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Details

Stereochemistry ABSOLUTE
Molecular Formula C29H40O9
Molecular Weight 532.6225
Optical Activity UNSPECIFIED
Defined Stereocenters 13 / 13
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CALACTIN

SMILES

[H][C@@]12CC[C@]3([H])[C@]([H])(CC[C@]4(C)[C@H](CC[C@]34O)C5=CC(=O)OC5)[C@]1(C[C@@]6([H])O[C@@]7(O)[C@H](O)C[C@@H](C)O[C@@]7([H])O[C@]6([H])C2)C=O

InChI

InChIKey=OWPWFVVPBYFKBG-SXDHXEJRSA-N
InChI=1S/C29H40O9/c1-15-9-23(31)29(34)25(36-15)37-21-11-17-3-4-20-19(27(17,14-30)12-22(21)38-29)5-7-26(2)18(6-8-28(20,26)33)16-10-24(32)35-13-16/h10,14-15,17-23,25,31,33-34H,3-9,11-13H2,1-2H3/t15-,17+,18-,19+,20-,21-,22-,23-,25+,26-,27-,28+,29+/m1/s1

HIDE SMILES / InChI
Calactin and calotropin were the major cardenolides in Danaus plexippus reared on A. fruticosa or A. curassavica. It was discovered, that calactin could be potential anticancer compound that was supported for human leukemia cells. It was shown, that calactin decreased the expression of cell cycle regulatory proteins Cyclin B1, Cdk1, and Cdc25C was consistent with a G2/M phase arrest. Furthermore, calactin induced extracellular signal-regulated kinase (ERK) phosphorylation, activation of caspase-3, caspase-8, and caspase-9, and PARP cleavage.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
The growth inhibitory activity of the calactin was evaluated against human A549 and Hela cell lines. This compound showed the highest activity with IC50s values of (0.036 μM, A-549) and (0.083 μM, Hela)
Name Type Language
CALACTIN
Common Name English
PEKILOCERIN B
Common Name English
POEKILOCERIN B
Common Name English
PECILOCERIN B
Common Name English
CARD-20(22)-ENOLIDE, 14-HYDROXY-19-OXO-2,3-(((2S,3S,4R,6R)-TETRAHYDRO-3,4-DIHYDROXY-6-METHYL-2H-PYRAN-3,2-DIYL)BIS(OXY))-, (2.ALPHA.,3.BETA.,5.ALPHA.)-
Systematic Name English
POKILOCERIN B
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID80174192
Created by admin on Sat Dec 16 09:52:45 GMT 2023 , Edited by admin on Sat Dec 16 09:52:45 GMT 2023
PRIMARY
PUBCHEM
441849
Created by admin on Sat Dec 16 09:52:45 GMT 2023 , Edited by admin on Sat Dec 16 09:52:45 GMT 2023
PRIMARY
CAS
20304-47-6
Created by admin on Sat Dec 16 09:52:45 GMT 2023 , Edited by admin on Sat Dec 16 09:52:45 GMT 2023
PRIMARY
FDA UNII
6299V7SZXG
Created by admin on Sat Dec 16 09:52:45 GMT 2023 , Edited by admin on Sat Dec 16 09:52:45 GMT 2023
PRIMARY
HSDB
3467
Created by admin on Sat Dec 16 09:52:45 GMT 2023 , Edited by admin on Sat Dec 16 09:52:45 GMT 2023
PRIMARY