Compound Summary
Compound Name: | cantharidic acid |
Compound CID: | 2544 |
Synonyms: | cantharidic acid NSC115503 2,3-dimethyl-7-oxabicyclo2.2.1heptane-2,3-dicarboxylic acid Lopac0_000318 SCHEMBL943636 More... |
Iupac Name: | 2,3-dimethyl-7-oxabicyclo[2.2.1]heptane-2,3-dicarboxylic acid |
InChI: | InChI=1S/C10H14O5/c1-9(7(11)12)5-3-4-6(15-5)10(9,2)8(13)14/h5-6H,3-4H2,1-2H3,(H,11,12)(H,13,14) |
InChIKey: | NMTNUQBORQILRK-UHFFFAOYSA-N |
Canonical Smiles: | CC1(C2CCC(C1(C)C(=O)O)O2)C(=O)O |
Isomeric Smiles: | CC1(C2CCC(C1(C)C(=O)O)O2)C(=O)O |
Molecular Weight: | 214.21 |
Molecular Formula: | C10H14O5 |
Molecular Weight: | 214.21 |
Molecular Formula: | C10H14O5 |
Hydrogen Bond Donor Count: | 2 |
Hydrogen Bond Acceptor Count: | 5 |
Rotatable Bond Count: | 2 |
Heavy Atom Count: | 15 |
Complexity: | 307 |
cantharidic acid | cantharidic acid |
---|---|
cantharidic acid |
NSC115503 |
2,3-dimethyl-7-oxabicyclo2.2.1heptane-2,3-dicarboxylic acid |
Lopac0_000318 |
SCHEMBL943636 |
BMK1-G11 |
CHEMBL275516 |
HMS3260P18 |
exo-1,6-Dicarboxy-endo-1,6-dimethyl-7-oxabicylco2,2,1heptane |
Tox21_500318 |
5′-3′2,3-Dicarboxy-2,3-dimethyl-1,4-epoxycyclohexane |
HSCI1_000263 |
CCG-204413 |
LP00318 |
NSC-115503 |
SDCCGSBI-0050306.P002 |
NCGC00015272-02 |
NCGC00015272-03 |
NCGC00015272-04 |
NCGC00015272-05 |
NCGC00093763-01 |
NCGC00093763-02 |
NCGC00261003-01 |
EU-0100318 |
C 8088 |
SR-01000075783 |
SR-01000075783-1 |
exo-2,3-di-methyl-7-oxabicyclo2.2.1heptane-2,3-dicarboxylic acid |
Species | Dose | Unit | Control(Avg days) | Treatment(Avg days) | Avg/Med Lifespan Change(%) | Control(Max days) | Treatment(Max days) | Max Lifespan Change(%) | Significant | Strain | Gender | PubMed | Avg/Med Lifespan Change tab |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Caenorhabditis elegans | 33.000000000000000 | umol/L | -29.000000000000000 | NS | N2 | 24134630 | Inactive |
Species | Avg/Med Lifespan Change(%) | Max Lifespan Change(%) | Count Reference | Count Data point |
---|---|---|---|---|
Caenorhabditis elegans | -29.000000000000000 | 1 | 1 |