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  • DC Chemicals Limited
  • China
  • Product Name: Manool
  • Price: $Inquiry/250mg $Inquiry/100mg $Inquiry/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

596-85-0

596-85-0 structure
596-85-0 structure
  • Name: Manool
  • Chemical Name: manool
  • CAS Number: 596-85-0
  • Molecular Formula: C20H34O
  • Molecular Weight: 290.48300
  • Catalog: Natural product Lignans
  • Create Date: 2018-09-17 13:39:12
  • Modify Date: 2024-01-03 10:57:15
  • Manool is a diterpene from Salvia officinalis. Manool induces selective cytotoxicity in cancer cells. Manool arrests the cancer cells at the G(2)/M phase of the cell cycle[1][2].

Name manool
Synonyms 8,14-labdadien-13-ol
MFCD01310996
MANOOL
Description Manool is a diterpene from Salvia officinalis. Manool induces selective cytotoxicity in cancer cells. Manool arrests the cancer cells at the G(2)/M phase of the cell cycle[1][2].
Related Catalog
In Vitro Manool exhibits higher cytotoxic activity against HeLa (IC50=6.7 µg/mL) and U343 (IC50=6.7 µg/mL) cells[1]. Manool exhibits a protective effect against chromosome damage induced by MMS in HepG2 cells[3].
References

[1]. de Oliveira PF, et al. Manool, a Salvia officinalis diterpene, induces selective cytotoxicity in cancer cells. Cytotechnology. 2016;68(5):2139-2143.

[2]. Pratsinis H, et al. Antiproliferative activity of Greek propolis. J Med Food. 2010;13(2):286-290.

[3]. Nicolella HD, et al. Differential effect of manool--a diterpene from Salvia officinalis, on genotoxicity induced by methyl methanesulfonate in V79 and HepG2 cells. Food Chem Toxicol. 2014;72:8-12.

Density 0.93g/cm3
Boiling Point 368.2ºC at 760mmHg
Melting Point 49-52ºC(lit.)
Molecular Formula C20H34O
Molecular Weight 290.48300
Flash Point 118.2ºC
Exact Mass 290.26100
PSA 20.23000
LogP 5.50240
Index of Refraction 1.5
Hazard Codes Xi: Irritant;
Risk Phrases R36/37/38
Safety Phrases S26-S36
WGK Germany 3

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Literature: Rogachev, Victor; Loehl, Thorsten; Markert, Thomas; Metz, Peter Arkivoc, 2012 , vol. 2012, # 3 p. 172 - 180

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Literature: Organic and Biomolecular Chemistry, , vol. 9, # 7 p. 2156 - 2165

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Literature: Arkivoc, , vol. 2012, # 3 p. 172 - 180

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Literature: Arkivoc, , vol. 2012, # 3 p. 172 - 180

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Literature: Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, , vol. 26, # 1-12 p. 453 - 458

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Literature: Agricultural and Biological Chemistry, , vol. 46, # 10 p. 2477 - 2484

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Detail
Literature: Justus Liebigs Annalen der Chemie, , vol. 617, p. 134 Journal of the Chemical Society, , p. 2187,2189