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Details

Stereochemistry RACEMIC
Molecular Formula C21H25NO4
Molecular Weight 355.4275
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TETRAHYDROPALMATINE, (±)-

SMILES

COC1=CC2=C(C=C1OC)C3CC4=C(CN3CC2)C(OC)=C(OC)C=C4

InChI

InChIKey=AEQDJSLRWYMAQI-UHFFFAOYSA-N
InChI=1S/C21H25NO4/c1-23-18-6-5-13-9-17-15-11-20(25-3)19(24-2)10-14(15)7-8-22(17)12-16(13)21(18)26-4/h5-6,10-11,17H,7-9,12H2,1-4H3

HIDE SMILES / InChI

Molecular Formula C21H25NO4
Molecular Weight 355.4275
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

DL-Tetrahydropalmatine (dl-THP), an active component isolated from Corydalis species (a Chinese herbal medicine). dl-THP has inhibitory effects on liver injury induced by carbon tetrachloride in mice. The drug demonstrated anxiolytic and anti-nociceptive effects in animal models. dl-THP may act through inhibition of amygdaloid dopamine release to inhibit an epileptic attack – it is a very effective anti-epileptogenic and anticonvulsant agent. dl-THP has been found to have antihypertensive effects. It acts through the 5-HT2 and/or D2-receptor antagonism in the hypothalamus to induce hypotension and bradycardia in rats.

Originator

Sources: DOI: 10.1039/JR9270000548

Approval Year

PubMed

PubMed

TitleDatePubMed
Antinociceptive effects of intragastric DL-tetrahydropalmatine on visceral and somatic persistent nociception and pain hypersensitivity in rats.
2011-11
[Difference absorption of l-tetrahydropalmatine and dl-tetrahydropalmatine in intestine of rats].
2007-05
A novel synthesis of tetrahydropalmatine.
1969-05-10
[RESEARCH ON THE COMPARATIVE PHARMACOLOGY OF PALMATINE AND DL-TETRAHYDROPALMATINE].
1965-03
SOME PHARMACOLOGICAL PROPERTIES OF CORYDALIS B (TETRAHYDROPALMATINE) AND ITS RELATED COMPOUNDS.
1964-04
[STUDIES ON THE PHARMACOLOGICAL ACTIONS OF CORYDALIS. XII. THE EFFECTS OF OPTICAL ISOMERS OF TETRAHYDROPALMATINE (THP) ON THE CENTRAL NERVOUS SYSTEM].
1964-03
Pharmacological study of tetrahydropalmatine and its analogs. A new type of central depressants.
1962-10-01
[On the pharmacology of rotundine].
1961-05-01
Patents

Patents

Sample Use Guides

Mice: 20, 40 mg/kg daily for 9 days
Route of Administration: Intraperitoneal
In an isolated perfused rat heart model, dl-tetrahydropalmatine (THP) at the concentration of 100 uM was found to have a negative effect (-45%) on left ventricular pressure and this effect was produced concentration-dependently from concentrations lower than 50 uM. In isolated cardiomyocytes, radioactive calcium influx was also inhibited significantly by THP at the concentration of 100 uM and this effect was also in a concentration-dependent manner (-39%).
Substance Class Chemical
Created
by admin
on Mon Mar 31 22:06:04 GMT 2025
Edited
by admin
on Mon Mar 31 22:06:04 GMT 2025
Record UNII
78F8583LNQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TETRAHYDROPALMATINE, (±)-
Common Name English
TETRAHYDROPALMATINE [MI]
Preferred Name English
TETRAHYDROPALMATINE, DL-
Common Name English
Code System Code Type Description
CAS
10097-84-4
Created by admin on Mon Mar 31 22:06:04 GMT 2025 , Edited by admin on Mon Mar 31 22:06:04 GMT 2025
SUPERSEDED
PUBCHEM
5417
Created by admin on Mon Mar 31 22:06:04 GMT 2025 , Edited by admin on Mon Mar 31 22:06:04 GMT 2025
PRIMARY
FDA UNII
78F8583LNQ
Created by admin on Mon Mar 31 22:06:04 GMT 2025 , Edited by admin on Mon Mar 31 22:06:04 GMT 2025
PRIMARY
EPA CompTox
DTXSID20864207
Created by admin on Mon Mar 31 22:06:04 GMT 2025 , Edited by admin on Mon Mar 31 22:06:04 GMT 2025
PRIMARY
MERCK INDEX
m10630
Created by admin on Mon Mar 31 22:06:04 GMT 2025 , Edited by admin on Mon Mar 31 22:06:04 GMT 2025
PRIMARY
CAS
2934-97-6
Created by admin on Mon Mar 31 22:06:04 GMT 2025 , Edited by admin on Mon Mar 31 22:06:04 GMT 2025
PRIMARY