MedKoo Cat#: 461941 | Name: Scopafungin

Description:

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

Scopafungin is a crystalline, nonpolyenic antimicrobial agent that is used as an antifungal.

Chemical Structure

Scopafungin
Scopafungin
CAS#11056-18-1 (free base),

Theoretical Analysis

MedKoo Cat#: 461941

Name: Scopafungin

CAS#: 11056-18-1 (free base),

Chemical Formula: C59H103N3O18

Exact Mass: 1141.7237

Molecular Weight: 1142.47

Elemental Analysis: C, 62.03; H, 9.09; N, 3.68; O, 25.21

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.
Bulk Inquiry
Related CAS #
11056-18-1 (free base) 116296-63-0 (malonate)
Synonym
Scopafungin; N-29479; N 29479; N29479; Nificin; U 29479; U-29479; U29479;
IUPAC/Chemical Name
3-oxo-3-(((10E,12Z,20E)-5,7,9,19,23,25,27,31,33,34,35-undecahydroxy-8,14,18,22,26,30-hexamethyl-15-((E)-4-methyl-12-(3-methylguanidino)dodec-8-en-2-yl)-17-oxo-16,37-dioxabicyclo[31.3.1]heptatriaconta-10,12,20-trien-3-yl)oxy)propanoic acid
InChi Key
VAYOSPAPALLOIO-GTGIXXMMSA-N
InChi Code
InChI=1S/C59H103N3O18/c1-34(18-14-12-10-11-13-17-25-62-58(60)61-9)26-38(5)55-37(4)19-15-16-20-45(64)39(6)49(68)28-42(63)27-43(78-54(74)32-53(72)73)29-44-30-51(70)56(75)59(77,80-44)33-52(71)36(3)22-23-46(65)40(7)50(69)31-48(67)35(2)21-24-47(66)41(8)57(76)79-55/h10-11,15-16,19-21,24,34-52,55-56,63-71,75,77H,12-14,17-18,22-23,25-33H2,1-9H3,(H,72,73)(H3,60,61,62)/b11-10+,19-15-,20-16+,24-21+
SMILES Code
O=C(OC(CC(O)CC(O)C(C)C(O)/C=C/C=C\C(C)C(C(C)CC(C)CCC/C=C/CCCNC(NC)=N)O1)CC(O2)CC(O)C(O)C2(O)CC(O)C(C)CCC(O)C(C)C(O)CC(O)C(C)/C=C/C(O)C(C)C1=O)CC(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
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 1,142.47 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: Takesako K, Nakamura T, Obayashi A, Iwasaki S, Namikoshi M, Okuda S, Beppu T. Demalonyl derivatives of azalomycin F4 and scopafungin. J Antibiot (Tokyo). 1986 May;39(5):713-6. PubMed PMID: 3733520. 2: Johnson LE, Dietz A. Scopafungin, a crystalline antibiotic produced by Streptomyces hygroscopicus var. enhygrus var. nova. Appl Microbiol. 1971 Sep;22(3):303-8. PubMed PMID: 4940870; PubMed Central PMCID: PMC376304. 3: Reusser F. Scopafungin, an inhibitor of oxidative phosphorylation in mitochondria. Biochem Pharmacol. 1972 Apr 1;21(7):1031-8. PubMed PMID: 4339110. 4: Bergy ME, Hoeksema H. Scopafungin, a crystalline endomycin component. J Antibiot (Tokyo). 1972 Jan;25(1):39-43. PubMed PMID: 5010644. 5: Mogi T, Matsushita K, Murase Y, Kawahara K, Miyoshi H, Ui H, Shiomi K, Omura S, Kita K. Identification of new inhibitors for alternative NADH dehydrogenase (NDH-II). FEMS Microbiol Lett. 2009 Feb;291(2):157-61. doi: 10.1111/j.1574-6968.2008.01451.x. Epub 2008 Dec 5. PubMed PMID: 19076229. 6: Dolak LA, Reusser F, Baczynskyj L, Mizsak SA, Hannon BR, Castle TM. Desertomycin: purification and physical-chemical properties. J Antibiot (Tokyo). 1983 Jan;36(1):13-9. PubMed PMID: 6678910. 7: Kumazawa S, Asami Y, Awane K, Ohtani H, Fukuchi C, Mikawa T, Hayase T. Structural studies of new macrolide antibiotics, shurimycins A and B. J Antibiot (Tokyo). 1994 Jun;47(6):688-96. PubMed PMID: 8040074. 8: Stefanelli S, Corti E, Montanini N, Denaro M, Sarubbi E. Inhibitors of type-I interleukin-1 receptor from microbial metabolites. J Antibiot (Tokyo). 1997 Jun;50(6):484-9. PubMed PMID: 9268004. 9: Kuimova TF, Kazakov GA, Inshakova TA. [Spontaneous crystallization of antibiotic substance during submerged fermentation of Actinomyces hygroscopicus]. Mikrobiologiia. 1976 JUL-AUG;45(4):746-9. Russian. PubMed PMID: 979694.