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HIV protease HIVSDB Homology Searches Using Chem-BLAST NIST
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HIVSDB Homology Searches Using Chem-BLAST

NIST

This page shows all the inhibitors which have at least one chosen (Chosen) group in common. When the query has resulted in several PDBID's, additional group may be chosen by clicking another fragment | ?. PubMed abstract may be viewd if available.

Current Page :1 Result pages :|1 |2

View Inhibitor 1BV71BV7.
Counteracting HIV-1 protease drug resistance: structural analysis of mutant proteases complexed with XV638 and SD146, cyclic urea amides with broad specificities.

Ala PJ, Huston EE, Klabe RM, Jadhav PK, Lam PY, Chang CH.


Biochemistry. 1998 Oct 27;37(43):15042-9. Abstract
Related 2-D structures, Cellular data, Anti-HIV enzyme data, References
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Fragments of 1BV7. (Click another fragment to search inhibitors using an additional fragment)
1,3-thiazolidin-2-amine 1,3-thiazolidin-2-amine 3-methylbenzaldehydeThis residue has been selected, You may select one other residue shown in this row 3-methylbenzaldehyde 5,6-dihydroxy-1,3-diazepan-2-one 5,6-dihydroxy-1,3-diazepan-2-one PHENYL PHENYL 1. :Structure, links & more 2. :Abstract, text data & more
End of this inhibitor 
View Inhibitor 1BV91BV9.
Counteracting HIV-1 protease drug resistance: structural analysis of mutant proteases complexed with XV638 and SD146, cyclic urea amides with broad specificities.

Ala PJ, Huston EE, Klabe RM, Jadhav PK, Lam PY, Chang CH.


Biochemistry. 1998 Oct 27;37(43):15042-9. Abstract
Related 2-D structures, Cellular data, Anti-HIV enzyme data, References
Restart from
Fragments of 1BV9. (Click another fragment to search inhibitors using an additional fragment)
1,3-thiazolidin-2-amine 1,3-thiazolidin-2-amine 3-methylbenzaldehydeThis residue has been selected, You may select one other residue shown in this row 3-methylbenzaldehyde 5,6-dihydroxy-1,3-diazepan-2-one 5,6-dihydroxy-1,3-diazepan-2-one PHENYL PHENYL 1. :Structure, links & more 2. :Abstract, text data & more
End of this inhibitor 
View Inhibitor 1BWA1BWA.
Counteracting HIV-1 protease drug resistance: structural analysis of mutant proteases complexed with XV638 and SD146, cyclic urea amides with broad specificities.

Ala PJ, Huston EE, Klabe RM, Jadhav PK, Lam PY, Chang CH.


Biochemistry. 1998 Oct 27;37(43):15042-9. Abstract
Related 2-D structures, Cellular data, Anti-HIV enzyme data, References
Restart from
Fragments of 1BWA. (Click another fragment to search inhibitors using an additional fragment)
1,3-thiazolidin-2-amine 1,3-thiazolidin-2-amine 3-methylbenzaldehydeThis residue has been selected, You may select one other residue shown in this row 3-methylbenzaldehyde 5,6-dihydroxy-1,3-diazepan-2-one 5,6-dihydroxy-1,3-diazepan-2-one PHENYL PHENYL 1. :Structure, links & more 2. :Abstract, text data & more
End of this inhibitor 
View Inhibitor 1BWB1BWB.
Counteracting HIV-1 protease drug resistance: structural analysis of mutant proteases complexed with XV638 and SD146, cyclic urea amides with broad specificities.

Ala PJ, Huston EE, Klabe RM, Jadhav PK, Lam PY, Chang CH.


Biochemistry. 1998 Oct 27;37(43):15042-9. Abstract
Related 2-D structures, Cellular data, Anti-HIV enzyme data, References
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Fragments of 1BWB. (Click another fragment to search inhibitors using an additional fragment)
1H-benzimidazol-2-amine 1H-benzimidazol-2-amine 3-methylbenzaldehydeThis residue has been selected, You may select one other residue shown in this row 3-methylbenzaldehyde 5,6-dihydroxy-1,3-diazepan-2-one 5,6-dihydroxy-1,3-diazepan-2-one PHENYL PHENYL 1. :Structure, links & more 2. :Abstract, text data & more
End of this inhibitor 
View Inhibitor 1G2K1G2K.
Synthesis and comparative molecular field analysis (CoMFA) of symmetric and nonsymmetric cyclic sulfamide HIV-1 protease inhibitors.

Schaal W, Karlsson A, Ahlsen G, Lindberg J, Andersson HO, Danielson UH, Classon B, Unge T, Samuelsson B, Hulten J, Hallberg A, Karlen A.


J Med Chem. 2001 Jan 18;44(2):155-69. Abstract
Related 2-D structures, Cellular data, Anti-HIV enzyme data, References
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Fragments of 1G2K. (Click another fragment to search inhibitors using an additional fragment)
1,2,7-thiadiazepane-4,5-diol_1,1-dioxide 1,2,7-thiadiazepane-4,5-diol_1,1-dioxide 3-methylbenzaldehydeThis residue has been selected, You may select one other residue shown in this row 3-methylbenzaldehyde PHENYL PHENYL methoxybenzene methoxybenzene methylamine methylamine 1. :Structure, links & more 2. :Abstract, text data & more
End of this inhibitor 
View Inhibitor 1QBR1QBR.
Cyclic urea amides: HIV-1 protease inhibitors with low nanomolar potency against both wild type and protease inhibitor resistant mutants of HIV.

Jadhav PK, Ala P, Woerner FJ, Chang CH, Garber SS, Anton ED, Bacheler LT.


J Med Chem. 1997 Jan 17;40(2):181-91. Abstract
Related 2-D structures, Cellular data, Anti-HIV enzyme data, References
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Fragments of 1QBR. (Click another fragment to search inhibitors using an additional fragment)
1,3-thiazolidin-2-amine 1,3-thiazolidin-2-amine 3-methylbenzaldehydeThis residue has been selected, You may select one other residue shown in this row 3-methylbenzaldehyde 5,6-dihydroxy-1,3-diazepan-2-one 5,6-dihydroxy-1,3-diazepan-2-one PHENYL PHENYL 1. :Structure, links & more 2. :Abstract, text data & more
End of this inhibitor 

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