29-METHYLIDENE-2,3-OXIDOSQUALENE - A POTENT MECHANISM-BASED INACTIVATOR OF OXIDOSQUALENE CYCLASE

[1] 26-HYDROXYSQUALENE AND DERIVATIVES - SUBSTRATES AND INHIBITORS FOR SQUALENE EPOXIDASE [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1991, 1 (04) : 227 - 232

[2] BAI M, UNPUB

[3] ENANTIOSELECTIVE ENZYMATIC STEROL SYNTHESIS BY ULTRASONICALLY STIMULATED BAKERS-YEAST [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (02) : 604 - 606

[4] CATTEL L, 1989, Steroids, V53, P363, DOI 10.1016/0039-128X(89)90020-2

[5] STEREOSPECIFIC SYNTHESIS OF SQUALENOID EPOXIDE VINYL ETHERS AS INHIBITORS OF 2,3-OXIDOSQUALENE CYCLASE [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1988, (03): : 461 - 469

[6] N-OXIDE AS A POTENTIAL FUNCTION IN THE DESIGN OF ENZYME-INHIBITORS - APPLICATION TO 2,3-EPOXYSQUALENE-STEROL CYCLASES [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1985, (15) : 1054 - 1055

[7] CHANG TY, 1979, J BIOL CHEM, V254, P1258

[8] SEPARATION OF CYCLIZATION AND REARRANGEMENT PROCESSES OF LANOSTEROL BIOSYNTHESIS . ENZYMIC CONVERSION OF 20,21-DEHYDRO-2,3-OXIDOSQUALENE TO A DEHYDROPROTOSTEROL [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1969, 91 (08) : 2132 - &

[9] 2,3-IMINOSQUALENE A POTENT INHIBITOR OF ENZYMIC CYCLIZATION OF 2,3-OXIDOSQUALENE TO STEROLS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1967, 89 (11) : 2797 - &

[10] INVITRO INHIBITION OF ANIMAL AND HIGHER-PLANTS 2,3-OXIDOSQUALENE-STEROL CYCLASES BY 2-AZA-2,3-DIHYDROSQUALENE AND DERIVATIVES, AND BY OTHER AMMONIUM-CONTAINING MOLECULES [J]. BIOCHEMICAL PHARMACOLOGY, 1985, 34 (15) : 2765 - 2777

[1] 26-HYDROXYSQUALENE AND DERIVATIVES - SUBSTRATES AND INHIBITORS FOR SQUALENE EPOXIDASE [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1991, 1 (04) : 227 - 232

[2] BAI M, UNPUB

[3] ENANTIOSELECTIVE ENZYMATIC STEROL SYNTHESIS BY ULTRASONICALLY STIMULATED BAKERS-YEAST [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1988, 110 (02) : 604 - 606

[4] CATTEL L, 1989, Steroids, V53, P363, DOI 10.1016/0039-128X(89)90020-2

[5] STEREOSPECIFIC SYNTHESIS OF SQUALENOID EPOXIDE VINYL ETHERS AS INHIBITORS OF 2,3-OXIDOSQUALENE CYCLASE [J]. JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1988, (03): : 461 - 469

[6] N-OXIDE AS A POTENTIAL FUNCTION IN THE DESIGN OF ENZYME-INHIBITORS - APPLICATION TO 2,3-EPOXYSQUALENE-STEROL CYCLASES [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1985, (15) : 1054 - 1055

[7] CHANG TY, 1979, J BIOL CHEM, V254, P1258

[8] SEPARATION OF CYCLIZATION AND REARRANGEMENT PROCESSES OF LANOSTEROL BIOSYNTHESIS . ENZYMIC CONVERSION OF 20,21-DEHYDRO-2,3-OXIDOSQUALENE TO A DEHYDROPROTOSTEROL [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1969, 91 (08) : 2132 - &

[9] 2,3-IMINOSQUALENE A POTENT INHIBITOR OF ENZYMIC CYCLIZATION OF 2,3-OXIDOSQUALENE TO STEROLS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1967, 89 (11) : 2797 - &

[10] INVITRO INHIBITION OF ANIMAL AND HIGHER-PLANTS 2,3-OXIDOSQUALENE-STEROL CYCLASES BY 2-AZA-2,3-DIHYDROSQUALENE AND DERIVATIVES, AND BY OTHER AMMONIUM-CONTAINING MOLECULES [J]. BIOCHEMICAL PHARMACOLOGY, 1985, 34 (15) : 2765 - 2777