(1 Pt 1):691-2. PMID: 8438439. 3: Vickers AE, Meyer E, Dannecker R, Keller B, Tynes RE, Maurer G. Human liver cytochrome P4503A biotransformation of the cyclosporin derivative SDZ IMM 125. Drug Metab Dispos. 1995 Mar;23(3):321-6. PMID: 7628296. 4: Vickers AE, Jimenez RM, Spaans MC, Pflimlin V, Fisher RL, Brendel K. Human and rat lung biotransformation of cyclosporin A and its derivatives using slices and bronchial epithelial cells. Drug Metab Dispos. 1997 Jul;25(7):873-80. PMID: 9224782. 5: Kawai R, Lemaire M, Steimer JL, Bruelisauer A, Niederberger W, Rowland M. Physiologically based pharmacokinetic study on a cyclosporin derivative, SDZ IMM 125. J Pharmacokinet Biopharm. 1994 Oct;22(5):327-65. doi: 10.1007/BF02353860. PMID: 7791036. 6: Witkamp L, Zonneveld IM, Jung EG, Schopf RE, Christophers E, Grossman R, Meffert H, Belaich S, Mahrle G, Van Joost T, et al. Efficacy and tolerability of multiple-dose SDZ IMM 125 in patients with severe psoriasis. Br J Dermatol. 1995 Jul;133(1):95-103. doi: 10.1111/j.1365-2133.1995.tb02500.x. PMID: 7669649. 7: Vickers AE, Alegret M, Meyer E, Smiley S, Guertler J. Hydroxyethyl cyclosporin A induces and decreases P4503A and P-glycoprotein levels in rat liver. Xenobiotica. 1996 Jan;26(1):27-39. doi: 10.3109/00498259609046686. PMID: 8851819. 8: Bruelisauer A, Kawai R, Misslin P, Lemaire M. Absorption and disposition of SDZ IMM 125, a new cyclosporine derivative, in rats after single and repeated administration. Drug Metab Dispos. 1994 Mar-Apr;22(2):194-9. PMID: 8013274. 9: Vickers AE, Fisher RL, Brendel K, Guertler J, Dannecker R, Keller B, Fischer V. Sites of biotransformation for the cyclosporin derivative SDZ IMM 125 using human liver and kidney slices and intestine. Comparison with rat liver slices and cyclosporin A metabolism. Drug Metab Dispos. 1995 Mar;23(3):327-33. PMID: 7628297. 10: Grub S, Trommer WE, Wolf A. Role of antioxidants in the O-hydroxyethyl-D-(Ser)8-cyclosporine A (SDZ IMM125)-induced apoptosis in rat hepatocytes. Biochem Pharmacol. 2002 Dec 15;64(12):1725-36. doi: 10.1016/s0006-2952(02)01384-9. PMID: 12445861.