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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 CALOTROPIN

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-NYVHBPEFSA-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

Description
Curator's Comment: description was created based on several sources, including: http://www.avpayurveda.com/dmdocuments/AMJ%2090.10.pdf | https://www.ncbi.nlm.nih.gov/pubmed/27498029 | https://www.ncbi.nlm.nih.gov/pubmed/14224519

Calotropin is an pharmacologically active compound isolated from Asclepias curasavica L. Whereas calotropin possesses cytotoxicity against several cancer cells, the mechanisms of action remain unclear. Calotropin inhibits the Wnt signaling pathway by increasing CK1α protein levels.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
CALOTROPIN, A CYTOTOXIC PRINCIPLE ISOLATED FROM ASCLEPIAS CURASSAVICA L.
1964 Dec 25
Calotropin from Asclepias curasavica induces cell cycle arrest and apoptosis in cisplatin-resistant lung cancer cells.
2016 Sep 16
Patents

Sample Use Guides

Calotropin was administered through gavage 25 mg/kg body wt. each day for a period of 30 days to male gerbils and rabbits
Route of Administration: Oral
The inhibitory effects of Calotropin on the viability of A549 and A549/ CDDP cells were determined by MTT assay. A549/CDDP cells were significantly inhibited by Calotropin in a concentration-dependent manner with an IC50 of 0.33 ± 0.06 uM at 48 h.
Name Type Language
CALOTROPIN
MI  
Common Name English
CARD-20(22)-ENOLIDE, 14-HYDROXY-19-OXO-2,3-(((2S,3S,4S,6R)-TETRAHYDRO-3,4-DIHYDROXY-6-METHYL-2H-PYRAN-3,2-DIYL)BIS(OXY))-, (2.ALPHA.,3.BETA.,5.ALPHA.)-
Systematic Name English
(2.ALPHA.,3.BETA.,5.ALPHA.)-14-HYDROXY-19-OXO-2,3-(((2S,3S,4S,6R)-TETRAHYDRO-3,4-DIHYDROXY-6-METHYL-2H-PYRAN-3,2-DIYL)BIS(OXY))CARD-20(22)-ENOLIDE
Systematic Name English
CALOTROPIN [MI]
Common Name English
NSC-143925
Code English
PECILOCERIN A
Common Name English
PEKILOCERIN A
Common Name English
Code System Code Type Description
HSDB
3470
Created by admin on Sat Dec 16 09:04:19 GMT 2023 , Edited by admin on Sat Dec 16 09:04:19 GMT 2023
PRIMARY
MERCK INDEX
m2992
Created by admin on Sat Dec 16 09:04:19 GMT 2023 , Edited by admin on Sat Dec 16 09:04:19 GMT 2023
PRIMARY Merck Index
CAS
1986-70-5
Created by admin on Sat Dec 16 09:04:19 GMT 2023 , Edited by admin on Sat Dec 16 09:04:19 GMT 2023
PRIMARY
PUBCHEM
16142
Created by admin on Sat Dec 16 09:04:19 GMT 2023 , Edited by admin on Sat Dec 16 09:04:19 GMT 2023
PRIMARY
EPA CompTox
DTXSID10173613
Created by admin on Sat Dec 16 09:04:19 GMT 2023 , Edited by admin on Sat Dec 16 09:04:19 GMT 2023
PRIMARY
WIKIPEDIA
Calotropin
Created by admin on Sat Dec 16 09:04:19 GMT 2023 , Edited by admin on Sat Dec 16 09:04:19 GMT 2023
PRIMARY
FDA UNII
3XK21U1BZS
Created by admin on Sat Dec 16 09:04:19 GMT 2023 , Edited by admin on Sat Dec 16 09:04:19 GMT 2023
PRIMARY
NSC
143925
Created by admin on Sat Dec 16 09:04:19 GMT 2023 , Edited by admin on Sat Dec 16 09:04:19 GMT 2023
PRIMARY