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10376-50-8,MFCD04972177
Catalog No.:AA01CBBS

10376-50-8 | Lup-20(29)-en-28-oic acid, 3-(acetyloxy)-, (3b)-

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  • Technical Information
  • Properties
  • Literature
Technical Information
Catalog Number:
AA01CBBS
Chemical Name:
Lup-20(29)-en-28-oic acid, 3-(acetyloxy)-, (3b)-
CAS Number:
10376-50-8
Molecular Formula:
C32H50O4
Molecular Weight:
498.7370
MDL Number:
MFCD04972177
SMILES:
CC(=O)O[C@H]1CC[C@]2([C@H](C1(C)C)CC[C@@]1([C@@H]2CC[C@H]2[C@@]1(C)CC[C@@]1([C@@H]2[C@@H](CC1)C(=C)C)C(=O)O)C)C
Properties
Computed Properties
 
Complexity:
967  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
10  
Heavy Atom Count:
36  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
4  
XLogP3:
8.8  

Literature

Title: Hypericum lanceolatum (Hypericaceae) as a potential source of new anti-malarial agents: a bioassay-guided fractionation of the stem bark.

Journal: Malaria journal 20110101

Title: Small structural changes of pentacyclic lupane type triterpenoid derivatives lead to significant differences in their anticancer properties.

Journal: European journal of medicinal chemistry 20100801

Title: Antiprotozoal activity of betulinic acid derivatives.

Journal: Phytomedicine : international journal of phytotherapy and phytopharmacology 20100401

Title: Antimalarial activity of betulinic acid and derivatives in vitro against Plasmodium falciparum and in vivo in P. berghei-infected mice.

Journal: Parasitology research 20090701

Title: Synthesis and structure-activity relationship study of cytotoxic germanicane- and lupane-type 3beta-O-monodesmosidic saponins starting from betulin.

Journal: Bioorganic & medicinal chemistry 20070915

Title: Synthesis of A-seco derivatives of betulinic acid with cytotoxic activity.

Journal: Journal of natural products 20040701

Title: Development of C-20 modified betulinic acid derivatives as antitumor agents.

Journal: Bioorganic & medicinal chemistry letters 20010903

Title: Anti-AIDS agents, 11. Betulinic acid and platanic acid as anti-HIV principles from Syzigium claviflorum, and the anti-HIV activity of structurally related triterpenoids.

Journal: Journal of natural products 19940201

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Tags:10376-50-8 Molecular Formula|10376-50-8 MDL|10376-50-8 SMILES|10376-50-8 Lup-20(29)-en-28-oic acid, 3-(acetyloxy)-, (3b)-