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HIV Protease

HIV Protease

HIV-1 protease (PR) is a retroviral aspartyl protease (retropepsin), an enzyme involved with peptide bond hydrolysis in retroviruses, that is essential for the life-cycle of HIV, the retrovirus that causes AIDS. HIV protease cleaves newly synthesized polyproteins (namely, Gag and Gag-Pol[3]) at nine cleavage sites to create the mature protein components of an HIV virion, the infectious form of a virus outside of the host cell. Without effective HIV protease, HIV virions remain uninfectious.
TargetMol
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Cat. No. Product Name CAS No. Purity Chemical Structure
T16973 TAK-220
化合物 T16973
333994-00-6 98%
TargetMol Chemical Structure TAK-220
TAK-220 is a selective and orally bioavailable CCR5 antagonist (IC50s: 3.5 nM and 1.4 nM for inhibition on the binding of RANTES and MIP-1α to CCR5, respectively...
TN3704 Coronalolide
化合物 TN3704
268214-51-3 98%
TargetMol Chemical Structure Coronalolide
Coronalolide shows significant cytotoxic activities in P-388 cell line, it also displays significant anti-HIV activities in the HIV-1RT assay. Coronalolide and c...
T14831 Bryostatin 1
苔藓抑素1
83314-01-6 98%
TargetMol Chemical Structure Bryostatin 1
Bryostatin 1 is a natural macrolide isolated from the bryozoan Bugula neritina and is a CNS)permeable PKC modulator. Bryostatin 1 binds to the isolated C1 domain...
T15683 L-689502
化合物 T15683
138483-63-3 98%
TargetMol Chemical Structure L-689502
L-689502 is a potent HIV-l protease inhibitor (IC50: 1 nM).
TN3119 5-Hydroxy-7,8-dimethoxyflavanone
5-羟基-7,8-二甲氧基黄烷酮
113981-49-0 98%
TargetMol Chemical Structure 5-Hydroxy-7,8-dimethoxyflavanone
5-Hydroxy-7,8-dimethoxyflavanone 是从穿心莲叶和根中分离出来的,具有抗炎活性。
TN4705 Oleoside
木犀榄苷
178600-68-5 98%
TargetMol Chemical Structure Oleoside
Oleoside 可从油橄榄和Zizyphus lotus L.树枝中提取,可能用于抑制HIV-1蛋白酶。
TN4605 Myriceric acid B
化合物 TN4605
55497-79-5 98%
TargetMol Chemical Structure Myriceric acid B
Myriceric acid B is a potent HIV-1 entry inhibitor targeting gp41 and can serve as a lead compound for developing novel anti-HIV-1 drug. Myriceric acid B scaveng...
TN5191 Tsugafolin
化合物 TN5191
66568-97-6 98%
TargetMol Chemical Structure Tsugafolin
Tsugafolin has weak anti-HIV activity.
TN1194 16beta,17-Dihydroxy-ent-kaurane-19-oic acid
ENT-16Α17-二羟基贝壳杉烷-18-羧酸
74365-74-5 98%
TargetMol Chemical Structure 16beta,17-Dihydroxy-ent-kaurane-19-oic acid
16beta,17-Dihydroxy-ent-kaurane-19-oic acid as an anti-HIV principle, it showed significant activity against HIV replication in H9 lymphocyte cells with an EC50 ...
T10111L 3-Deazaadenosine
3-脱氮腺苷
6736-58-9 98%
TargetMol Chemical Structure 3-Deazaadenosine
3-Deazaadenosine is an inhibitor of S-adenosylhomocysteine hydrolase, with a Ki of 3.9 µM, and it has anti-inflammatory, anti-proliferative and anti-HIV activity...
T22468 1-Deoxymannojirimycin hydrochloride
1-甘露糖野尻霉素盐酸盐
73465-43-7 98%
TargetMol Chemical Structure 1-Deoxymannojirimycin hydrochloride
1-Deoxymannojirimycin hydrochloride 是一种选择性的 α1,2-甘露糖苷酶抑制剂,IC50值为 20 μM。它还抑制 HIV-1 毒株,抗病毒活性较差。
TN5133 3',5,5',7-Tetrahydroxy-4',6-dimethoxyflavone
化合物 TN5133
125537-92-0 98%
TargetMol Chemical Structure 3',5,5',7-Tetrahydroxy-4',6-dimethoxyflavone
5,7,3',5'-tetrahydroxy-6,4'-dimethoxyflavone exhibits anti-HIV-1 activity in the anti-syncytium assay using (∆Tat/rev)MC99 virus and 1A2 cell line system, it sho...
TN1348 8-Prenylluteone
8-异戊烯基羽扇豆异黄酮
125002-91-7 98%
TargetMol Chemical Structure 8-Prenylluteone
8-Prenylluteone can potently inhibit HIV-1 PR activity.
TN1708 Gomisin M2
五味子脂素 M2
82425-45-4 98%
TargetMol Chemical Structure Gomisin M2
Gomisin M2 is an anti-HIV agent.
TN3152 6-Acetonyldihydrochelerythrine
化合物 TN3152
22864-92-2 98%
TargetMol Chemical Structure 6-Acetonyldihydrochelerythrine
6-Acetonyldihydrochelerythrine exhibits significant antioxidant activities, it exhibits significant anti-HIV activity in H9 lymphocytes with EC50 and TI (Therape...
T10928 Cytochalasin A
细胞松弛素A
14110-64-6 98%
TargetMol Chemical Structure Cytochalasin A
Cytochalasin A is a cell-permeable fungal toxin and is an oxidized derivative of cytochalasin B. Cytochalasin A is an inhibitor of HIV-1 protease (IC50 = 3 μM), ...
TN4584 Morolic acid
化合物 TN4584
559-68-2 98%
TargetMol Chemical Structure Morolic acid
Morolic acid and moronic acid have shown sustained antidiabetic and antihyperglycemic action possibly mediated by an insulin sensitization with consequent change...
T14559 BI 224436
化合物 T14559
1155419-89-8 98%
TargetMol Chemical Structure BI 224436
BI 224436 is an inhibitor of HIV-1 noncatalytic site integrase. With EC50 values of less than 15 nM against different HIV-1 laboratory strains.
TN3777 Daurichromenic acid
化合物 TN3777
82003-90-5 98%
TargetMol Chemical Structure Daurichromenic acid
Daurichromenic acid is a terpenophenol with a potent anti-HIV activity.
T16112 ML67-33
化合物 T16112
1443290-89-8 98%
TargetMol Chemical Structure ML67-33
ML67-33 rapidly and reversibly affects K2P2.1 (TREK-1) (EC50s: 36.3 μM and 9.7 μM in cell-free and HEK293 cells, respectively). ML67-33 is a selective activator ...
TAK-220
T16973
TAK-220 is a selective and orally bioavailable CCR5 antagonist (IC50s: 3.5 nM and 1.4 nM for inhibition on the binding of RANTES and MIP-1α to CCR5, respectively...
Coronalolide
TN3704
Coronalolide shows significant cytotoxic activities in P-388 cell line, it also displays significant anti-HIV activities in the HIV-1RT assay. Coronalolide and c...
Bryostatin 1
T14831
Bryostatin 1 is a natural macrolide isolated from the bryozoan Bugula neritina and is a CNS)permeable PKC modulator. Bryostatin 1 binds to the isolated C1 domain...
L-689502
T15683
L-689502 is a potent HIV-l protease inhibitor (IC50: 1 nM).
5-Hydroxy-7,8-dimethoxyflavanone
TN3119
5-Hydroxy-7,8-dimethoxyflavanone 是从穿心莲叶和根中分离出来的,具有抗炎活性。
Oleoside
TN4705
Oleoside 可从油橄榄和Zizyphus lotus L.树枝中提取,可能用于抑制HIV-1蛋白酶。
Myriceric acid B
TN4605
Myriceric acid B is a potent HIV-1 entry inhibitor targeting gp41 and can serve as a lead compound for developing novel anti-HIV-1 drug. Myriceric acid B scaveng...
Tsugafolin
TN5191
Tsugafolin has weak anti-HIV activity.
16beta,17-Dihydroxy-ent-kaurane-19-oic acid
TN1194
16beta,17-Dihydroxy-ent-kaurane-19-oic acid as an anti-HIV principle, it showed significant activity against HIV replication in H9 lymphocyte cells with an EC50 ...
3-Deazaadenosine
T10111L
3-Deazaadenosine is an inhibitor of S-adenosylhomocysteine hydrolase, with a Ki of 3.9 µM, and it has anti-inflammatory, anti-proliferative and anti-HIV activity...
1-Deoxymannojirimycin hydrochloride
T22468
1-Deoxymannojirimycin hydrochloride 是一种选择性的 α1,2-甘露糖苷酶抑制剂,IC50值为 20 μM。它还抑制 HIV-1 毒株,抗病毒活性较差。
3',5,5',7-Tetrahydroxy-4',6-dimethoxyflavone
TN5133
5,7,3',5'-tetrahydroxy-6,4'-dimethoxyflavone exhibits anti-HIV-1 activity in the anti-syncytium assay using (∆Tat/rev)MC99 virus and 1A2 cell line system, it sho...
8-Prenylluteone
TN1348
8-Prenylluteone can potently inhibit HIV-1 PR activity.
Gomisin M2
TN1708
Gomisin M2 is an anti-HIV agent.
6-Acetonyldihydrochelerythrine
TN3152
6-Acetonyldihydrochelerythrine exhibits significant antioxidant activities, it exhibits significant anti-HIV activity in H9 lymphocytes with EC50 and TI (Therape...
Cytochalasin A
T10928
Cytochalasin A is a cell-permeable fungal toxin and is an oxidized derivative of cytochalasin B. Cytochalasin A is an inhibitor of HIV-1 protease (IC50 = 3 μM), ...
Morolic acid
TN4584
Morolic acid and moronic acid have shown sustained antidiabetic and antihyperglycemic action possibly mediated by an insulin sensitization with consequent change...
BI 224436
T14559
BI 224436 is an inhibitor of HIV-1 noncatalytic site integrase. With EC50 values of less than 15 nM against different HIV-1 laboratory strains.
Daurichromenic acid
TN3777
Daurichromenic acid is a terpenophenol with a potent anti-HIV activity.
ML67-33
T16112
ML67-33 rapidly and reversibly affects K2P2.1 (TREK-1) (EC50s: 36.3 μM and 9.7 μM in cell-free and HEK293 cells, respectively). ML67-33 is a selective activator ...
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TargetMol Loading
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