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Home Other Building Blocks 4339-72-4
4339-72-4,MFCD09752429
Catalog No.:AA00DGUR

4339-72-4 | 3-O-Acetyloleanolic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1mg
≥95%
in stock  
$133.00   $93.00
- +
5mg
≥95%
in stock  
$490.00   $343.00
- +
10mg
≥95%
in stock  
$718.00   $502.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00DGUR
Chemical Name:
3-O-Acetyloleanolic acid
CAS Number:
4339-72-4
Molecular Formula:
C32H50O4
Molecular Weight:
498.7370
MDL Number:
MFCD09752429
SMILES:
CC(=O)O[C@H]1CC[C@]2([C@H](C1(C)C)CC[C@@]1([C@@H]2CC=C2[C@@]1(C)CC[C@@]1([C@H]2CC(C)(C)CC1)C(=O)O)C)C
Properties

Upstream Synthesis Route

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[52]Chem.Abstr.,1934,p.1998

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[54]JournaloftheChemicalSociety,1939,p.1045,1047

[55]HelveticaChimicaActa,1936,vol.19,p.1136

[56]HelveticaChimicaActa,1937,vol.20,p.229Anm.3

[57]YakugakuZasshi,1930,vol.50,p.1076,1086;dtsch.Ref.S.139

[58]Chem.Zentralbl.,1931,vol.102,#I,p.1118

[59]ScientificPapersoftheInstituteofPhysicalandChemicalResearch(Japan),1932,vol.18,p.83,95

[60]YakugakuZasshi,1933,vol.53,p.680,685;dtsch.Ref.S.129

[61]Chem.Abstr.,1934,p.1998

[62]YakugakuZasshi,1947,vol.67,p.206

[63]Chem.Abstr.,1951,p.9069

[64]YakugakuZasshi,1933,vol.53,p.680,685;dtsch.Ref.S.129

[65]Chem.Abstr.,1934,p.1998

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[69]YakugakuZasshi,1933,vol.53,p.680,685;dtsch.Ref.S.129

[70]Chem.Abstr.,1934,p.1998

[71]HelveticaChimicaActa,1936,vol.19,p.1136

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[1]EuropeanJournalofMedicinalChemistry,2014,vol.87,p.316-327

[2]YakugakuZasshi,1933,vol.53,p.680,685;dtsch.Ref.S.129

[3]Chem.Abstr.,1934,p.1998

[4]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1931,vol.199,p.56,62

[5]ScientificPapersoftheInstituteofPhysicalandChemicalResearch(Japan),1932,vol.18,p.83,95

[6]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1931,vol.199,p.56,62

[7]YakugakuZasshi,1947,vol.67,p.206

[8]Chem.Abstr.,1951,p.9069

[9]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1931,vol.199,p.56,62

[10]JournalofBiologicalChemistry,1938,vol.123,p.641,651,652

[11]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1931,vol.199,p.56,62

[12]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1931,vol.195,p.132

[13]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1931,vol.198,p.182

[14]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1931,vol.199,p.64,66,71

[15]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1932,vol.211,p.5,16

[16]Hoppe-Seyler'sZeitschriftfuerPhysiologischeChemie,1931,vol.199,p.56,62

[17]JournaloftheChemicalSociety,1939,p.1045,1047

[18]HelveticaChimicaActa,1936,vol.19,p.1136

[19]HelveticaChimicaActa,1937,vol.20,p.229Anm.3

[20]YakugakuZasshi,1930,vol.50,p.1076,1086;dtsch.Ref.S.139

[21]Chem.Zentralbl.,1931,vol.102,#I,p.1118

[1]EuropeanJournalofMedicinalChemistry,2018,vol.152,p.21-30

[2]ScientificPapersoftheInstituteofPhysicalandChemicalResearch(Japan),1932,vol.18,p.83,95

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[7]YakugakuZasshi,1930,vol.50,p.1076,1086;dtsch.Ref.S.139

[8]Chem.Zentralbl.,1931,vol.102,#I,p.1118

[1]Molecules,2011,vol.16,#6,p.4748-4763

[1]JournaloftheChemicalSociety,1908,vol.93,p.903,916

[2]BerichtederDeutschenPharmazeutischenGesellschaft,vol.15,p.121

[3]Chem.Zentralbl.,1905,vol.76,#II,p.553

[4]MonatsheftefuerChemie,1905,vol.26,p.387

[5]JournaloftheAmericanChemicalSociety,1918,vol.40,p.1919

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[8]RecueildesTravauxChimiquesdesPays-Bas,1929,vol.48,p.611

[9]RecueildesTravauxChimiquesdesPays-Bas,1929,vol.48,p.609

[10]JournaloftheChemicalSociety,1908,vol.93,p.903,916

[11]BerichtederDeutschenPharmazeutischenGesellschaft,vol.15,p.121

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[13]MonatsheftefuerChemie,1905,vol.26,p.387

[14]JournaloftheAmericanChemicalSociety,1918,vol.40,p.1919

[15]JournaloftheAmericanChemicalSociety,1930,vol.52,p.1722

[16]RecueildesTravauxChimiquesdesPays-Bas,1927,vol.46,p.788,790

[17]RecueildesTravauxChimiquesdesPays-Bas,1929,vol.48,p.611

[18]RecueildesTravauxChimiquesdesPays-Bas,1929,vol.48,p.609

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[20]JournaloftheAmericanChemicalSociety,1918,vol.40,p.1919

[21]JournaloftheAmericanChemicalSociety,1930,vol.52,p.1722

Downstream Synthesis Route

[1]JournalofMedicinalChemistry,2016,vol.59,p.2396-2409

[2]JournalofMedicinalChemistry,2016,vol.59,p.2396-2409

[1]JournalofMedicinalChemistry,2016,vol.59,p.2396-2409

[2]JournalofMedicinalChemistry,2016,vol.59,p.2396-2409

3048-01-9    4339-72-4   
N-(o-trifluoromethylbenzyl)-(3β)-acetyloxy-olean-12-en-28-amide 

[1]Heller,Lucie;Knorrscheidt,Anja;Flemming,Franziska;Wiemann,Jana;Sommerwerk,Sven;Pavel,IoanaZ.;Al-Harrasi,Ahmed;Csuk,René[BioorganicChemistry,2016,vol.68,p.137-151]

27578-60-5    4339-72-4   
(3β)-N-(2-piperidin-1-ylethyl)-3-acetyloxy-olean-12-en-28-amide 

[1]Molecules,2019,vol.24

[2]Steroids,2019,vol.149

646-24-2    4339-72-4   
1ccc 

[1]Steroids,2019,vol.149

Literature

Title: Yoo KH, et al. 3-O-acetyloleanolic acid induces apoptosis in human colon carcinoma HCT-116 cells. Phytother Res. 2012 Oct;26(10):1541-6.

Title: Hwang-Bo J, et al. 3-O-Acetyloleanolic acid inhibits VEGF-A-induced lymphangiogenesis and lymph node metastasis in an oral cancer sentinel lymph node animal model. BMC Cancer. 2018 Jul 5;18(1):714.

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