MedKoo Cat#: 598380 | Name: Lantanolic acid

Description:

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

Lantanolic acid is a new pentacyclic triterpenoid from the leaves of Lantana montevidensis.

Chemical Structure

Lantanolic acid
Lantanolic acid
CAS#32303-26-7

Theoretical Analysis

MedKoo Cat#: 598380

Name: Lantanolic acid

CAS#: 32303-26-7

Chemical Formula: C30H46O4

Exact Mass: 470.3396

Molecular Weight: 470.69

Elemental Analysis: C, 76.55; H, 9.85; O, 13.60

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 #
No Data
Synonym
Lantanolic acid;
IUPAC/Chemical Name
(3S,4aR,6aR,6bS,8aS,12aS,14aS,14bS)-3-hydroxy-4,4,6a,6b,11,11-hexamethyl-2,3,4,4a,5,6,6a,7,8,9,10,11,12,12a,14,14a-hexadecahydro-1H-3,14b-(epoxymethano)picene-8a(6bH)-carboxylic acid
InChi Key
UFVGYQQCHANGSN-SSLXYFFCSA-N
InChi Code
InChI=1S/C30H46O4/c1-24(2)11-13-28(23(31)32)14-12-26(5)19(20(28)17-24)7-8-22-27(26,6)10-9-21-25(3,4)30(33)16-15-29(21,22)18-34-30/h7,20-22,33H,8-18H2,1-6H3,(H,31,32)/t20-,21-,22-,26+,27+,28-,29+,30-/m0/s1
SMILES Code
CC1(C)[C@]2(O)CC[C@]3(CO2)[C@@]4([H])CC=C5[C@]6([H])CC(C)(C)CC[C@@](C(O)=O)6CC[C@](C)5[C@@](C)4CC[C@@]13[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

Preparing Stock Solutions

The following data is based on the product molecular weight 470.69 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: Makboul MA, Attia AA, Farag SF, Mohamed NM, Ross SA, Takaya Y, Niwa M. A new pentacyclic triterpenoid from the leaves of Lantana montevidensis (Spreng.) Briq. Nat Prod Res. 2013;27(21):2046-52. doi: 10.1080/14786419.2013.824443. Epub 2013 Aug 21. PubMed PMID: 23961713. 2: Dat NT, Lee IS, Cai XF, Shen G, Kim YH. Oleanane triterpenoids with inhibitory activity against NFAT transcription factor from Liquidambar formosana. Biol Pharm Bull. 2004 Mar;27(3):426-8. PubMed PMID: 14993816. 3: Barre JT, Bowden BF, Coll JC, DeJesus J, De La Fuente VE, Janairo GC, Ragasa CY. A bioactive triterpene from Lantana camara. Phytochemistry. 1997 May;45(2):321-4. PubMed PMID: 9162177. 4: Begum S, Zehra SQ, Siddiqui BS, Fayyaz S, Ramzan M. Pentacyclic triterpenoids from the aerial parts of Lantana camara and their nematicidal activity. Chem Biodivers. 2008 Sep;5(9):1856-66. doi: 10.1002/cbdv.200890173. PubMed PMID: 18816515. 5: Pan WD, Li YJ, Mai LT, Ohtani KH, Kasai RT, Tanaka O, Yu DQ. [Studies on triterpenoid constituents of the roots of Lantana camara]. Yao Xue Xue Bao. 1993;28(1):40-4. Chinese. PubMed PMID: 8328269. 6: Begum S, Wahab A, Siddiqui BS. Pentacyclic triterpenoids from the aerial parts of Lantana camara. Chem Pharm Bull (Tokyo). 2003 Feb;51(2):134-7. PubMed PMID: 12576645. 7: Chiu CL, Lee TH, Shao YY, Kuo YH. Three new triterpenes from the roots of Rhus javanica L. var. roxburghiana. J Asian Nat Prod Res. 2008 Jul-Aug;10(7-8):693-7. doi: 10.1080/10286020802016446. PubMed PMID: 18636383. 8: Wächter GA, Valcic S, Franzblau SG, Suarez E, Timmermann BN. Antitubercular activity of triterpenoids from Lippia turbinata. J Nat Prod. 2001 Jan;64(1):37-41. PubMed PMID: 11170663. 9: Qamar F, Begum S, Raza SM, Wahab A, Siddiqui BS. Nematicidal natural products from the aerial parts of Lantana camara Linn. Nat Prod Res. 2005 Sep;19(6):609-13. PubMed PMID: 16010828.