Title : Structure-activity relationship for the endogenous cannabinoid, anandamide, and certain of its analogues at vanilloid receptors in transfected cells and vas deferens.

Pub. Date : 2001 Feb

PMID : 11159715






8 Functional Relationships(s)
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1 2. pK(i) values for displacement of [(3)H]-resiniferatoxin from membranes of rVR1 transfected CHO cells were significantly less for anandamide (5.78) than for its structural analogues N-(4-hydroxyphenyl)-arachidonylamide (AM404; 6.18) and N-(3-methoxy-4-hydroxy)benzyl-arachidonylamide (arvanil; 6.77). [(3)h]-resiniferatoxin transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
2 2. pK(i) values for displacement of [(3)H]-resiniferatoxin from membranes of rVR1 transfected CHO cells were significantly less for anandamide (5.78) than for its structural analogues N-(4-hydroxyphenyl)-arachidonylamide (AM404; 6.18) and N-(3-methoxy-4-hydroxy)benzyl-arachidonylamide (arvanil; 6.77). CAV protocol transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
3 2. pK(i) values for displacement of [(3)H]-resiniferatoxin from membranes of rVR1 transfected CHO cells were significantly less for anandamide (5.78) than for its structural analogues N-(4-hydroxyphenyl)-arachidonylamide (AM404; 6.18) and N-(3-methoxy-4-hydroxy)benzyl-arachidonylamide (arvanil; 6.77). anandamide transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
4 3. pEC(50) values for stimulating (45)Ca(2+) uptake into rVR1 transfected CHO cells were significantly less for anandamide (5.80) than for AM404 (6.32) or arvanil (9.29). CAV protocol transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
5 3. pEC(50) values for stimulating (45)Ca(2+) uptake into rVR1 transfected CHO cells were significantly less for anandamide (5.80) than for AM404 (6.32) or arvanil (9.29). anandamide transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
6 3. pEC(50) values for stimulating (45)Ca(2+) uptake into rVR1 transfected CHO cells were significantly less for anandamide (5.80) than for AM404 (6.32) or arvanil (9.29). N-(4-hydroxyphenyl)arachidonylamide transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
7 3. pEC(50) values for stimulating (45)Ca(2+) uptake into rVR1 transfected CHO cells were significantly less for anandamide (5.80) than for AM404 (6.32) or arvanil (9.29). arvanil transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus
8 In conclusion, anandamide and certain of its analogues have affinity and efficacy at the rat VR1 receptor. anandamide transient receptor potential cation channel, subfamily V, member 1 Rattus norvegicus