Bivittoside A | CAS#77394-03-7 | antifungal agent

MedKoo Cat#: 598322 | Name: Bivittoside A

Description:

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

Bivittoside A is an antifungal agent.

Chemical Structure

Bivittoside A

CAS#77394-03-7

Theoretical Analysis

MedKoo Cat#: 598322

Name: Bivittoside A

CAS#: 77394-03-7

Chemical Formula: C41H67O13

Exact Mass: 767.4582

Molecular Weight: 767.97

Elemental Analysis: C, 64.12; H, 8.79; O, 27.08

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

Bivittoside A;

IUPAC/Chemical Name

(3S,5R,8R,10S,12S,13R,17S)-3-(((2S,3R,4S,5R)-4,5-dihydroxy-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-12-hydroxy-17-((S)-2-hydroxy-6-methylheptan-2-yl)-4,4,10,14-tetramethyl-1,2,3,4,5,6,7,8,10,12,14,15,16,17-tetradecahydro-14l5-14,13-(epoxymethano)cyclopenta[a]phenanthren-19-one

InChi Key

HUMSPESDMWWCRJ-BCUNVWNOSA-N

InChi Code

InChI=1S/C41H67O13/c1-20(2)10-9-15-39(7,49)26-14-17-41(8)23-11-12-25-37(4,5)28(13-16-38(25,6)22(23)18-27(43)40(26,41)36(48)54-41)52-35-33(30(45)24(42)19-50-35)53-34-32(47)31(46)29(44)21(3)51-34/h18,20-21,23-35,42-47,49H,9-17,19H2,1-8H3/t21-,23-,24-,25+,26-,27+,28+,29-,30+,31+,32-,33-,34+,35+,38-,39+,40+/m1/s1

SMILES Code

CC1(C)[C@@H](O[C@H]2[C@@H]([C@H]([C@@H](CO2)O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@@H](C)O3)O)O)O)CC[C@]4(C)C5=C[C@H](O)[C@]6(C(O7)=O)[C@@H]([C@@](C)(O)CCCC(C)C)CCC67(C)[C@]5([H])CC[C@@]14[H]

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 767.97 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: Lakshmi V, Srivastava S, Mishra SK, Shukla PK. Antifungal activity of bivittoside-D from Bohadschia vitiensis (Semper). Nat Prod Res. 2012;26(10):913-8. doi: 10.1080/14786419.2010.534096. Epub 2011 Aug 2. PubMed PMID: 21809953. 2: Omran NE, Khedr AM. Structure elucidation, protein profile and the antitumor effect of the biological active substance extracted from sea cucumber Holothuria polii. Toxicol Ind Health. 2015 Jan;31(1):1-8. doi: 10.1177/0748233712466135. Epub 2012 Nov 27. PubMed PMID: 23188650. 3: Yuan WH, Yi YH, Tang HF, Liu BS, Wang ZL, Sun GQ, Zhang W, Li L, Sun P. Antifungal triterpene glycosides from the sea cucumber Bohadschia marmorata. Planta Med. 2009 Feb;75(2):168-73. doi: 10.1055/s-0028-1088348. Epub 2008 Dec 18. PubMed PMID: 19096993. 4: Hill JA, Szabat M, Hoesli CA, Gage BK, Yang YH, Williams DE, Riedel MJ, Luciani DS, Kalynyak TB, Tsai K, Ao Z, Andersen RJ, Warnock GL, Piret JM, Kieffer TJ, Johnson JD. A multi-parameter, high-content, high-throughput screening platform to identify natural compounds that modulate insulin and Pdx1 expression. PLoS One. 2010 Sep 23;5(9):e12958. doi: 10.1371/journal.pone.0012958. PubMed PMID: 20886041; PubMed Central PMCID: PMC2944895. 5: Lakshmi V, Saxena A, Mishra SK, Raghubir R, Srivastava MN, Jain RK, Maikhuri JP, Gupta G. Spermicidal activity of bivittoside D from Bohadschia vitiensis. Arch Med Res. 2008 Oct;39(7):631-8. doi: 10.1016/j.arcmed.2008.06.007. PubMed PMID: 18760190. 6: Honey-Escandón M, Arreguín-Espinosa R, Solís-Marín FA, Samyn Y. Biological and taxonomic perspective of triterpenoid glycosides of sea cucumbers of the family Holothuriidae (Echinodermata, Holothuroidea). Comp Biochem Physiol B Biochem Mol Biol. 2015 Feb;180:16-39. doi: 10.1016/j.cbpb.2014.09.007. Epub 2014 Sep 28. Review. PubMed PMID: 25263252. 7: Wang Z, Gong W, Sun G, Tang H, Liu B, Li L, Yi Y, Zhang W. New holostan-type triterpene glycosides from the sea cucumber Apostichopus japonicus. Nat Prod Commun. 2012 Nov;7(11):1431-4. PubMed PMID: 23285801. 8: Yu BS, Jo IH. Interaction of sea cucumber saponins with multilamellar liposomes. Chem Biol Interact. 1984 Dec;52(2):185-202. PubMed PMID: 6509686. 9: Sun P, Liu BS, Yi YH, Li L, Gui M, Tang HF, Zhang DZ, Zhang SL. A new cytotoxic lanostane-type triterpene glycoside from the sea cucumber Holothuria impatiens. Chem Biodivers. 2007 Mar;4(3):450-7. PubMed PMID: 17372947.