| 1/2 RT | half-relaxation time |
|---|---|
| 1/2 RT | relaxation time |
| 10% O2 | of hypoxia |
| 10(-4) M | L-N(G)-nitroarginine methyl ester |
| 10(-4) M | N(G)-monomethyl-L-arginine |
| 10(-5) M | Meclofenamate |
| 10(-5) M | Methylene blue |
| 10(-6) M | Morphine |
| 10-EdAM | 10-Ethyl-10-deaza-aminopterin |
| 100 g | Glucose |
| 15-oxoprostaglandin 13-reductase | <enzyme> (5z)-(15s)-11 alpha-hydroxy-9,15-dioxoprostanoate:NAD(p)+ delta(13)-oxidoreductase. An enzyme active in prostaglandin e and f catabolism. It catalyses the reduction of the double bond at the 13-14 position of the 15-ketoprostaglandins and uses NADPH as cofactor. Registry number: EC 1.3.1.48 (12 Dec 1998) |
|---|---|
| 15O | Symbol for oxygen-15. (05 Mar 2000) |
| 16 alpha-hydroxyprogesterone dehydratase | <enzyme> From rat intestinal anaerobic bacteria; forms 16-dehydroprogesterone Registry number: EC 4.2.1.- Synonym: 16 alpha-dehydratase (26 Jun 1999) |
| 16,16-dimethylprostaglandin e2 | <chemical> (5z,11 alpha,13e,15r)-11,15-dihydroxy-16,16-dimethyl-9-oxoprosta-5,13-dien-1-oic acid. A synthetic prostaglandin e analog that protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. The protective effect is independent of acid inhibition. It is also a potent inhibitor of pancreatic function and growth of experimental tumours. Pharmacological action: anti-ulcer agents. Chemical name: Prosta-5,13-dien-1-oic acid, 11,15-dihydroxy-16,16-dimethyl-9-oxo-, (5Z,11alpha,13E,15R)- (12 Dec 1998) |
| 16-dehydroprogesterone reductase | <enzyme> Reduces 16-dehydroprogesterone to 17-isoprogesterone; neither NADH or NADPH with or without flavin nucleotides are used as electron donors Registry number: EC 1.3.99.- Synonym: 16-dhpr (26 Jun 1999) |
| 16-hydroxypalmitic acid hydroxylase | <enzyme> P-450 dependent hydroxylation of 16-hydroxypalmitic acid at the c9 or c10 position in the presence of NADPH and oxygen Registry number: EC 1.14.13.- (26 Jun 1999) |
| 16O | Symbol for oxygen-16. (05 Mar 2000) |
| 16S RNA pseudouridine 516 synthase | <enzyme> Acts only on uridine 516 of e. Coli 16s RNA; amino acid sequence given in first source Registry number: EC 5.4.99.- Synonym: psi516 synthase, rsua gene product (26 Jun 1999) |
| 17 alpha-hydroxyprogesterone aldolase | <enzyme> An enzyme of the lyase class that catalyses the cleavage of the bond between carbons 17 and 20 in 17-alpha hydroxyprogesterone to form delta 4-androstene-3,17-dione, an androgen. It also catalyses the conversion of 17 alpha-hydroxypregnenolone to dehydroepiandrosterone. Chemical name: 17 alpha-hydroxyprogesterone acetaldehyde-lyase Registry number: EC 4.1.2.30 (12 Dec 1998) |
| 17-epitestosterone | 17a-Hydroxyandrost-4-en-3-one; 17a-epimer of testosterone;a biologically inactive steroid found in testes and ovaries; may be a metabolite of 4-androstene-3,17-dione and a precursor of 17a-estradiol. (05 Mar 2000) |
| 17-hydroxycorticosteroid test | A test, dependent on the Porter-Silber reaction, that is used as a measure of adrenocortical function and is performed on urine. Low values are seen in Addison's disease and hypopituitarism; high values are seen in Cushing's syndrome and extreme stress. Synonym: 17-OH-corticoids test, Porter-Silber chromogens test. (05 Mar 2000) |
| 17-hydroxycorticosteroids | <biochemistry> A urine test which measures the amount of 17-hydroxycorticosteroids. A fraction of cortisol is metabolised to 17-hydroxycorticosteroids and excreted in the urine. Conditions that result in increased serum cortisol (Cushing's syndrome and Cushing's disease) will result in elevations in 17-hydroxycorticosteroid levels in the urine. (13 Nov 1997) |
| 17-hydroxylase deficiency syndrome | <syndrome> Congenital deficiency of adrenocortical, and possibly ovarian, steroid C-17a hydroxylase; the resulting excessive secretion of corticosterone and deoxycorticosterone produces hypertension and hypokalaemic alkalosis; absence of aldosterone secretion in such patients may indicate a multiple enzymic deficiency. (05 Mar 2000) |
| 17-hydroxyprogesterone | A hydroxyprogesterone with medical uses similar to that of progesterone. (12 Dec 1998) |
| 17-hydroxysteroid dehydrogenases | <enzyme> A class of enzymes that catalyses the oxidation of 17-hydroxysteroids to 17-ketosteroids. Registry number: EC 1.1.- (12 Dec 1998) |
Synonyms : 12 S Hydroxyeicosatetraenoic Acid, Acid, 12-S-Hydroxyeicosatetraenoic
Synonyms : 14-3-3 Protein, 14-3-3 Protein, beta Isoform, 14-3-3 Protein, epsilon Isoform, 14-3-3 Protein, eta Isoform, 14-3-3 Protein, gamma Isoform, 14-3-3 Protein, tau Isoform, 14-3-3 Protein, zeta Isoform, 14-3-3 beta Protein, 14-3-3 epsilon Protein, 14-3-3 eta Protein
Synonyms : (15S)-Hydroxy-11 alpha, 9 alpha-(epoxymethano)prosta-5Z, 13E-dienoic Acid, (15S)hydroxy-9alpha, 11alpha-(epoxymethano)prosta-5, 13-dienoic acid, 11 alpha, 9 alpha-Epoxymethano PGH2, 9, 11-Dideoxy-11 alpha, 9 alpha-epoxymethanoprostaglandin F2 alpha, U-44619
Synonyms : 15-Ketoprostaglandin delta 13-Reductase, delta 13-15-Ketoprostaglandin Reductase, delta-13-PG-Reductase, 13-15-Ketoprostaglandin Reductase, delta, 13-Reductase, 15-Ketoprostaglandin delta, 13-Reductase, 15-Oxoprostaglandin, 15 Oxoprostaglandin 13 Reductase
Synonyms : 16, 16-Dimethyl-PGE2, 16, 16 Dimethyl PGE2, 16, 16 Dimethylprostaglandin E2, E2, 16, 16-Dimethylprostaglandin
| 1,4-α-glucan branching enzyme |
[EC 2.4.1.18] an enzyme of the transferase class that catalyzes the cleavage of internal α-1,4-glucoside linkages in glycogen (or, in plants, amylopectin) and transfer of the fragments into α-1,6 linkages, thus creating branches in the glycogen molecule. Deficiency of the enzyme, an autosomal recessive trait, results in glycogen storage disease, type IV. Called also brancher or branching enzyme.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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|---|---|
| 1,4-diethylene dioxide |
dioxane.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| 1-phosphatidylinositol phosphodiesterase |
[EC 3.1.4.10] a phospholipase C specific for phosphoinositides, occurring in all tissues. It is part of a mechanism for mobilization of calcium in response to hormones; it is activated by hormonal binding via a G protein and begins the cycle of phosphoinositide metabolism. It can also play a role in the liberation of arachidonic acid from phosphatidylinositol.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| 1-pyrroline-5-carboxylate dehydrogenase |
[EC 1.5.1.12] an enzyme of the oxidoreductase class that catalyzes the dehydrogenation of Δ1-pyrroline 5-carboxylate to glutamate, using NAD+ as an electron acceptor; the reaction is a step in the degradation of proline and excess ornithine. The enzyme can also oxidize the 3-hydroxy derivative of Δ1-pyrroline 5-carboxylate to form 4-hydroxyglutamate. Deficiency of the enzyme, an autosomal recessive trait, is the cause of hyperprolinemia, type II.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
|
| 11β-h. |
steroid 11β-monooxygenase.
출처: www.mercksource.com/pp/us/cns/cns_health_library.j...
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| 1 | the ordinal number of one hundred fifty in counting order |
|---|---|
| 1 | the decade from 1530 to 1539 |
| 1 | being five more than one hundred fifty |
| 1 | the ordinal number of one hundred fifty-five in counting order |
| 1 | the date of Allied victory over Japan, World War II |
| 1 | coming next after the fourteenth and just before the sixteenth in position |
| 1 | the cardinal number that is the sum of fifteen and one |
| 1 | being one more than fifteen |
| 1 | being ten more than one hundred fifty |
| 1 | the ordinal number of one hundred sixty in counting order |
| 1 | being five more than one hundred sixty |
| 1 | the ordinal number of one hundred sixty-five in counting order |
