202415-99-4
202415-99-4
Chemical Structure
HMR-4011A
Synonym(s): IPL 576092
- CAS No.: 202415-99-4
- Formula:C21H34O3
- Molecular Weight:334.49
IUPAC Name: (3S,5S,6R,7R,8R,9S,10R,13S,14S,Z)-17-ethylidene-10,13-dimethylhexadecahydro-1H-cyclopenta[a]phenanthrene-3,6,7-triol
InChIKey: MBRMDGSBOOLIGQ-QYJZNYBASA-N
SMILES: O[C@@H]1[C@]2([H])[C@@](CC[C@@]3(C)[C@@]2([H])CC/C3=C/C)([H])[C@]4(C)[C@@](C[C@@H](O)CC4)([H])[C@H]1O
Biological Activity: HMR-4011A (IPL 576092) is an orally active, chemically modified version of Contignasterol. HMR-4011A can be isolated from sponge Petrosia contignata. HMR-4011A reduces inflammation. HMR-4011A can be used in the research of asthma[1][2][3].
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HMR-4011A | HMR-4011A (IPL 576092) is an orally active, chemically modified version of Contignasterol. HMR-4011A can be isolated from sponge Petrosia contignata. HMR-4011A reduces inflammation. HMR-4011A can be used in the research of asthma. | |||||||||||||||||||||
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References
- [1]. Thoms C, et al. Biotechnological potential of marine sponges and their associated bacteria as producers of new pharmaceuticals (part I). 2005.
- [2]. Singh R, et al. Clinical status of anti-cancer agents derived from marine sources. Anticancer Agents Med Chem. 2008 Aug;8(6):603-17. [Content Brief]
- [3]. Galeano E, et al. Pharmacological developments obtained from marine natural products and current pipeline perspective. Nat Prod Commun. 2011 Feb;6(2):287-300. [Content Brief]
