Cucumechinoside C | CAS#125640-32-6 | bioactive natural chemical

MedKoo Cat#: 598329 | Name: Cucumechinoside C

Description:

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

Cucumechinoside C is a bioactive natural chemical.

Chemical Structure

Cucumechinoside C

CAS#125640-32-6

Theoretical Analysis

MedKoo Cat#: 598329

Name: Cucumechinoside C

CAS#: 125640-32-6

Chemical Formula: C54H86O28S2

Exact Mass: 1246.4747

Molecular Weight: 1247.37

Elemental Analysis: C, 52.00; H, 6.95; O, 35.91; S, 5.14

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 #

No Data

Synonym

Cucumechinoside C;

IUPAC/Chemical Name

((2R,3S,4S,5S,6S)-6-(((2R,3R,4R,5S,6R)-4,5-dihydroxy-6-(((2R,3R,4S,5R)-4-hydroxy-2-(((3R,3aS,5aS,7aS,9R,11aR,11bS,13aS)-3,5a,8,8,11a-pentamethyl-3-(4-methyl-2-oxopentyl)-1-oxo-3a,4,5,5a,7,7a,8,9,10,11,11a,11b,12,13-tetradecahydro-1H,3H-naphtho[2',1':4,5]indeno[1,7a-c]furan-9-yl)oxy)-5-(sulfooxy)tetrahydro-2H-pyran-3-yl)oxy)-2-methyltetrahydro-2H-pyran-3-yl)oxy)-4-(((2S,3R,4R,5R,6S)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxytetrahydro-2H-pyran-2-yl)oxy)-3,5-dihydroxytetrahydro-2H-pyran-2-yl)methyl hydrogen sulfate

InChi Key

SUKVYAYIZXRRBY-SOACPDBGSA-N

InChi Code

InChI=1S/C54H86O28S2/c1-23(2)18-25(56)19-53(8)32-13-16-52(7)27-10-11-31-50(4,5)33(14-15-51(31,6)26(27)12-17-54(32,52)49(64)81-53)77-48-44(36(59)30(21-72-48)82-84(68,69)70)80-45-38(61)37(60)41(24(3)74-45)78-47-40(63)43(35(58)29(76-47)22-73-83(65,66)67)79-46-39(62)42(71-9)34(57)28(20-55)75-46/h10,23-24,26,28-48,55,57-63H,11-22H2,1-9H3,(H,65,66,67)(H,68,69,70)/t24-,26-,28+,29-,30-,31-,32-,33-,34-,35+,36-,37-,38+,39-,40+,41+,42-,43+,44-,45-,46+,47+,48-,51-,52+,53-,54-/m1/s1

SMILES Code

O[C@H]1[C@@H](COS(O)(=O)=O)O[C@@H](O[C@@H]2[C@H](O)[C@H](O)[C@H](O[C@@H]2C)O[C@@H]3[C@H](O)[C@H](OS(=O)(O)=O)CO[C@@H]3O[C@@H]4CC[C@]5(C)[C@@H]6CC[C@@]78[C@@](C)(CC[C@@H]7[C@@](C)(CC(CC(C)C)=O)OC8=O)C6=CC[C@@H]5C4(C)C)[C@@H](O)[C@H]1O[C@@H]9O[C@@H](CO)[C@@H](O)[C@@H](OC)[C@H]9O

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

Instruction

View handling instruction

Preparing Stock Solutions

The following data is based on the product molecular weight 1,247.37 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.

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: Flaherty DW, Hibbitts DD, Iglesia E. Metal-catalyzed C-C bond cleavage in alkanes: effects of methyl substitution on transition-state structures and stability. J Am Chem Soc. 2014 Jul 9;136(27):9664-76. doi: 10.1021/ja5037429. Epub 2014 Jun 25. PubMed PMID: 24961991. 2: Basso AV, Nicotra VE, Parra A, Martínez A, Fernández-Vivas A. Biotransformation of Salpichrolides A, C, and G by Three Filamentous Fungi. J Nat Prod. 2016 Jun 24;79(6):1658-67. doi: 10.1021/acs.jnatprod.6b00310. Epub 2016 Jun 10. PubMed PMID: 27285201. 3: Yamada M, Tanabe Y, Dang JS, Sato S, Mizorogi N, Hachiya M, Suzuki M, Abe T, Kurihara H, Maeda Y, Zhao X, Lian Y, Nagase S, Akasaka T. D(2d)(23)-C(84) versus Sc(2)C(2)@D(2d)(23)-C(84): Impact of Endohedral Sc(2)C(2) Doping on Chemical Reactivity in the Photolysis of Diazirine. J Am Chem Soc. 2016 Dec 21;138(50):16523-16532. doi: 10.1021/jacs.6b10751. Epub 2016 Dec 7. PubMed PMID: 27998084. 4: Filho LC, Packer L. Revision of the Neotropical subgenera Coelioxys (Platycoelioxys) Mitchell and C. (Rhinocoelioxys) Mitchell (Hymenoptera; Megachilidae) with the description of one new species. Zootaxa. 2015 Mar 31;3941(2):151-203. doi: 10.11646/zootaxa.3941.2.1. PubMed PMID: 25947503. 5: Bai Y, Li S, Zong YN, Li XL, Zhao ZH, Kong XD. [Mutation screening of 433 families with Duchenne/Becker muscular dystrophy]. Zhonghua Yi Xue Za Zhi. 2016 Apr 26;96(16):1261-9. doi: 10.3760/cma.j.issn.0376-2491.2016.16.008. Chinese. PubMed PMID: 27122458. 6: Zhang H, Timmermann BN. Withanolide Structural Revisions by (13)C NMR Spectroscopic Analysis Inclusive of the γ-Gauche Effect. J Nat Prod. 2016 Apr 22;79(4):732-42. doi: 10.1021/acs.jnatprod.5b00648. Epub 2016 Feb 19. PubMed PMID: 26894655. 7: Henderson SJ, Timbs AT, McCarthy J, Gallienne AE, Proven M, Rugless MJ, Lopez H, Eglinton J, Dziedzic D, Beardsall M, Khalil MS, Old JM. Ten Years of Routine α- and β-Globin Gene Sequencing in UK Hemoglobinopathy Referrals Reveals 60 Novel Mutations. Hemoglobin. 2016;40(2):75-84. doi: 10.3109/03630269.2015.1113990. Epub 2015 Dec 4. Review. PubMed PMID: 26635043. 8: Ding L, Ishida N, Murakami M, Morokuma K. sp3-sp2 vs sp3-sp3 C-C site selectivity in Rh-catalyzed ring opening of benzocyclobutenol: a DFT study. J Am Chem Soc. 2014 Jan 8;136(1):169-78. doi: 10.1021/ja407422q. Epub 2013 Dec 16. PubMed PMID: 24341735. 9: Pavuluri CM, Kawamura K. Enrichment of (13)C in diacids and related compounds during photochemical processing of aqueous aerosols: New proxy for organic aerosols aging. Sci Rep. 2016 Nov 4;6:36467. doi: 10.1038/srep36467. PubMed PMID: 27811980; PubMed Central PMCID: PMC5095555. 10: Clark JS, Yang G, Osnowski AP. Synthesis of the C-1-C-17 fragment of amphidinolides C, C2, C3, and F. Org Lett. 2013 Apr 5;15(7):1460-3. doi: 10.1021/ol4004838. Epub 2013 Mar 25. PubMed PMID: 23527702. 11: Wen Y, Huang L, Jiang H. Access to C(sp3)-C(sp2) and C(sp2)-C(sp2) bond formation via sequential intermolecular carbopalladation of multiple carbon-carbon bonds. J Org Chem. 2012 Jun 15;77(12):5418-22. doi: 10.1021/jo300662x. Epub 2012 Jun 5. PubMed PMID: 22647071. 12: Milde B, Schaarschmidt D, Rüffer T, Lang H. Phosphino imidazoles and imidazolium salts for Suzuki C-C coupling reactions. Dalton Trans. 2012 May 7;41(17):5377-90. doi: 10.1039/c2dt12322c. Epub 2012 Mar 27. PubMed PMID: 22450875. 13: Hou H, Wang C, Sun F, Zhao L, Dun A, Sun Z. Association of interleukin-6 gene polymorphism with coronary artery disease: an updated systematic review and cumulative meta-analysis. Inflamm Res. 2015 Sep;64(9):707-20. doi: 10.1007/s00011-015-0850-9. Epub 2015 Jul 15. Review. PubMed PMID: 26174156. 14: Xu X, Jia J, Sun H, Liu Y, Xu W, Shi Y, Zhang D, Li X. Selective activation of C-F and C-H bonds with iron complexes, the relevant mechanism study by DFT calculations and study on the chemical properties of hydrido iron complex. Dalton Trans. 2013 Mar 14;42(10):3417-28. doi: 10.1039/c2dt31795h. Epub 2012 Dec 20. PubMed PMID: 23258248. 15: Shi L, Tao YF, Shi L, Yao YF, Yu L, Lin KQ, Huang XQ, Yi W, Sun H, Chu JY. [Distribution of HLA-C genes and HLA C-B, A-C-B haplotypes in Jinuo, Maonan and Wa ethnic populations in southwest China]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Jun;28(3):341-6. doi: 10.3760/cma.j.issn.1003-9406.2011.03.023. Chinese. PubMed PMID: 21644237. 16: Foetisch K, Dahl L, Jansen B, Becker WM, Lidholm J, van Ree R, Broll H, Kaul S, Vieths S, Holzhauser T. Development and in-house validation of allergen-specific ELISA tests for the quantification of Dau c 1.01, Dau c 1.02 and Dau c 4 in carrot extracts (Daucus carota). Anal Bioanal Chem. 2011 Jan;399(2):935-43. doi: 10.1007/s00216-010-4348-6. Epub 2010 Nov 3. PubMed PMID: 21046078. 17: Harpale A, Panesi M, Chew HB. Communication: Surface-to-bulk diffusion of isolated versus interacting C atoms in Ni(111) and Cu(111) substrates: A first principle investigation. J Chem Phys. 2015 Feb 14;142(6):061101. doi: 10.1063/1.4907716. PubMed PMID: 25681880. 18: Gupta S, Verma M, Singh K. Does LDL-C Estimation Using Anandaraja's Formula Give a Better Agreement with Direct LDL-C Estimation than the Friedewald's Formula? Indian J Clin Biochem. 2012 Apr;27(2):127-33. doi: 10.1007/s12291-011-0186-3. Epub 2012 Mar 24. PubMed PMID: 23543806; PubMed Central PMCID: PMC3358371. 19: Pinto H, Tissue DT, Ghannoum O. Panicum milioides (C(3)-C(4)) does not have improved water or nitrogen economies relative to C(3) and C(4) congeners exposed to industrial-age climate change. J Exp Bot. 2011 May;62(9):3223-34. doi: 10.1093/jxb/err005. Epub 2011 Feb 9. PubMed PMID: 21307386. 20: Werner H, Wiedemann R, Laubender M, Windmüller B, Steinert P, Gevert O, Wolf J. Unusual pathways for metal-assisted C[bond]C and C[bond]P coupling reactions using allenylidenerhodium complexes as precursors. J Am Chem Soc. 2002 Jun 19;124(24):6966-80. PubMed PMID: 12059220.