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Details

Stereochemistry ABSOLUTE
Molecular Formula C22H28N2O5.ClH
Molecular Weight 436.929
Optical Activity UNSPECIFIED
Defined Stereocenters 6 / 6
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RESERPIC ACID HYDROCHLORIDE

SMILES

Cl.CO[C@H]1[C@H](O)C[C@@H]2CN3CCC4=C(NC5=C4C=CC(OC)=C5)[C@H]3C[C@@H]2[C@@H]1C(O)=O

InChI

InChIKey=QLKKMNXYROCXRE-BCRILHLVSA-N
InChI=1S/C22H28N2O5.ClH/c1-28-12-3-4-13-14-5-6-24-10-11-7-18(25)21(29-2)19(22(26)27)15(11)9-17(24)20(14)23-16(13)8-12;/h3-4,8,11,15,17-19,21,23,25H,5-7,9-10H2,1-2H3,(H,26,27);1H/t11-,15+,17-,18-,19+,21+;/m1./s1

HIDE SMILES / InChI
Reserpic acid, a derivative of the antihypertensive drug reserpine, can inhibit norepinephrine uptake although it is much less effective than reserpine itself. Recently was shown, that reserpic acid possessed a strong binding to the pancreatic lipase, a major target for controlling the obesity.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P16233
Gene ID: 5406.0
Gene Symbol: PNLIP
Target Organism: Homo sapiens (Human)
Target ID: P23975
Gene ID: 6530.0
Gene Symbol: SLC6A2
Target Organism: Homo sapiens (Human)
4.5 µM [Ki]
Target ID: P23975
Gene ID: 6530.0
Gene Symbol: SLC6A2
Target Organism: Homo sapiens (Human)
4.5 µM [Ki]
Target ID: P16233
Gene ID: 5406.0
Gene Symbol: PNLIP
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
Medicinal plant phytochemicals and their inhibitory activities against pancreatic lipase: molecular docking combined with molecular dynamics simulation approach.
2018-05
Reserpic acid as an inhibitor of norepinephrine transport into chromaffin vesicle ghosts.
1985-09-15
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Reserpic acid inhibits norepinephrine uptake although it is much less effective than reserpine itself. A Lineweaver-Burk analysis indicated that reserpic acid was a competitive inhibitor of norepinephrine transport. In the experiments: Ghosts were suspended in 1.0 ml of 0.4 M sucrose, 40 mM Mes, pH 6.8 or 1.0 ml of 0.4 M sucrose, 40 mM Hepes, pH 7.8, containing 5 mM ATP, 5 mM MgSO4, and concentration of inhibitor (reserpic acid): 3-300 uM. Chromaffin vesicles were prepared from the bovine adrenal medulla. Ghosts were prepared by resuspending the vesicles in the lysis medium.
Name Type Language
NSC-118178
Preferred Name English
RESERPIC ACID HYDROCHLORIDE
Common Name English
YOHIMBAN-16-CARBOXYLIC ACID, 18-HYDROXY-11,17-DIMETHOXY-, HYDROCHLORIDE (1:1), (3.BETA.,16.BETA.,17.ALPHA.,18.BETA.,20.ALPHA.)-
Common Name English
RESERPIC ACID, MONOHYDROCHLORIDE
Common Name English
Code System Code Type Description
PUBCHEM
17751039
Created by admin on Mon Mar 31 23:02:48 GMT 2025 , Edited by admin on Mon Mar 31 23:02:48 GMT 2025
PRIMARY
EPA CompTox
DTXSID80637974
Created by admin on Mon Mar 31 23:02:48 GMT 2025 , Edited by admin on Mon Mar 31 23:02:48 GMT 2025
PRIMARY
FDA UNII
YK1DUA2LXK
Created by admin on Mon Mar 31 23:02:48 GMT 2025 , Edited by admin on Mon Mar 31 23:02:48 GMT 2025
PRIMARY
NSC
118178
Created by admin on Mon Mar 31 23:02:48 GMT 2025 , Edited by admin on Mon Mar 31 23:02:48 GMT 2025
PRIMARY
CAS
1910-70-9
Created by admin on Mon Mar 31 23:02:48 GMT 2025 , Edited by admin on Mon Mar 31 23:02:48 GMT 2025
PRIMARY