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Documenti fondamentali

SMB01016

Sigma-Aldrich

Pomolic acid

≥90% (LC/MS-ELSD)

Sinonimo/i:

19α-Hydroxyursolic acid, Benthamic acid, Randialic acid A

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1 MG
414,00 €

About This Item

Formula empirica (notazione di Hill):
C30H48O4
Numero CAS:
Peso molecolare:
472.70
Numero MDL:
Codice UNSPSC:
12352205
NACRES:
NA.25

414,00 €


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Origine biologica

plant

Saggio

≥90% (LC/MS-ELSD)

Stato

solid

PM

472.7

Solubilità

water: slightly soluble

applicazioni

metabolomics
vitamins, nutraceuticals, and natural products

Temperatura di conservazione

−20°C

Stringa SMILE

O[C@]1([C@@H]2[C@@](CC[C@]3([C@]4([C@@H]([C@@]5([C@H](C([C@H](CC5)O)(C)C)CC4)C)CC=C32)C)C)(CC[C@H]1C)C(=O)O)C

InChI

1S/C30H48O4/c1-18-10-15-30(24(32)33)17-16-27(5)19(23(30)29(18,7)34)8-9-21-26(4)13-12-22(31)25(2,3)20(26)11-14-28(21,27)6/h8,18,20-23,31,34H,9-17H2,1-7H3,(H,32,33)/t18-,20+,21-,22+,23-,26+,27-,28-,29-,30+/m1/s1
ZZTYPLSBNNGEIS-OPAXANQDSA-N

Descrizione generale

Natural product derived from plant source.
Pomolic acid, a pentacyclic triterpene, is a bioactive natural compound commonly derived from plants such as Euscaphis japonica, Centella asiatica, Picramnia sellowii, and Cecropia pachystachya. Current research suggests that this metabolite acts as an inhibitor and may exhibit diverse biological activities, including anticancer, anti-inflammatory, antiviral, apoptotic, and antihypertensive properties.

Applicazioni

Pomolic acid is a natural product derived from plant source that finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Azioni biochim/fisiol

Pomolic acid is highly effective in inhibiting cell growth and inducing apoptosis.

Caratteristiche e vantaggi

  • Suitable for Biochemical and Biomedical research
  • Versatile and adaptable for wide variety of laboratory and research applications

Altre note

For additional information on our range of Biochemicals, please complete this form.

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable


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Certificati d'analisi (COA)

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Guillermo Schinella et al.
Planta medica, 74(3), 215-220 (2008-02-09)
The dichloromethane extract and pomolic acid ( 5) obtained from leaves of Cecropia pachystachya both reduced carrageenan-induced paw oedema in mice. Interestingly, while the triterpenoid inhibited the in vivo production of interleukin-1beta by 39 %, it had no effect on
Y Kashiwada et al.
Journal of natural products, 61(9), 1090-1095 (1998-09-28)
Oleanolic acid (1) was identified as an anti-HIV principle from several plants, including Rosa woodsii (leaves), Prosopis glandulosa (leaves and twigs), Phoradendron juniperinum (whole plant), Syzygium claviflorum (leaves), Hyptis capitata (whole plant), and Ternstromia gymnanthera (aerial part). It inhibited HIV-1
Studies on constituents of medicinal plants. XIII. Constituents of the pericarps of the capsules of Euscaphis japonica Pax.
K Takahashi et al.
Chemical & pharmaceutical bulletin, 22(3), 650-653 (1974-03-01)
Phuong Thien Thuong et al.
Biological & pharmaceutical bulletin, 29(4), 830-833 (2006-04-06)
A new ursane-type triterpenoid, weigelic acid (1), and seven known compounds, ursolic acid (2), ilekudinol A (3), corosolic acid (4), ilekudinol B (5), esculentic acid (6), pomolic acid (7), and asiatic acid (8) were isolated from the leaf and stem

Domande

Recensioni

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