Medical dictionary
Medical terminology normalized via MeSH, ICD-11, SNOMED CT.
62,341 terms indexed
from Alternanthera philoxeroides; structure in first source
from Thalictrum fortunei; structure in first source
from Thalictrum fortunei; structure in first source
from the husks of Xanthoceras sorbifolia Bunge; structure in first source
from Abrus precatorius Linn; structure in first source
- C5843373-O-beta-D-glucopyranosyl-(1-3)-beta-D-glucopyranosyl-(1-3)-beta-D-glucopyranosyl echinocystic acidMeSH
from the leaves of Aralia elata; structure in first source
from the leaves of Aralia elata; structure in first source
isolated from the rhizomes of Ardisia gigantifolia; structure in first source
from the husks of Xanthoceras sorbifolia Bunge; structure in first source
from the seeds of Hippophae rhamnoides subsp. sinensis; structure in first source
from the seeds of Hippophae rhamnoides subsp. sinensis; structure in first source
from the seeds of Hippophae rhamnoides subsp. sinensis; structure in first source
from the aerial parts of Lygodium japonicum; structure in first source
structure in first source
isolated from Swertia punicea; structure in first source
an antineoplastic agent isolated from Verbascum thapsus; structure in first source
enhances toxicity of saporin; isolated from Gypsophila arrostii; structure in first source
a ginsenoside Rh2 metabolite with antineoplastic activity; structure in first source
- C5707753-O-glucopyranosyloleanolic acid 28-O-xylopyranosyl-(1-4)-rhamnopyranosyl-(1-2)-xylopyranosideMeSH
has antineoplastic activity; isolated from Butyrospermum parkii; structure in first source
has anti-inflammatory activity; isolated from Sasa quelpaertensis
has antineoplastic activity; structure in first source
An enzyme that catalyzes the reduction of TESTOSTERONE to 5-ALPHA DIHYDROTESTOSTERONE.
A 3-oxoacyl reductase that has specificity for ACYL CARRIER PROTEIN-derived FATTY ACIDS.
An enzyme of long-chain fatty acid synthesis, that adds a two-carbon unit from malonyl-(acyl carrier protein) to another molecule of fatty acyl-(acyl carrier protein), giving a beta-ketoacyl-(acyl carrier protein) with the release of carbon dioxide. EC 2.3.1.41.
Highly conserved protein-serine threonine kinases that phosphorylate and activate a group of AGC protein kinases, especially in response to the production of the SECOND MESSENGERS, phosphatidylinositol 3,4,-biphosphate (PtdIns(3,4)P2) and phosphatidylinositol 3,4,5-triphosphate (PtdIns(3,4,5)P3).
An enzyme of the shikimate pathway of AROMATIC AMINO ACID biosynthesis, it generates 5-enolpyruvylshikimate 3-phosphate and ORTHOPHOSPHATE from PHOSPHOENOLPYRUVATE and shikimate-3-phosphate. The shikimate pathway is present in BACTERIA and PLANTS but not in MAMMALS.
A dihydropyridine derivative, which, in contrast to NIFEDIPINE, functions as a calcium channel agonist. The compound facilitates Ca2+ influx through partially activated voltage-dependent Ca2+ channels, thereby causing vasoconstrictor and positive inotropic effects. It is used primarily as a research tool.
anti-aphrodisiac male pheromone from Drosophila melanogaster; structure in first source
an antifungal agent isolated from Vitex negundo; structure in first source
has neuroprotective and antiparkinson activity; structure in first source
vitamin K1 2,3-epoxide reductase (VKOR) inhibitor that reduces experimental glomerulonephritis
structure in first source
inhibits 17beta-HSD1; structure in first source
structure in first source
has antineoplastic activity; structure in first source
from stem and leaf of Quercus variabilis; structure in first source
A 3-hydroxysteroid dehydrogenase which catalyzes the reversible reduction of the active androgen, DIHYDROTESTOSTERONE to 5 ALPHA-ANDROSTANE-3 ALPHA,17 BETA-DIOL. It also has activity towards other 3-alpha-hydroxysteroids and on 9-, 11- and 15- hydroxyprostaglandins. The enzyme is B-specific in reference to the orientation of reduced NAD or NADPH.
has antineoplastic activity; structure in first source
degradation product of aliskiren; structure in first source
structure in first source
an aminopeptidase inhibitor; structure in first source
structure in first source
structure in first source
structure in first source
structure in first source
a retinoid X receptor ligand; structure in first source
an antineoplastic activity; structure in first source
has antineoplastic activity; structure in first source
an antineoplastic agent; structure in first source