| Name | calmodulin |
|---|---|
| Synonyms | CALM; CAM; CALM 1; CALM 2; CALM 3; CALM1; CALM2; CALM3… |
| Name | sodium cyanide |
|---|---|
| CAS | sodium cyanide (Na(CN)) |
| PubMed | Abstract | RScore(About this table) | |
|---|---|---|---|
| 9748253 | Xia Y, Tsai AL, Berka V, Zweier JL: generation from endothelial nitric-oxide synthase. J Biol Chem. 1998 Oct 2;273(40):25804-8. A Ca2+/calmodulin-dependent and regulatory process.. |
2(0,0,0,2) | Details |
| 11287127 | Porasuphatana S, Tsai P, Pou S, Rosen GM: Involvement of the perferryl complex of synthase in the catalysis of secondary free radical formation. Biochim Biophys Acta. 2001 Apr 3;1526(1):95-104. The generation of CH (3)*CHOH by NOS I was found to be Ca (2+)/calmodulin dependent. Formation of CH (3)*CHOH was inhibited by substituting for or inclusion of the NOS inhibitors N (G)-nitro- methyl ester, N (G)-monomethyl- and the heme blocker, sodium cyanide. |
2(0,0,0,2) | Details |
| 6219742 | Scully SP, Segel GB, Lichtman MA: Plasma membrane vesicles prepared from unadhered monocytes: characterization of transport and the ATPase. Cell Calcium. 1982 Dec;3(6):515-30. Monocyte plasma membranes that were stripped of endogenous calmodulin by EGTA treatment showed a reduced level of uptake and ATPase activity. The ionophore A23187 completely inhibited accumulation while 5 mM sodium cyanide and 10 microM ouabain had no effect. |
2(0,0,0,2) | Details |
| 6097546 | Smith RJ, Iden SS, Bowman BJ: Activation of the human neutrophil secretory process with 5 (S),12 (R)-dihydroxy-6,14-cis-8,10-trans-eicosatetraenoic acid. Inflammation. 1984 Dec;8(4):365-84. The calmodulin antagonist, trifluoperazine (TFP), and the intracellular antagonist, 8-(N,N-diethylamino)-octyl-(3,4,5-trimethoxy) hydrochloride (TMB-8), caused a dose-related inhibition of enzyme release from LTB4-stimulated neutrophils. Sodium cyanide was inactive. |
1(0,0,0,1) | Details |
| 6872358 | Smith RJ, Bowman BJ, Iden SS: Characteristics of 1-O-hexadecyl- and 1-O-octadecyl-2-O-acetyl-sn-glyceryl-3--stimulated granule enzyme release from human neutrophils. Clin Immunol Immunopathol. 1983 Jul;28(1):13-28. Trifluoperazine, an inhibitor of calmodulin, caused a dose-related suppression of C18-AGEPC-induced degranulation. Sodium cyanide was inactive. |
1(0,0,0,1) | Details |
| 8382363 | Hanaoka K, Sakai O, Imai M, Yoshitomi K: Mechanisms of transport across the basolateral membrane of the rabbit cortical thick ascending limb of Henle's loop. Pflugers Arch. 1993 Jan;422(4):339-46. Calmodulin inhibitors (trifluoperazine or W-7) increased [Ca2+] i. |
1(0,0,0,1) | Details |
| 2434190 | Edstrom A, Ekstrom P, Kanje M, Sjoberg J: The use of the regenerating frog sciatic nerve for pharmacological studies of orthograde and retrograde axonal transport. Brain Res. 1987 Jan 13;401(1):34-42. Compound 48/80 (50 micrograms/ml), the most specific calmodulin inhibitor so far described, inhibited the transport along the same part of the nerve. |
1(0,0,0,1) | Details |