Arbortristoside A | CAS# 97145-52-3 | Anti-nociceptive

MedKoo Cat#: 573224 | Name: Arbortristoside A

Description:

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

Arbortristoside A is an anti-inflammatory and antinociceptive. This activity may be due to the inhibiting effect of prostaglandin, histamine and serotonin. Arbortristoside A has also been shown to act on ulcerations and may facilitate healing of peptic ulcers.

Chemical Structure

Arbortristoside A

CAS#97145-52-3

Theoretical Analysis

MedKoo Cat#: 573224

Name: Arbortristoside A

CAS#: 97145-52-3

Chemical Formula: C27H34O13

Exact Mass: 566.1999

Molecular Weight: 566.56

Elemental Analysis: C, 57.24; H, 6.05; O, 36.71

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 #

97145-52-3

Synonym

Arbortristoside A

IUPAC/Chemical Name

Cyclopenta(c)pyran-4-carboxylic acid, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-6-hydroxy-5-((3-(4-methoxyphenyl)-1-oxo-2-propenyl)oxy)-7-methyl-, methyl ester, (1S-(1alpha,4aalpha,5alpha(E),6alpha,7alpha,7aalpha))-

InChi Key

OQNPBHSDFWPQEK-IIJMSXQASA-N

InChi Code

1S/C27H34O13/c1-12-18-19(24(20(12)30)39-17(29)9-6-13-4-7-14(35-2)8-5-13)15(25(34)36-3)11-37-26(18)40-27-23(33)22(32)21(31)16(10-28)38-27/h4-9,11-12,16,18-24,26-28,30-33H,10H2,1-3H3/b9-6+/t12?,16-,18?,19-,20?,21-,22+,23-,24?,26+,27+/m1/s1

SMILES Code

C=1([C@@H]2[C@@H]([C@@H](OC1)O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)[C@@H]([C@@H]([C@@H]2OC(\C=C\c1ccc(cc1)OC)=O)O)C)C(=O)OC

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

Instruction

View handling instruction

Preparing Stock Solutions

The following data is based on the product molecular weight 566.56 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: Pandeti S, Sharma K, Bathula SR, Tadigoppula N. Synthesis of novel anticancer iridoid derivatives and their cell cycle arrest and caspase dependent apoptosis. Phytomedicine. 2014 Feb 15;21(3):333-9. doi: 10.1016/j.phymed.2013.08.023. Epub 2013 Sep 25. PubMed PMID: 24075214. 2: Mishra V, Shukla A, Pandeti S, Barthwal MK, Pandey HP, Palit G, Narender T. Arbortristoside-A and 7-O-trans-cinnamoyl-6β-hydroxyloganin isolated from Nyctanthes arbortristis possess anti-ulcerogenic and ulcer-healing properties. Phytomedicine. 2013 Sep 15;20(12):1055-63. doi: 10.1016/j.phymed.2013.04.010. Epub 2013 Jun 7. PubMed PMID: 23746957. 3: Das S, Sasmal D, Basu SP. Anti-inflammatory and antinociceptive activity of arbortristoside-A. J Ethnopharmacol. 2008 Feb 28;116(1):198-203. doi: 10.1016/j.jep.2007.11.034. Epub 2007 Nov 29. PubMed PMID: 18178352. 4: Gupta P, Bajpai SK, Chandra K, Singh KL, Tandon JS. Antiviral profile of Nyctanthes arbortristis L. against encephalitis causing viruses. Indian J Exp Biol. 2005 Dec;43(12):1156-60. PubMed PMID: 16359127.