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1437732 Item(s)

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Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
Elsulfavirine Chemicals Other A new-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) for the treatment of HIV-1 infections, the prodrug of the active compound VM-1500A.. DCC-DC11892-250mg

DCChemicals 		250 mg Login
Compare
Elsulfavirine Chemicals Other A new-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) for the treatment of HIV-1 infections, the prodrug of the active compound VM-1500A.. DCC-DC11892-1g

DCChemicals 		1 g Login
Compare
GNE-­781 Chemicals Other selective, GNE-781 is a potent, non-CNS penetrant, orally active CBP/p300 bromodomain inhibitor with IC50 of 0.94/1.2 nM in TR-FRET assays. DCC-DC11729-100mg

DCChemicals 		100 mg Login
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GNE-­781 Chemicals Other selective, GNE-781 is a potent, non-CNS penetrant, orally active CBP/p300 bromodomain inhibitor with IC50 of 0.94/1.2 nM in TR-FRET assays. DCC-DC11729-250mg

DCChemicals 		250 mg Login
Compare
GNE-­781 Chemicals Other selective, GNE-781 is a potent, non-CNS penetrant, orally active CBP/p300 bromodomain inhibitor with IC50 of 0.94/1.2 nM in TR-FRET assays. DCC-DC11729-1g

DCChemicals 		1 g Login
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TMP778 Chemicals Other TMP778 (TMP-778) is a potent, selective RORγt inhibitor with IC50 of 7 nM in FRET assays and 63 nM in IL-17 promoter assays, with no inverse agonist activity. DCC-DC11846-100mg

DCChemicals 		100 mg Login
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TMP778 Chemicals Other TMP778 (TMP-778) is a potent, selective RORγt inhibitor with IC50 of 7 nM in FRET assays and 63 nM in IL-17 promoter assays, with no inverse agonist activity. DCC-DC11846-250mg

DCChemicals 		250 mg Login
Compare
TMP778 Chemicals Other TMP778 (TMP-778) is a potent, selective RORγt inhibitor with IC50 of 7 nM in FRET assays and 63 nM in IL-17 promoter assays, with no inverse agonist activity. DCC-DC11846-1g

DCChemicals 		1 g Login
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KEA1-­97 Chemicals Other KEA1-97 (KEA 1-97) is a small molecule that disrupts the interaction of thioredoxin with caspase 3. DCC-DC11627-100mg

DCChemicals 		100 mg Login
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KEA1-­97 Chemicals Other KEA1-97 (KEA 1-97) is a small molecule that disrupts the interaction of thioredoxin with caspase 3. DCC-DC11627-250mg

DCChemicals 		250 mg Login
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KEA1-­97 Chemicals Other KEA1-97 (KEA 1-97) is a small molecule that disrupts the interaction of thioredoxin with caspase 3. DCC-DC11627-1g

DCChemicals 		1 g Login
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PF 05180999 Chemicals Other selective, PF-05180999 (PF 5180999) is a potent, brain-penetrating and orally bioavailable phosphodiesterase 2A (PDE2A) inhibitor with IC50 of 1 nM. DCC-DC11937-100mg

DCChemicals 		100 mg Login
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PF 05180999 Chemicals Other selective, PF-05180999 (PF 5180999) is a potent, brain-penetrating and orally bioavailable phosphodiesterase 2A (PDE2A) inhibitor with IC50 of 1 nM. DCC-DC11937-250mg

DCChemicals 		250 mg Login
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PF 05180999 Chemicals Other selective, PF-05180999 (PF 5180999) is a potent, brain-penetrating and orally bioavailable phosphodiesterase 2A (PDE2A) inhibitor with IC50 of 1 nM. DCC-DC11937-1g

DCChemicals 		1 g Login
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KPT-­6566 Chemicals Other KPT-6566 is a covalent PIN1 inhibitor selectively targets cancer cells by a dual mechanism of action. DCC-DC11276-10mg

DCChemicals 		10 mg Login
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Dotinurad Chemicals Other Dotinurad is a novel compound that exhibits a remarkable uric acid excretion-promoting action. DCC-DC11521-100mg

DCChemicals 		100 mg Login
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Dotinurad Chemicals Other Dotinurad is a novel compound that exhibits a remarkable uric acid excretion-promoting action. DCC-DC11521-250mg

DCChemicals 		250 mg Login
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Dotinurad Chemicals Other Dotinurad is a novel compound that exhibits a remarkable uric acid excretion-promoting action. DCC-DC11521-1g

DCChemicals 		1 g Login
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PK-­11195 Chemicals Other respectively)., PK 11195 is a ligand of translocator protein. It targets Leishmania chemotherapy (IC50s of 14.2 μM, 8.2 μM, 3.5 μM for L. amazonensis, L. major and L. braziliensis DCC-DC11640-100mg

DCChemicals 		100 mg Login
Compare
PK-­11195 Chemicals Other respectively)., PK 11195 is a ligand of translocator protein. It targets Leishmania chemotherapy (IC50s of 14.2 μM, 8.2 μM, 3.5 μM for L. amazonensis, L. major and L. braziliensis DCC-DC11640-250mg

DCChemicals 		250 mg Login
Compare
PK-­11195 Chemicals Other respectively)., PK 11195 is a ligand of translocator protein. It targets Leishmania chemotherapy (IC50s of 14.2 μM, 8.2 μM, 3.5 μM for L. amazonensis, L. major and L. braziliensis DCC-DC11640-1g

DCChemicals 		1 g Login
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BL-­1249 Chemicals Other Blocking, other DCC-DC11753-10mg

DCChemicals 		10 mg Login
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BL-­1249 Chemicals Other Blocking, other DCC-DC11753-50mg

DCChemicals 		50 mg Login
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BAY-­678 Chemicals Other BAY-678 is a cell-permeable inhibitor of human neutrophil elastase (HNE). DCC-DC11858-100mg

DCChemicals 		100 mg Login
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BAY-­678 Chemicals Other BAY-678 is a cell-permeable inhibitor of human neutrophil elastase (HNE). DCC-DC11858-250mg

DCChemicals 		250 mg Login
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Name Price
Elsulfavirine Login Elsulfavirine
Type Chemicals
Clone
Specific against Other
Appl. A new-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) for the treatment of HIV-1 infections, the prodrug of the active compound VM-1500A..
Host
Item no.
Amount 250 mg
Available
Elsulfavirine Login Elsulfavirine
Type Chemicals
Clone
Specific against Other
Appl. A new-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) for the treatment of HIV-1 infections, the prodrug of the active compound VM-1500A..
Host
Item no.
Amount 1 g
Available
GNE-­781 Login GNE-781
Type Chemicals
Clone
Specific against Other
Appl. selective, GNE-781 is a potent, non-CNS penetrant, orally active CBP/p300 bromodomain inhibitor with IC50 of 0.94/1.2 nM in TR-FRET assays.
Host
Item no.
Amount 100 mg
Available
GNE-­781 Login GNE-781
Type Chemicals
Clone
Specific against Other
Appl. selective, GNE-781 is a potent, non-CNS penetrant, orally active CBP/p300 bromodomain inhibitor with IC50 of 0.94/1.2 nM in TR-FRET assays.
Host
Item no.
Amount 250 mg
Available
GNE-­781 Login GNE-781
Type Chemicals
Clone
Specific against Other
Appl. selective, GNE-781 is a potent, non-CNS penetrant, orally active CBP/p300 bromodomain inhibitor with IC50 of 0.94/1.2 nM in TR-FRET assays.
Host
Item no.
Amount 1 g
Available
TMP778 Login TMP778
Type Chemicals
Clone
Specific against Other
Appl. TMP778 (TMP-778) is a potent, selective RORγt inhibitor with IC50 of 7 nM in FRET assays and 63 nM in IL-17 promoter assays, with no inverse agonist activity.
Host
Item no.
Amount 100 mg
Available
TMP778 Login TMP778
Type Chemicals
Clone
Specific against Other
Appl. TMP778 (TMP-778) is a potent, selective RORγt inhibitor with IC50 of 7 nM in FRET assays and 63 nM in IL-17 promoter assays, with no inverse agonist activity.
Host
Item no.
Amount 250 mg
Available
TMP778 Login TMP778
Type Chemicals
Clone
Specific against Other
Appl. TMP778 (TMP-778) is a potent, selective RORγt inhibitor with IC50 of 7 nM in FRET assays and 63 nM in IL-17 promoter assays, with no inverse agonist activity.
Host
Item no.
Amount 1 g
Available
KEA1-­97 Login KEA1-97
Type Chemicals
Clone
Specific against Other
Appl. KEA1-97 (KEA 1-97) is a small molecule that disrupts the interaction of thioredoxin with caspase 3.
Host
Item no.
Amount 100 mg
Available
KEA1-­97 Login KEA1-97
Type Chemicals
Clone
Specific against Other
Appl. KEA1-97 (KEA 1-97) is a small molecule that disrupts the interaction of thioredoxin with caspase 3.
Host
Item no.
Amount 250 mg
Available
KEA1-­97 Login KEA1-97
Type Chemicals
Clone
Specific against Other
Appl. KEA1-97 (KEA 1-97) is a small molecule that disrupts the interaction of thioredoxin with caspase 3.
Host
Item no.
Amount 1 g
Available
PF 05180999 Login PF 05180999
Type Chemicals
Clone
Specific against Other
Appl. selective, PF-05180999 (PF 5180999) is a potent, brain-penetrating and orally bioavailable phosphodiesterase 2A (PDE2A) inhibitor with IC50 of 1 nM.
Host
Item no.
Amount 100 mg
Available
PF 05180999 Login PF 05180999
Type Chemicals
Clone
Specific against Other
Appl. selective, PF-05180999 (PF 5180999) is a potent, brain-penetrating and orally bioavailable phosphodiesterase 2A (PDE2A) inhibitor with IC50 of 1 nM.
Host
Item no.
Amount 250 mg
Available
PF 05180999 Login PF 05180999
Type Chemicals
Clone
Specific against Other
Appl. selective, PF-05180999 (PF 5180999) is a potent, brain-penetrating and orally bioavailable phosphodiesterase 2A (PDE2A) inhibitor with IC50 of 1 nM.
Host
Item no.
Amount 1 g
Available
KPT-­6566 Login KPT-6566
Type Chemicals
Clone
Specific against Other
Appl. KPT-6566 is a covalent PIN1 inhibitor selectively targets cancer cells by a dual mechanism of action.
Host
Item no.
Amount 10 mg
Available
Dotinurad Login Dotinurad
Type Chemicals
Clone
Specific against Other
Appl. Dotinurad is a novel compound that exhibits a remarkable uric acid excretion-promoting action.
Host
Item no.
Amount 100 mg
Available
Dotinurad Login Dotinurad
Type Chemicals
Clone
Specific against Other
Appl. Dotinurad is a novel compound that exhibits a remarkable uric acid excretion-promoting action.
Host
Item no.
Amount 250 mg
Available
Dotinurad Login Dotinurad
Type Chemicals
Clone
Specific against Other
Appl. Dotinurad is a novel compound that exhibits a remarkable uric acid excretion-promoting action.
Host
Item no.
Amount 1 g
Available
PK-­11195 Login PK-11195
Type Chemicals
Clone
Specific against Other
Appl. respectively)., PK 11195 is a ligand of translocator protein. It targets Leishmania chemotherapy (IC50s of 14.2 μM, 8.2 μM, 3.5 μM for L. amazonensis, L. major and L. braziliensis
Host
Item no.
Amount 100 mg
Available
PK-­11195 Login PK-11195
Type Chemicals
Clone
Specific against Other
Appl. respectively)., PK 11195 is a ligand of translocator protein. It targets Leishmania chemotherapy (IC50s of 14.2 μM, 8.2 μM, 3.5 μM for L. amazonensis, L. major and L. braziliensis
Host
Item no.
Amount 250 mg
Available
PK-­11195 Login PK-11195
Type Chemicals
Clone
Specific against Other
Appl. respectively)., PK 11195 is a ligand of translocator protein. It targets Leishmania chemotherapy (IC50s of 14.2 μM, 8.2 μM, 3.5 μM for L. amazonensis, L. major and L. braziliensis
Host
Item no.
Amount 1 g
Available
BL-­1249 Login BL-1249
Type Chemicals
Clone
Specific against Other
Appl. Blocking, other
Host
Item no.
Amount 10 mg
Available
BL-­1249 Login BL-1249
Type Chemicals
Clone
Specific against Other
Appl. Blocking, other
Host
Item no.
Amount 50 mg
Available
BAY-­678 Login BAY-678
Type Chemicals
Clone
Specific against Other
Appl. BAY-678 is a cell-permeable inhibitor of human neutrophil elastase (HNE).
Host
Item no.
Amount 100 mg
Available
BAY-­678 Login BAY-678
Type Chemicals
Clone
Specific against Other
Appl. BAY-678 is a cell-permeable inhibitor of human neutrophil elastase (HNE).
Host
Item no.
Amount 250 mg
Available

1437732 Item(s)

per page

Page:
  1. 5
  2. 6
  3. 7
  4. 8
  5. 9
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