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Class of enzymes
Thiamine kinase (EC 2.7.1.89) is an enzyme that catalyzes the chemical reaction ATP + thiamine ADP + thiamine monophosphate The enzyme
Thiamine_kinase
Chemical compound and essential nutrient
Thiamine, also known as thiamin and vitamin B1, is a vitamin – an essential micronutrient for humans and animals. It is found in food and commercially
Thiamine
Class of enzymes
Thiamine-phosphate kinase (EC 2.7.4.16) is an enzyme that catalyzes the chemical reaction thiamine monophosphate ATP ADP ATP ADP thiamine pyrophosphate
Thiamine-phosphate_kinase
Class of enzymes
Thiamine-diphosphate kinase is an enzyme involved in thiamine metabolism. It catalyzes the chemical reaction thiamine pyrophosphate ATP ADP ATP ADP
Thiamine-diphosphate_kinase
Class of enzymes
accession code PDB: 2JMU. Thiamine-diphosphate kinase Hashitani Y, Cooper JR (1972). "The partial purification of thiamine triphosphatase from rat brain"
Thiamine-triphosphatase
Chemical compound
to thiamine pyrophosphate (ThDP) by a specific thiamine-triphosphatase. It can also be converted into ThDP by thiamine-diphosphate kinase. Thiamine triphosphate
Thiamine_triphosphate
Protein family
the biosynthesis of thiamine (vitamin B1), together with that catalysed by hydroxymethylpyrimidine kinase. Hydroxyethylthiazole kinase expression is regulated
Hydroxyethylthiazole_kinase
Class of enzymes
name of this enzyme class is ATP:thiamine diphosphotransferase. Other names in common use include thiamin kinase, thiamine pyrophosphokinase, ATP:thiamin
Thiamine_diphosphokinase
1.86: NADH kinase EC 2.7.1.87: streptomycin 3′′-kinase EC 2.7.1.88: dihydrostreptomycin-6-phosphate 3′α-kinase EC 2.7.1.89: thiamine kinase EC 2.7.1.90:
List_of_EC_numbers_(EC_2)
Metabolic disease
by a blockage in the enzyme thiamine-diphosphate kinase, and therefore treatment in some patients would be to take thiamine triphosphate daily. While the
Leigh_syndrome
toxopyrimidine by the enzyme hydroxymethylpyrimidine kinase. These reactions are steps in the biosynthesis of thiamine (vitamin B1). This enzyme is a transferase
Phosphomethylpyrimidine kinase
Phosphomethylpyrimidine_kinase
also called hydroxymethylpyrimidine kinase (phosphorylating). Lewin LM, Brown GM (1961). "The biosynthesis of thiamine. III. Mechanism of enzymatic formation
Hydroxymethylpyrimidine kinase
Hydroxymethylpyrimidine_kinase
Enzyme
In enzymology, a polyphosphate kinase (EC 2.7.4.1), or polyphosphate polymerase, is an enzyme that catalyzes the formation of polyphosphate from ATP, with
Polyphosphate_kinase
Protein-coding gene in the species Homo sapiens
lipoamide kinase isozyme 1, mitochondrial is an enzyme that in humans is encoded by the PDK1 gene. It codes for an isozyme of pyruvate dehydrogenase kinase (PDK)
Pyruvate dehydrogenase lipoamide kinase isozyme 1
Pyruvate_dehydrogenase_lipoamide_kinase_isozyme_1
RNA secondary structure
directly bind the riboswitch, as it does not require thiamine kinase to work in E. coli like thiamine itself or other analogues.) Nevertheless, there remains
TPP_riboswitch
Effect of alcohol consumption on the brain
supplementation of the diet by thiamine and an awareness by health professionals to treat 'at risk' patients with thiamine. Thiamine deficiency may occur in
Long-term impact of alcohol on the brain
Long-term_impact_of_alcohol_on_the_brain
Thaumatin Topoisomerase Tyrosine kinase Testosterone Tetrahydrocannabinol (THC) Tetracycline Thapsigargin Thaumatin Thiamine (vitamin B1) – C12H17ClN4OS·HCl
List_of_biomolecules
Protein-coding gene in the species Homo sapiens
dehydrogenase kinase. This gene is a member of the PDK/BCKDK protein kinase family and encodes a mitochondrial protein with a histidine kinase domain. This
PDK4
Chemical compound
(also known as OT) is a chemical analog of vitamin B1 (thiamine) and is classified as a thiamine antagonist. In the body, it is converted into its active
Oxythiamine
Autosomal recessive metabolic disorder
Intermediate maple syrup urine disease Intermittent maple syrup urine disease Thiamine-responsive maple syrup urine disease E3-deficient maple syrup urine disease
Maple_syrup_urine_disease
Class of enzymes
dihydrolipoamide and carbon dioxide. The conversion requires the coenzyme thiamine pyrophosphate. Pyruvate dehydrogenase is usually encountered as a component
Pyruvate_dehydrogenase
Protein that responds to low oxygen
or hypoxia. They also respond to instances of pseudohypoxia, such as thiamine deficiency. Both hypoxia and pseudohypoxia leads to impairment of adenosine
Hypoxia-inducible_factor
Protein-coding gene in the species Homo sapiens
protein, that exists as a homodimer, which catalyzes the conversion of thiamine to thiamine pyrophosphate. Alternate transcriptional splice variants, encoding
TPK1
Metabolic pathway
PP (2003), "Alpha-oxidation of 3-methyl-substituted fatty acids and its thiamine dependence", European Journal of Biochemistry, 270 (8): 1619–1627, doi:10
Alpha_oxidation
Non-protein chemical compound or metallic ion
cycle requires five organic cofactors and one metal ion: loosely bound thiamine pyrophosphate (TPP), covalently bound lipoamide and flavin adenine dinucleotide
Cofactor_(biochemistry)
Species of bacterium
synthase) and thieE (thiamine phosphate synthase) allows the strain to synthesize essential vitamins including biotin, vitamin B12, and thiamine. This evaluation
Heyndrickxia_coagulans
Multienzyme complex
acid residues (Asp, Asn, and Tyr) located on the alpha chain, and the thiamine diphosphate (TPP) cofactor directly involved in decarboxylation of the
Pyruvate dehydrogenase complex
Pyruvate_dehydrogenase_complex
Enzyme with key regulatory roles in most cells
proteins, either transcription factors, enzymes (e.g., cAMP-dependent kinases), or ion transporters. The first class of adenylyl cyclases occur in many
Adenylyl_cyclase
Class of enzyme
Nucleoside-diphosphate Uridylate Guanylate Thiamine-diphosphate 2.7.6: diphosphotransferase (P2O7) Ribose-phosphate diphosphokinase Thiamine diphosphokinase 2.7.7:
Cyclic_GMP-AMP_synthase
episode. Biochemically, arsenic prevents use of thiamine resulting in a clinical picture resembling thiamine deficiency. Poisoning with arsenic can raise
Arsenic_biochemistry
Scientific discipline
beverages with thiamine. Ingesting a diet rich in thiamine may stave off the adverse effects of deficiency. Foods providing rich sources of thiamine include
Nutritional_neuroscience
Illness from ingesting arsenic
Biochemically, arsenic prevents the use of thiamine resulting in a clinical picture resembling thiamine deficiency. Poisoning with arsenic can raise
Arsenic_poisoning
Multienzyme complex
catalyzed by the BCKDC. The role of each subunit is as follows: E1 uses thiamine pyrophosphate (TPP) as a catalytic cofactor. E1 catalyzes both the decarboxylation
Branched-chain alpha-keto acid dehydrogenase complex
Branched-chain_alpha-keto_acid_dehydrogenase_complex
Transport protein
receptor's tyrosine-kinase domain. The receptor then recruits Insulin Receptor Substrate, or IRS-1, which binds the enzyme PI-3 kinase. PI-3 kinase converts the
GLUT4
Large biological molecule that acts as a catalyst
such as flavin mononucleotide (FMN), flavin adenine dinucleotide (FAD), thiamine pyrophosphate (TPP), and tetrahydrofolate (THF), are derived from vitamins
Enzyme
Edible berry
Girardin, Ariane; Lefebvre, Benoit (April 2016). "The LysM receptor-like kinase Sl LYK 10 regulates the arbuscular mycorrhizal symbiosis in tomato". New
Tomato
Chemical compound of sulfur and oxygen
lowering the MAPK activity and activating adenylyl cyclase and protein kinase A. Smooth muscle cell proliferation is one of important mechanisms of hypertensive
Sulfur_dioxide
Transmembrane protein that moves ions across a biological membrane
Examples of the P-type ATPase include Na+/K+-ATPase that is regulated by Janus Kinase-2 as well as Ca2+ ATPase which exhibits sensitivity to ADP and ATP concentrations
Ion_transporter
Protein-coding gene in the species Homo sapiens
anhydrase enzyme, which also makes bicarbonate. Protein kinase C stimulates NHE3, while protein kinase A inhibits it. There is a specific protein functioning
Sodium–hydrogen_antiporter_3
Protein-coding gene in the species Homo sapiens
intermittent, thiamine-responsive and E3 deficient. The form of disease is dependent upon clinical prognosis, dietary protein tolerance, and thiamine response
BCKDHA
development and behavior. Korsakoff syndrome A chronic memory disorder caused by thiamine (vitamin B1) deficiency, most commonly due to chronic alcohol misuse. It
Glossary_of_neuroscience
Mammalian protein found in Homo sapiens
membrane. It is hypothesized that the protein contains protein kinase A and protein kinase C phosphorylation sites, which serve to regulate the proteins
Sodium/glucose cotransporter 1
Sodium/glucose_cotransporter_1
Family of transport proteins
structure-based identification of OATP modulation was developed. Since tyrosine kinase inhibitors (TKIs) are metabolized in the liver, interaction of TKIs with
Organic anion transporter family
Organic_anion_transporter_family
Interconnected biochemical reactions releasing energy
GDP-forming succinyl-CoA synthetase may be utilized by nucleoside-diphosphate kinase to form ATP (the catalyzed reaction is GTP + ADP → GDP + ATP). Products
Citric_acid_cycle
Mammalian protein found in Homo sapiens
phosphorylates DAT through protein kinase A (PKA) and protein kinase C (PKC) signaling. Phosphorylation by either protein kinase can result in DAT internalization
Dopamine_transporter
Protein-coding gene in the species Homo sapiens
Sodium-hydrogen exchange regulatory cofactor NHE-RF2 (NHERF-2) also known as tyrosine kinase activator protein 1 (TKA-1) or SRY-interacting protein 1 (SIP-1) is a protein
Sodium-hydrogen exchange regulatory cofactor 2
Sodium-hydrogen_exchange_regulatory_cofactor_2
Pain affecting the somatosensory nervous system
1055/s-0029-1211460. PMID 8886748. Thornalley PJ (2005). "The potential role of thiamine (vitamin B(1)) in diabetic complications". Curr Diabetes Rev. 1 (3): 287–98
Neuropathic_pain
Medical condition
affects step 5 of glycolysis. Phosphoglycerate kinase deficiency affects step 7 of glycolysis. Pyruvate kinase deficiency affects the 10th and last step of
Inborn errors of carbohydrate metabolism
Inborn_errors_of_carbohydrate_metabolism
Chemical compound and essential nutrient
Institute of Medicine, Food and Nutrition Board. Dietary reference intakes for Thiamine, Riboflavin, Niacin, Vitamin B6, Folate, Vitamin B12, Pantothenic Acid
Choline
acceptor) Glucose oxidase EC 1.1.3.4 L-Gulonolactone oxidase EC 1.1.3.8 Thiamine oxidase EC 1.1.3.23 Xanthine oxidase EC 1.1.3.32 Category:EC 1.1.4 (with
List_of_enzymes
Protein families
Gram-negative bacteria. The C-domain has been shown to possess tyrosine protein kinase activity, so it may function in a regulatory capacity. The lipopolysaccharide
MOP_flippase
vitamin B3 deficiency) Selenium deficiency Vitamin B1 deficiency (beriberi, thiamine deficiency) Vitamin B12 deficiency (cyanocobalamin deficiency) Vitamin
List_of_skin_conditions
Protein-coding gene in the species Homo sapiens
coenzymes required throughout the 5 steps that this complex carries out: thiamine pyrophosphate (TPP), lipoamide, and coenzyme A. This step is only one of
Pyruvate dehydrogenase (lipoamide) alpha 2
Pyruvate_dehydrogenase_(lipoamide)_alpha_2
Protein-coding gene in the species Homo sapiens
coenzymes required throughout the 5 steps that this complex carries out: thiamine pyrophosphate (TPP), lipoamide, and coenzyme A. This step is only one of
Pyruvate dehydrogenase (lipoamide) beta
Pyruvate_dehydrogenase_(lipoamide)_beta
Protein-coding gene in the species Homo sapiens
S (1995). "Characterization of a protein cofactor that mediates protein kinase A regulation of the renal brush border membrane Na(+)-H+ exchanger". J.
Sodium-hydrogen antiporter 3 regulator 1
Sodium-hydrogen_antiporter_3_regulator_1
Mammalian protein found in Homo sapiens
Phe215----Cys missense mutation in the dihydrolipoyl transacylase (E2) mRNA from a thiamine-responsive maple syrup urine disease patient WG-34". Biochem. Biophys.
DBT_(gene)
Genus of bacteria
nutritional requirements, all need biotin to grow. Some strains also need thiamine and PABA. Some of the Corynebacterium species with sequenced genomes have
Corynebacterium
affecting phosphorylation status of the α-arrestins where endocytosis of thiamine transporter, Thi7, mediated by Ecm21 requires TORC1 activity, but is independent
Alpha_Arrestin
Protein found in humans
A, Vékony N, Gassner D, et al. (2006). "Activation of classical protein kinase C reduces the expression of human cationic amino acid transporter 3 (hCAT-3)
Cationic amino acid transporter 3
Cationic_amino_acid_transporter_3
Mammalian protein found in Homo sapiens
occur and, instead, the increase in cAMP can be followed by PKA (Protein kinase A) activation and, as a result, the activation of the transcription factor
Sodium/iodide_cotransporter
Protein-coding gene in the species Homo sapiens
understood mechanisms include phosphorylation by the second messenger protein kinase C (PKC). PKC has been shown to inhibit NET function by sequestration of
Norepinephrine_transporter
Uniporter protein
transmembrane transporter activity transporter activity protein self-association kinase binding protein binding identical protein binding dehydroascorbic acid transmembrane
GLUT1
Protein-coding gene in the species Homo sapiens
coenzymes required throughout the 5 steps that this complex carries out: thiamine pyrophosphate (TPP), lipoamide, and coenzyme A. This step is only one of
Pyruvate dehydrogenase (lipoamide) alpha 1
Pyruvate_dehydrogenase_(lipoamide)_alpha_1
Protein found in humans
amino acid transporter EAAT5 by the serum and glucocorticoid dependent kinases SGK1 and SGK3". Biochem. Biophys. Res. Commun. 329 (2): 738–42. doi:10
Excitatory amino acid transporter 5
Excitatory_amino_acid_transporter_5
Protein found in humans
cytoplasmic domains. The terminal cytoplasmic domains can be phosphorylated by kinases within the neuron for rapid regulation. There are two isoforms of KCC2:
Chloride potassium symporter 5
Chloride_potassium_symporter_5
Order of eukaryotes
ethanol for energy expenditure and growth. In addition, vitamins such as thiamine, biotin, cobalamin, nicotinic acid, pantothenic acid, and riboflavin are
Thraustochytrid
Protein found in humans
(July 2003). "Phorbol myristate acetate-dependent interaction of protein kinase Calpha and the neuronal glutamate transporter EAAC1". The Journal of Neuroscience
Excitatory amino acid transporter 3
Excitatory_amino_acid_transporter_3
Mammalian protein found in Homo sapiens
cAMP activates protein kinase A, causing its active C subunits to be freed from its regulatory R subunits. Active protein kinase A, in turn, phosphorylates
Thermogenin
Gene family
25 The Biotin Uptake Transporter (BioMNY) Family 3.A.1.26 The Putative Thiamine Uptake Transporter (ThiW) Family 3.A.1.28 The Queuosine (Queuosine) Family
ABC_transporter
Protein found in humans
Watanabe N, Okamoto K, Komada H, Sakurai M, Ito Y (1998). "Protein tyrosine kinase activation provides an early and obligatory signal in anti-FRP-1/CD98/4F2
4F2 cell-surface antigen heavy chain
4F2_cell-surface_antigen_heavy_chain
Enzyme
cofactors in addition to the enzymes that make up the complex. The first is thiamine pyrophosphate (TPP), which is used by pyruvate dehydrogenase to oxidize
Dihydrolipoyl_transacetylase
map kinase kinase kinase 1 MeSH D08.811.913.696.620.682.700.559.200 – map kinase kinase kinase 2 MeSH D08.811.913.696.620.682.700.559.300 – map kinase kinase
List_of_MeSH_codes_(D08)
Mammalian protein found in Homo sapiens
lactate clearance from muscle after exercise, and elevated serum creatine kinase. ENSG00000281917 GRCh38: Ensembl release 89: ENSG00000155380, ENSG00000281917
Monocarboxylate_transporter_1
Protein found in humans
endoplasmic reticulum membrane Biological process positive regulation of I-kappaB kinase/NF-kappaB signaling 3'-phosphoadenosine 5'-phosphosulfate biosynthetic process
Adenosine 3'-phospho 5'-phosphosulfate transporter 1
Adenosine_3'-phospho_5'-phosphosulfate_transporter_1
Thalassemias, beta-; 604131; HBB Thanatophoric dysplasia, type I; 187600; FGFR3 Thiamine-responsive megaloblastic anemia syndrome; 249270; SLC19A2 Three M syndrome
List_of_OMIM_disorder_codes
Protein-coding gene in the species Homo sapiens
fructose stimulus ion transport transepithelial chloride transport protein kinase C signaling anion transport transepithelial transport cellular response
SLC26A6
Protein-coding gene in the species Homo sapiens
activity cation:chloride symporter activity symporter activity protein kinase binding potassium:chloride symporter activity Cellular component integral
SLC12A7
Protein-coding gene in the species Homo sapiens
Yan W, Nehrke K, Choi J, Barber DL (August 2001). "The Nck-interacting kinase (NIK) phosphorylates the Na+-H+ exchanger NHE1 and regulates NHE1 activation
Sodium–hydrogen_antiporter_1
Protein found in humans
fusion transcript with another gene called MAP3K9, that encodes for MAP3 kinase enzyme. This SLC39A9-MAP3K9 fusion gene has a repetitive occurrence in breast
Zinc_transporter_ZIP9
Membrane protein involved in transportation
a membrane transport protein is phosphorylated by a particular protein kinase, which is an enzyme that adds a phosphate group to proteins. (Grouped by
Membrane_transport_protein
Protein-coding gene in the species Homo sapiens
neuron-specific Na+/H+ exchanger NHE5 isoform. Regulation by phosphatidylinositol 3'-kinase and the actin cytoskeleton". J. Biol. Chem. 277 (45): 42623–32. doi:10.1074/jbc
Sodium/hydrogen_exchanger_5
Catabolic process in wide variety of organisms
sulfofructose to release erythrose (catalyzed by sulfofructose transketolase, a thiamine diphosphate dependent enzyme), and transfer of the C2-moiety to glyceraldehyde
Sulfoglycolysis
Protein-coding gene in the species Homo sapiens
at the plasma membrane. Some NCC modulators, such as the WNK3 and WNK4 kinases may regulate the amount of NCC at the cell surface by inducing the insertion
Sodium-chloride_symporter
Protein-coding gene in the species Homo sapiens
"Regulation of human organic anion transporter 4 by progesterone and protein kinase C in human placental BeWo cells". Am. J. Physiol. Endocrinol. Metab. 293
SLC22A9
Protein found in humans
cation:chloride symporter activity symporter activity transporter activity protein kinase binding potassium:chloride symporter activity Cellular component lysosomal
Chloride potassium symporter 4
Chloride_potassium_symporter_4
Protein-coding gene in the species Homo sapiens
acid metabolic process positive regulation of protein serine/threonine kinase activity response to insulin negative regulation of phospholipid biosynthetic
Long-chain fatty acid transport protein 1
Long-chain_fatty_acid_transport_protein_1
Protein-coding gene in the species Homo sapiens
(2006). "Stimulation of the creatine transporter SLC6A8 by the protein kinases SGK1 and SGK3". Biochem. Biophys. Res. Commun. 334 (3): 742–6. doi:10.1016/j
Sodium- and chloride-dependent creatine transporter 1
Sodium-_and_chloride-dependent_creatine_transporter_1
Classification of membrane proteins including ion channels
Biosynthesis Na+ Channel, FlaH (FlaH) Family 1.A.105 The Mixed Lineage Kinase Domain-like (MLKL) Family 1.A.106 The Calcium Load-activated Calcium Channel
Transporter Classification Database
Transporter_Classification_Database
Protein found in humans
memory formation by acting through the extracellular signal-regulated kinases signaling pathway. Angiotensin II-induced senescence of vascular smooth
Zinc_transporter_3
Protein-coding gene in the species Homo sapiens
S2CID 218864718. Beckman ML, Bernstein EM, Quick MW (August 1998). "Protein kinase C regulates the interaction between a GABA transporter and syntaxin 1A"
GABA_transporter_type_1
Protein found in humans
at the SGK1 consensus site is required for transport modulation by the kinase". J. Neurochem. 102 (3): 858–66. doi:10.1111/j.1471-4159.2007.04585.x. PMID 17442044
Excitatory amino acid transporter 4
Excitatory_amino_acid_transporter_4
Mammalian protein found in Homo sapiens
of the human vitamin C transporters expressed in COS-1 cells by protein kinase C [corrected]". American Journal of Physiology. Cell Physiology. 283 (6):
SLC23A1
Mammalian protein found in Homo sapiens
for dephosphorylation of neuronal Ca2+ channels phosphorylated by protein kinase C". The Journal of Neuroscience. 25 (8): 1914–23. doi:10.1523/JNEUROSCI
Choline transporter-like protein 1
Choline_transporter-like_protein_1
Protein-coding gene in the species Homo sapiens
there are five potential sites for protein-kinase C-dependent phosphorylation and one for protein-kinase A-dependent phosphorylation. Cryo-EM structures
SLC22A5
CDP-diacylglycerol diphosphatase EC 3.6.1.27: undecaprenyl-diphosphatase EC 3.6.1.28: thiamine-triphosphatase EC 3.6.1.29: bis(5′-adenosyl)-triphosphatase EC 3.6.1.30:
List_of_EC_numbers_(EC_3)
Protein-coding gene in the species Homo sapiens
PAH transporter: narrow substrate specificity and regulation by protein kinase C". Am J Physiol. 276 (2 Pt 2): F295–303. doi:10.1152/ajprenal.1999.276
Organic_anion_transporter_1
Protein found in humans
in adenoma (dra) gene product binds to the second PDZ domain of the NHE3 kinase A regulatory protein (E3KARP), potentially linking intestinal Cl-/HCO3-
Chloride_anion_exchanger
Protein family
phosphofructokinase, aldolase, hemoglobin, hemichromes, and the protein tyrosine kinase (p72syk). In humans, anion exchangers fall under the solute carrier family
Anion_exchanger_family
Protein-coding gene in the species Homo sapiens
specific granule membrane Biological process positive regulation of I-kappaB kinase/NF-kappaB signaling phosphatidylcholine biosynthetic process choline transport
Choline transporter-like protein 2
Choline_transporter-like_protein_2
Protein-coding gene in the species Homo sapiens
production negative regulation of cytokine production activation of protein kinase activity positive regulation of transcription by RNA polymerase II cellular
Natural resistance-associated macrophage protein 1
Natural_resistance-associated_macrophage_protein_1
THIAMINE KINASE
THIAMINE KINASE
THIAMINE KINASE
THIAMINE KINASE
THIAMINE KINASE
THIAMINE KINASE
THIAMINE KINASE
THIAMINE KINASE
n.
A hypothetic radical (C6H4) occurring in certain derivatives of benzene; as, phenylene diamine.
n.
A red or violet dyestuff having a greenish metallic luster. It is produced artificially, by the chemical dehydration of thionine, as a brown amorphous powder.
n.
Alt. of Theatine
n.
A weak nitrogenous sulphur base, C6H13NS2.
a.
A prefix or combining form of Diamine. [Also used adjectively.]
n.
Any compound containing two amido groups united with one or more acid or negative radicals, -- as distinguished from a diamine. Cf. Amido acid, under Amido, and Acid amide, under Amide.
n.
An amine containing three amido groups.
n.
One of an order of Italian monks, established in 1524, expressly to oppose Reformation, and to raise the tone of piety among Roman Catholics. They hold no property, nor do they beg, but depend on what Providence sends. Their chief employment is preaching and giving religious instruction.
n.
A nontoxic diamine, C4H12N2, formed in the putrefaction of the flesh of mammals and some other animals.
n.
A beautiful fluorescent crystalline substance, intermediate in composition between thionol and thionine.
n.
Alt. of Taminy
n.
An amide containing three amido groups.
n.
One of an order of nuns founded by Ursula Benincasa, who died in 1618.
n.
An artificial red or violet dyestuff consisting of a complex sulphur derivative of certain aromatic diamines, and obtained as a dark crystalline powder; -- called also phenylene violet.
n.
A compound containing two amido groups united with one or more basic or positive radicals, -- as contrasted with a diamide.