Morolic acid

Modify Date: 2026-07-15 12:19:54

Morolic acid Structure
Morolic acid structure
Common Name Morolic acid
CAS Number 559-68-2 Molecular Weight 456.70000
Density N/A Boiling Point N/A
Molecular Formula C30H48O3 Melting Point N/A
MSDS N/A Flash Point N/A

 Use of Morolic acid


Morolic acid (compound 6) can be isolated from Phoradendron brachystachyum DC Nutt. Morolic acid has antiretroviral activity[1].

 Names

Name Morolsaeure
Synonym More Synonyms

 Morolic acid Biological Activity

Description Morolic acid (compound 6) can be isolated from Phoradendron brachystachyum DC Nutt. Morolic acid has antiretroviral activity[1].
Related Catalog
References

[1]. Sugey López-Martínez, et al. Chemical constituents of the hemiparasitic plant Phoradendron brachystachyum DC Nutt (Viscaceae). Formerly Natural Product Letters. 2013, 27.

 Chemical & Physical Properties

Molecular Formula C30H48O3
Molecular Weight 456.70000
Exact Mass 456.36000
PSA 57.53000
LogP 7.23360
InChIKey RGZSSKBTFGNUCG-VNTGHVHSSA-N
SMILES CC1(C)C=C2C3CCC4C5(C)CCC(O)C(C)(C)C5CCC4(C)C3(C)CCC2(C(=O)O)CC1

 Morolic acidBioassay

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Name: Antidiabetic activity in STZ-nicotinamide diabetic Wistar rat T2DM model assessed as ...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL2149252
Name: Antidiabetic activity in STZ-nicotinamide diabetic Wistar rat T2DM model assessed as ...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL2149253
Name: Antidiabetic activity in STZ-nicotinamide diabetic Wistar rat T2DM model assessed as ...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL2149251
Name: Inhibition of human recombinant PTP-1B expressed in Escherichia coli TB1 using p-nitr...
Source: ChEMBL
Target: Tyrosine-protein phosphatase non-receptor type 1
External Id: CHEMBL2149371
Name: Inhibition of human recombinant PTP-1B expressed in Escherichia coli TB1 using p-nitr...
Source: ChEMBL
Target: Tyrosine-protein phosphatase non-receptor type 1
External Id: CHEMBL2149372
Name: Antidiabetic activity in STZ-nicotinamide diabetic Wistar rat T2DM model assessed as ...
Source: ChEMBL
Target: Rattus norvegicus
External Id: CHEMBL2149254
Name: Antiviral activity against HIV1 3B infected in human H9 cells assessed as inhibition ...
Source: ChEMBL
Target: Human immunodeficiency virus 1
External Id: CHEMBL949642
Name: Cytotoxicity against human H9 cells
Source: ChEMBL
Target: H9
External Id: CHEMBL949641
Name: HIV Cellular Data
Source: NIAID
Target: N/A
External Id: HIV Cellular Data
Name: Therapeutic index, ratio of IC50 for human H9 cells to EC50 of HIV1 3B
Source: ChEMBL
Target: N/A
External Id: CHEMBL949643
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 Synonyms

(6aR,6bR,8aR,10S,12aR,12bR,14aS)-10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3,4,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14,14a-octadecahydro-2H-picene-4a-carboxylic acid
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