
CAS 21302-79-4: Ceanothic acid
Formula:C30H46O5
InChI:InChI=1S/C30H46O5/c1-16(2)17-10-13-30(25(34)35)15-14-27(5)18(21(17)30)8-9-20-28(27,6)12-11-19-26(3,4)23(31)22(24(32)33)29(19,20)7/h17-23,31H,1,8-15H2,2-7H3,(H,32,33)(H,34,35)/t17-,18+,19-,20-,21+,22+,23-,27+,28+,29-,30-/m0/s1
InChI key:InChIKey=WLCHQSHZHFLMJH-VILVJDKQSA-N
SMILES:C[C@@]12[C@@]3([C@](C)([C@@]4(C)[C@](CC3)([C@@]5([C@@](C(O)=O)(CC4)CC[C@H]5C(C)=C)[H])[H])CC[C@]1(C(C)(C)[C@@H](O)[C@@H]2C(O)=O)[H])[H]
Synonyms:- (2a,3b)-3-Hydroxy-A(1),28-dinorlup-20(29)-ene-2,17-dicarboxylic acid
- (3β,3′β,4α,4′α,5β,8α,9β,10α,13α,14β,15β)-Tetrahydro-4′-hydroxy-4,5′,5′,9-tetramethyl-15-(1-methylethenyl)-3′H-cyclopenta[3,4]-18-norandrost-3-ene-3′,13-dicarboxylic acid
- 21302-79-4
- 2α-Carboxy-3β-hydroxy-A(1)-norlup-20(29)-en-28-oic acid
- 3′H-Cyclopenta[3,4]-18-norandrost-3-ene-3′,13-dicarboxylic acid, tetrahydro-4′-hydroxy-4,5′,5′,9-tetramethyl-15-(1-methylethenyl)-, (3β,3′β,4α,4′α,5β,8α,9β,10α,13α,14β,15β)-
- A(1),28-Dinorlup-20(29)-ene-2,17-dicarboxylic acid, 3-hydroxy-, (2α,3β)-
- A(1)-Norlup-20(29)-en-28-oic acid, 2α-carboxy-3β-hydroxy-
- Ceanothic acid
- Emmolic Acid
- dicyclopenta[a,i]phenanthrene-1,7a(1H)-dicarboxylic acid, octadecahydro-2-hydroxy-3,3,5a,5b,12b-pentamethyl-10-(1-methylethenyl)-, (1R,2S,3aR,5aR,5bR,7aS,10R,10aR,10bR,12aR,12bR)-
- (1R,2S,3aR,5aR,5bR,7aS,10R,10aR,10bR,12aR,12bR)-2-Hydroxy-3,3,5a,5b,12b-pentamethyl-10-(prop-1-en-2-yl)octadecahydrodicyclopenta[a,i]phenanthrene-1,7a(1H)-dicarboxylic acid
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Ceanothic acid
CAS:Ceanothic acid is a triterpenoid compound, which is a type of natural organic molecule found predominantly in various species of the Rhamnaceae family. This compound is typically extracted from the root bark of Ceanothus plants, commonly known as red-root or New Jersey tea. The mode of action of ceanothic acid involves modulation of biochemical pathways associated with inflammation and cancer cell proliferation. It achieves its effects by interacting with specific enzymatic and receptor targets, thereby influencing cellular signaling pathways. Ceanothic acid is utilized in scientific research for its potential applications in developing therapeutic agents, particularly in areas targeting inflammatory diseases and certain types of cancer. Its role in modulating immune responses has implications for treating conditions like arthritis and autoimmune disorders. Additionally, its antiproliferative effects make it a candidate for cancer research, where it is studied as a potential adjuvant in chemotherapy. The exploration of ceanothic acid continues to be a significant area of interest, aiming to elucidate its mechanisms and expand its applicability in medical science.Formula:C30H46O5Purity:Min. 95%Molecular weight:486.7 g/molCeanothic acid
CAS:Ceanothic acid derivatives show cytotoxic effect against OVCAR-3 and HeLa cancer cell lines.Formula:C30H46O5Purity:98%Color and Shape:SolidMolecular weight:486.693