MedKoo Cat#: 412800 | Name: Chasmanine

Description:

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

Chasmanine is an alkaloid isolated from the roots of Aconitum crassicaule with anti-inflammatory pharmacodynamic components

Chemical Structure

Chasmanine
Chasmanine
CAS#5066-78-4

Theoretical Analysis

MedKoo Cat#: 412800

Name: Chasmanine

CAS#: 5066-78-4

Chemical Formula: C25H41NO6

Exact Mass: 451.2934

Molecular Weight: 451.60

Elemental Analysis: C, 66.49; H, 9.15; N, 3.10; O, 21.26

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 #
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Synonym
Chasmanine; Toroko base II; Chasmanin
IUPAC/Chemical Name
1-ethyl-6,10,13-trimethoxy-3-(methoxymethyl)tetradecahydro-11aH-3,6a,12-(epiethane[1,1,2]triyl)-7,9-methanonaphtho[2,3-b]azocine-8,11a-diol
InChi Key
DBODJJZRZFZBBD-UHFFFAOYSA-N
InChi Code
InChI=1S/C25H41NO6/c1-6-26-11-23(12-29-2)8-7-16(31-4)25-14-9-13-15(30-3)10-24(28,17(14)19(13)27)18(22(25)26)20(32-5)21(23)25/h13-22,27-28H,6-12H2,1-5H3
SMILES Code
CCN1CC2(CCC(C34C5CC6C(C5C(CC6OC)(C(C14)C(C23)OC)O)O)OC)COC
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
>2 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 451.60 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: Yang B, Han Y, Zhang QY, Dong H, Sun H, Wang XJ. [Study on absorbed components of Aconitum kusnezoffii under Yunnan Baiyao compatibility in effect of activating blood circulation and removing blood stasis]. Zhongguo Zhong Yao Za Zhi. 2019 Aug;44(15):3349-3357. Chinese. doi: 10.19540/j.cnki.cjcmm.20190711.202. PMID: 31602894. 2: Xu Y, Li Y, Zhang P, Yang B, Wu H, Guo X, Li Y, Zhang Y. Sensitive UHPLC- MS/MS quantitation and pharmacokinetic comparisons of multiple alkaloids from Fuzi- Beimu and single herb aqueous extracts following oral delivery in rats. J Chromatogr B Analyt Technol Biomed Life Sci. 2017 Jul 15;1058:24-31. doi: 10.1016/j.jchromb.2017.05.016. Epub 2017 May 15. PMID: 28528229. 3: Zhu M, Liu XY, Chen QH, Wang FP. Biomimetic conversion of aconitine-type C19-diterpenoid alkaloids to lactone-type alkaloids. J Asian Nat Prod Res. 2012;14(5):441-9. doi: 10.1080/10286020.2012.669378. PMID: 22530673. 4: Gao F, Li YY, Wang D, Huang X, Liu Q. Diterpenoid alkaloids from the Chinese traditional herbal "Fuzi" and their cytotoxic activity. Molecules. 2012 May 4;17(5):5187-94. doi: 10.3390/molecules17055187. PMID: 22628040; PMCID: PMC6268201. 5: Liu ZL, Cao J, Zhang HM, Lin LL, Liu HJ, Du SS, Zhou L, Deng ZW. Feeding deterrents from Aconitum episcopale roots against the red flour beetle, Tribolium castaneum. J Agric Food Chem. 2011 Apr 27;59(8):3701-6. doi: 10.1021/jf104879h. Epub 2011 Mar 18. PMID: 21417277. 6: Díaz JG, Ruiz JG, de La Fuente G. Alkaloids from Delphinium staphisagria. J Nat Prod. 2000 Aug;63(8):1136-9. doi: 10.1021/np990453l. PMID: 10978212. 7: Fengpeng W, Qicheng F. Alkaloids from roots of Aconitum crassicaule. Planta Med. 1981 Aug;42(8):375-9. doi: 10.1055/s-2007-971658. PMID: 17401992. 8: Yang J, Liu W, Yang X, Zhao J, Liu F, Li L. [Diterpenoid alkaloids from Aconitum handelianum]. Zhongguo Zhong Yao Za Zhi. 2009 Aug;34(15):1927-9. Chinese. PMID: 19894536. 9: Sun Q, Cao H, Zhou Y, Wang X, Jiang H, Gong L, Yang Y, Rong R. Qualitative and quantitative analysis of the chemical constituents in Mahuang-Fuzi-Xixin decoction based on high performance liquid chromatography combined with time-of- flight mass spectrometry and triple quadrupole mass spectrometers. Biomed Chromatogr. 2016 Nov;30(11):1820-1834. doi: 10.1002/bmc.3758. Epub 2016 Jul 5. PMID: 27183898. 10: Zhou XL, Chen QH, Chen DL, Wang FP. Hemsleyatine, a novel C19-diterpenoid alkaloid with 8-amino group from Aconitum hemsleyanum. Chem Pharm Bull (Tokyo). 2003 May;51(5):592-4. doi: 10.1248/cpb.51.592. PMID: 12736463.