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Details

Stereochemistry ABSOLUTE
Molecular Formula C24H40N2.2BrH
Molecular Weight 518.412
Optical Activity UNSPECIFIED
Defined Stereocenters 8 / 8
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CONESSINE HYDROBROMIDE

SMILES

Br.Br.C[C@H]1[C@H]2CC[C@H]3[C@@H]4CC=C5C[C@H](CC[C@]5(C)[C@H]4CC[C@]23CN1C)N(C)C

InChI

InChIKey=YYTFAPMEQOGSRL-VEOCRSHVSA-N
InChI=1S/C24H40N2.2BrH/c1-16-20-8-9-22-19-7-6-17-14-18(25(3)4)10-12-23(17,2)21(19)11-13-24(20,22)15-26(16)5;;/h6,16,18-22H,7-15H2,1-5H3;2*1H/t16-,18-,19+,20+,21-,22-,23-,24-;;/m0../s1

HIDE SMILES / InChI

Molecular Formula BrH
Molecular Weight 80.912
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C24H40N2
Molecular Weight 356.5878
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 8 / 8
E/Z Centers 0
Optical Activity UNSPECIFIED

Conessine is a plant steroid alkaloid that acts as a potent and specific antagonist of histamine H3 receptors. Conessine displayed high affinity at both rat and human H3 receptors (pKi = 7.61 and 8.27) and generally high selectivity against other sites, including histamine receptors H1, H2, and H4. Conessine was found to efficiently penetrate the CNS and reach very high brain concentrations. Although the very slow CNS clearance and strong binding to adrenergic receptors discouraged focus on conessine itself for further development, its potency and novel steroid-based skeleton motivated further chemical investigation. Modification based on introducing diversity at the 3-nitrogen position generated a new series of H3 antagonists with higher in vitro potency, improved target selectivity, and more favorable drug-like properties. Conessine also has high affinity for the adrenergic receptors. Conessine has being shown to possess anti-malarial activity. In India conessine finds therapeutic use for treatment of dysentery and helminthic disorders.

CNS Activity

Curator's Comment: Conessine was found to efficiently penetrate the CNS and reach very high brain concentrations. Conessine has sedative, central nervous system depressant activities.

Approval Year

PubMed

PubMed

TitleDatePubMed
International Union of Basic and Clinical Pharmacology. XCVIII. Histamine Receptors.
2015-07
Acute cardiac toxicity of nerium oleander/indicum poisoning (kaner) poisoning.
2010-10
The alkaloid conessine and analogues as potent histamine H3 receptor antagonists.
2008-09-11
Novel H3 receptor antagonists with improved pharmacokinetic profiles.
2008-07-15
Antagonist affinity measurements at the Gi-coupled human histamine H3 receptor expressed in CHO cells.
2008-06-06
Development and validation of a visible absorption densitometry method for quantitation of conessine in Holarrhena antidysenterica (Kurchi).
2008-05-15
A new family of H3 receptor antagonists based on the natural product Conessine.
2008-02-15
High-performance thin layer chromatography method for estimation of conessine in herbal extract and pharmaceutical dosage formulations.
2008-01-22
Chromatographic analysis of Kutajarista--an ayurvedic polyherbal formulation.
2008-01-17
Steroidal alkaloids from Holarrhena antidysenterica (L.) WALL.
2007-06
A new family of histamine H3 receptor antagonists based on a natural product: discovery, SAR, and properties of the series.
2007-04
Antibacterial activities of the extracts and conessine from Holarrhena floribunda G. Don. (Apocynaceae).
2007-02-16
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Isolation, characterization and antiplasmodial activity of steroidal alkaloids from Funtumia elastica (Preuss) Stapf.
2005-05-16
Highly enantioselective construction of fused pyrrolidine systems that contain a quaternary stereocenter: concise formal synthesis of (+)-conessine.
2004-05-03
Steroid hormone activity of flavonoids and related compounds.
2000-07
Déjà vu guides the way to new antimicrobial steroid.
1993-02-19
Squalamine: an aminosterol antibiotic from the shark.
1993-02-15
Patents

Patents

Sample Use Guides

Mice: Conessine significantly reduced parasitaemia (at 10 mg/kg exhibited 88.95% parasite inhibition) in P. berghei-infected mice. Conessine was administered orally to mice of different groups for four days
Route of Administration: Oral
Conessine showed in vitro anti-plasmodial activity with its IC₅₀ value 1.9 ug/ml and 1.3 ug/ml using schizont maturation and pLDH assay respectively. The compound showed cytotoxity IC₅₀= 14 ug/ml against L6 cells of rat skeletal muscle myoblast.
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:50:38 GMT 2025
Edited
by admin
on Mon Mar 31 18:50:38 GMT 2025
Record UNII
N9EQE108I5
Record Status Validated (UNII)
Record Version
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Name Type Language
CONESSINE HYDROBROMIDE
Common Name English
CONESSINE DIHYDROBROMIDE
MI  
Preferred Name English
CONESSINE DIHYDROBROMIDE [MI]
Common Name English
CON-5-ENIN-3-AMINE, N,N-DIMETHYL-, DIHYDROBROMIDE, (3.BETA.)-
Systematic Name English
CONESSINE HBR
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C221
Created by admin on Mon Mar 31 18:50:38 GMT 2025 , Edited by admin on Mon Mar 31 18:50:38 GMT 2025
Code System Code Type Description
EPA CompTox
DTXSID30974568
Created by admin on Mon Mar 31 18:50:38 GMT 2025 , Edited by admin on Mon Mar 31 18:50:38 GMT 2025
PRIMARY
PUBCHEM
111109
Created by admin on Mon Mar 31 18:50:38 GMT 2025 , Edited by admin on Mon Mar 31 18:50:38 GMT 2025
PRIMARY
ChEMBL
CHEMBL191703
Created by admin on Mon Mar 31 18:50:38 GMT 2025 , Edited by admin on Mon Mar 31 18:50:38 GMT 2025
PRIMARY
NCI_THESAURUS
C79872
Created by admin on Mon Mar 31 18:50:38 GMT 2025 , Edited by admin on Mon Mar 31 18:50:38 GMT 2025
PRIMARY
CAS
5913-82-6
Created by admin on Mon Mar 31 18:50:38 GMT 2025 , Edited by admin on Mon Mar 31 18:50:38 GMT 2025
PRIMARY
FDA UNII
N9EQE108I5
Created by admin on Mon Mar 31 18:50:38 GMT 2025 , Edited by admin on Mon Mar 31 18:50:38 GMT 2025
PRIMARY
MERCK INDEX
m3750
Created by admin on Mon Mar 31 18:50:38 GMT 2025 , Edited by admin on Mon Mar 31 18:50:38 GMT 2025
PRIMARY Merck Index
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ACTIVE MOIETY