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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H24N2O4
Molecular Weight 368.4263
Optical Activity UNSPECIFIED
Defined Stereocenters 5 / 5
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of UNCARINE A

SMILES

[H][C@@]12C[C@]3([H])C(=CO[C@H](C)[C@@]3([H])CN1CC[C@@]24C(=O)NC5=C4C=CC=C5)C(=O)OC

InChI

InChIKey=JMIAZDVHNCCPDM-DQDWJNSRSA-N
InChI=1S/C21H24N2O4/c1-12-14-10-23-8-7-21(16-5-3-4-6-17(16)22-20(21)25)18(23)9-13(14)15(11-27-12)19(24)26-2/h3-6,11-14,18H,7-10H2,1-2H3,(H,22,25)/t12-,13+,14-,18+,21+/m1/s1

HIDE SMILES / InChI
The stem, wood and bark of Uncaria kawakamii contain the two isomeric alkaloids, Uncarine A and Uncarine B, the highest proportion of alkaloids (1.48%) occurring in the bark. Uncarine A caused a marked decrease of systolic and diastolic pressures in renal or spontaneously hypertensive conscious rats, but not in normotensive rats. During the period of hypotensive action, the heart rate was increased. No effect on the noradrenaline content of the heart or on the pressor responses to noradrenaline, angiotensin II, or sympathetic stimulation was observed. The concentrations of plasma noradrenaline and adrenaline in the spontaneously hypertensive rat were markedly increased when the blood pressure was lowered. Uncarine A apparently reduces the blood pressure of hypertensive rats by a mechanism different from that of currently used antihypertensive agents. The site of action could be the central nervous system.

Originator

Sources: DOI: 10.1248/cpb.6.300

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Studies on uncaria alkaloid. XVIII. Structure of uncarine. 13. Structure of uncarine-A and uncarine-B.
1958 Jun
Isolation of isopteropodine from the marine mollusk Nerita albicilla: establishment of the structure via two dimensional NMR techniques.
1986 May-Jun
Patents

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Name Type Language
UNCARINE A
Common Name English
UNCARIN A
Common Name English
FORMOSANAN-16-CARBOXYLIC ACID, 19-METHYL-2-OXO-, METHYL ESTER, (7.ALPHA.,19.BETA.)-
Common Name English
SPIRO(3H-INDOLE-3,6'(4'AH)-(1H)PYRANO(3,4-F)INDOLIZINE)-4'-CARBOXYLIC ACID, 1,2,5',5'A,7',8',10',10'A-OCTAHYDRO-1'-METHYL-2-OXO-, METHYL ESTER, (1'R,3S,4'AS,5'AS,10'AR)-
Systematic Name English
ISOFORMOSANINE
Common Name English
7-ISOFORMOSANINE
Common Name English
Code System Code Type Description
CAS
6899-73-6
Created by admin on Sat Dec 16 18:11:35 GMT 2023 , Edited by admin on Sat Dec 16 18:11:35 GMT 2023
PRIMARY
PUBCHEM
188999
Created by admin on Sat Dec 16 18:11:35 GMT 2023 , Edited by admin on Sat Dec 16 18:11:35 GMT 2023
PRIMARY
FDA UNII
N27X6B2Q57
Created by admin on Sat Dec 16 18:11:35 GMT 2023 , Edited by admin on Sat Dec 16 18:11:35 GMT 2023
PRIMARY
EPA CompTox
DTXSID70110006
Created by admin on Sat Dec 16 18:11:35 GMT 2023 , Edited by admin on Sat Dec 16 18:11:35 GMT 2023
PRIMARY