Stachartin A

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Stachartin A
Category Others
Catalog number BBF-04395
CAS 1978388-54-3
Molecular Weight 428.56
Molecular Formula C26H36O5
Purity 98.0%

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BBF-04395 1 mg $629 In stock

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Description

Stachartin A is produced in the cultures of the tin mine tailings-associated fungus Stachybotrys chartarum.

Specification

Synonyms Stachybotrysin; 3-Buten-2-one, 4-[(1'R,2'R,4'aS,6'R,8'aS)-3',4',4'a,5',6',7',8',8'a-octahydro-4,6'-dihydroxy-6-(hydroxymethyl)-2',5',5',8'a-tetramethylspiro[benzofuran-2(3H), 1'(2'H)-naphthalen]-7-yl]-, (3E)-
Storage Store at -20°C
IUPAC Name (E)-4-[(3R,4aS,7R,8R,8aS)-3,4'-dihydroxy-6'-(hydroxymethyl)-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,2'-3H-1-benzofuran]-7'-yl]but-3-en-2-one
Canonical SMILES CC1CCC2C(C(CCC2(C13CC4=C(C=C(C(=C4O3)C=CC(=O)C)CO)O)C)O)(C)C
InChI InChI=1S/C26H36O5/c1-15-6-9-21-24(3,4)22(30)10-11-25(21,5)26(15)13-19-20(29)12-17(14-27)18(23(19)31-26)8-7-16(2)28/h7-8,12,15,21-22,27,29-30H,6,9-11,13-14H2,1-5H3/b8-7+/t15-,21+,22-,25+,26-/m1/s1
InChI Key WHSVMLKIVYFFBS-DTCCPBINSA-N

Properties

Appearance Powder
Boiling Point 617.3±55.0°C (Predicted)
Density 1.22±0.1 g/cm3 (Predicted)
Solubility Soluble in Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone

Reference Reading

1. Rational quality assessment procedure for less-investigated herbal medicines: Case of a Congolese antimalarial drug with an analytical report
Dieudonné Tshitenge Tshitenge, Karine Ndjoko Ioset, José Nzunzu Lami, Josaphat Ndelo-di-Phanzu, Jean-Pierre Koy Sita Mufusama, Gerhard Bringmann Fitoterapia. 2016 Apr;110:189-95. doi: 10.1016/j.fitote.2016.03.012. Epub 2016 Mar 20.
Herbal medicines are the most globally used type of medical drugs. Their high cultural acceptability is due to the experienced safety and efficiency over centuries of use. Many of them are still phytochemically less-investigated, and are used without standardization or quality control. Choosing SIROP KILMA, an authorized Congolese antimalarial phytomedicine, as a model case, our study describes an interdisciplinary approach for a rational quality assessment of herbal drugs in general. It combines an authentication step of the herbal remedy prior to any fingerprinting, the isolation of the major constituents, the development and validation of an HPLC-DAD analytical method with internal markers, and the application of the method to several batches of the herbal medicine (here KILMA) thus permitting the establishment of a quantitative fingerprint. From the constitutive plants of KILMA, acteoside, isoacteoside, stachannin A, and pectolinarigenin-7-O-glucoside were isolated, and acteoside was used as the prime marker for the validation of an analytical method. This study contributes to the efforts of the WHO for the establishment of standards enabling the analytical evaluation of herbal materials. Moreover, the paper describes the first phytochemical and analytical report on a marketed Congolese phytomedicine.

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