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Molecules

1437732 Item(s)

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  2. 8
  3. 9
  4. 10
  5. 11
Name PDF Type Clone Specific against Appl. Host Item no. Amount ✓ Price
DS-­6930 Chemicals Other IV DCC-DC12411-5mg

DCChemicals 		5 mg Login
Compare
STOML3 inhibitor OB-­1 Inhibitors Other IV DCC-DC20558-100mg

DCChemicals 		100 mg Login
Compare
GOT1 inhibitor 2c Inhibitors Other DCC-DC12542-1g

DCChemicals 		1 g Login
Compare
STOML3 inhibitor OB-­1 Inhibitors Other IV DCC-DC20558-250mg

DCChemicals 		250 mg Login
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JND3229 Inhibitors Other IV DCC-DC12804-250mg

DCChemicals 		250 mg Login
Compare
JND3229 Inhibitors Other IV DCC-DC12804-1g

DCChemicals 		1 g Login
Compare
Apararenone Chemicals Other Apararenone (MT-3995) is a novel potent, selective non-steroidal mineralocorticoid receptor antagonist for the treatment of diabetic nephropathies and non-alcoholic steatohepatitis.. DCC-DC12636-250mg

DCChemicals 		250 mg Login
Compare
Apararenone Chemicals Other Apararenone (MT-3995) is a novel potent, selective non-steroidal mineralocorticoid receptor antagonist for the treatment of diabetic nephropathies and non-alcoholic steatohepatitis.. DCC-DC12636-1g

DCChemicals 		1 g Login
Compare
PLB-­1001 Chemicals Other Bozitinib (PLB-1001) is a highly selective c-MET kinase inhibitor with blood-brain barrier permeability. Bozitinib (PLB-1001) is a ATP-competitive small-molecule inhibitor, binds to the conventional ATP-binding pocket of the tyrosine kinase superfamily[1]. DCC-DC12462-100mg

DCChemicals 		100 mg Login
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PLB-­1001 Chemicals Other Bozitinib (PLB-1001) is a highly selective c-MET kinase inhibitor with blood-brain barrier permeability. Bozitinib (PLB-1001) is a ATP-competitive small-molecule inhibitor, binds to the conventional ATP-binding pocket of the tyrosine kinase superfamily[1]. DCC-DC12462-250mg

DCChemicals 		250 mg Login
Compare
PLB-­1001 Chemicals Other Bozitinib (PLB-1001) is a highly selective c-MET kinase inhibitor with blood-brain barrier permeability. Bozitinib (PLB-1001) is a ATP-competitive small-molecule inhibitor, binds to the conventional ATP-binding pocket of the tyrosine kinase superfamily[1]. DCC-DC12462-1g

DCChemicals 		1 g Login
Compare
A4250 Chemicals Other A4250 (A-4250, Odevixibat) is a small molecule ileal bile acid transporter (IBAT) inhibitor for the treatment of cholestatic liver diseases including progressive familial intrahepatic cholestasis and NASH.. DCC-DC20611-1g

DCChemicals 		1 g Login
Compare
HS220 Chemicals Other HS220 (HS-220) is a Plasmodium-selective takinib analog that targets atypical P. falciparum protein kinase 9 (PfPK9, Kd=4.1 uM) but does not inhibit HsTAK1, decreases K63-linked ubiquitination in P. falciparum; inhibits P. berghei parasite load in HuH7 cells with EC50 of 43 uM, with no significant change on HuH7 viability; induce a unique phenotype where parasite size in hepatocytes increases. DCC-DC12632-250mg

DCChemicals 		250 mg Login
Compare
GDC-­0214(GDC0214) Chemicals Other GDC0214 is a potent, selective inhalable and lung-restricted inhibitor of JAK1 with IC50 of 8.52 nM, displays 6.3/704/28 fold selectivity over JAK2/JAK3/TYK2. DCC-DC12547-100mg

DCChemicals 		100 mg Login
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GDC-­0214(GDC0214) Chemicals Other GDC0214 is a potent, selective inhalable and lung-restricted inhibitor of JAK1 with IC50 of 8.52 nM, displays 6.3/704/28 fold selectivity over JAK2/JAK3/TYK2. DCC-DC12547-250mg

DCChemicals 		250 mg Login
Compare
GDC-­0214(GDC0214) Chemicals Other GDC0214 is a potent, selective inhalable and lung-restricted inhibitor of JAK1 with IC50 of 8.52 nM, displays 6.3/704/28 fold selectivity over JAK2/JAK3/TYK2. DCC-DC12547-1g

DCChemicals 		1 g Login
Compare
iGOT1-­01 Chemicals Other iGOT1-01 is a small molecule inhibitor of aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1 (GOT1)) with IC50 of 11.3 uM. DCC-DC12541-100mg

DCChemicals 		100 mg Login
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GLP-­1(7-­36), amide Chemicals Other DCC-DC10319-25mg

DCChemicals 		25 mg Login
Compare
iGOT1-­01 Chemicals Other iGOT1-01 is a small molecule inhibitor of aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1 (GOT1)) with IC50 of 11.3 uM. DCC-DC12541-1g

DCChemicals 		1 g Login
Compare
YTX-­465 Chemicals Other YTX-465 (YTX465) is a specific small molecule that rescues yeast from a-Syn cytotoxicity with EC50 of 15 nM, via inhibiting Ole1, the yeast homolog of human stearoyl-CoA desaturase (SCD). DCC-DC12618-100mg

DCChemicals 		100 mg Login
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YTX-­465 Chemicals Other YTX-465 (YTX465) is a specific small molecule that rescues yeast from a-Syn cytotoxicity with EC50 of 15 nM, via inhibiting Ole1, the yeast homolog of human stearoyl-CoA desaturase (SCD). DCC-DC12618-250mg

DCChemicals 		250 mg Login
Compare
Flupenthixol dihydrochloride Chemicals Other DCC-DC9164-100mg

DCChemicals 		100 mg Login
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Flupenthixol dihydrochloride Chemicals Other DCC-DC9164-250mg

DCChemicals 		250 mg Login
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5-­R-­Rivaroxaban Chemicals Other DCC-DC9444-10mg

DCChemicals 		10 mg Login
Compare
17-­AAG Chemicals Other DCC-DC9482-100mg

DCChemicals 		100 mg Login
Compare
Name Price
DS-­6930 Login DS-6930
Type Chemicals
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 5 mg
Available
STOML3 inhibitor OB-­1 Login STOML3 inhibitor OB-1
Type Inhibitors
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 100 mg
Available
GOT1 inhibitor 2c Login GOT1 inhibitor 2c
Type Inhibitors
Clone
Specific against Other
Appl.
Host
Item no.
Amount 1 g
Available
STOML3 inhibitor OB-­1 Login STOML3 inhibitor OB-1
Type Inhibitors
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 250 mg
Available
JND3229 Login JND3229
Type Inhibitors
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 250 mg
Available
JND3229 Login JND3229
Type Inhibitors
Clone
Specific against Other
Appl. IV
Host
Item no.
Amount 1 g
Available
Apararenone Login Apararenone
Type Chemicals
Clone
Specific against Other
Appl. Apararenone (MT-3995) is a novel potent, selective non-steroidal mineralocorticoid receptor antagonist for the treatment of diabetic nephropathies and non-alcoholic steatohepatitis..
Host
Item no.
Amount 250 mg
Available
Apararenone Login Apararenone
Type Chemicals
Clone
Specific against Other
Appl. Apararenone (MT-3995) is a novel potent, selective non-steroidal mineralocorticoid receptor antagonist for the treatment of diabetic nephropathies and non-alcoholic steatohepatitis..
Host
Item no.
Amount 1 g
Available
PLB-­1001 Login PLB-1001
Type Chemicals
Clone
Specific against Other
Appl. Bozitinib (PLB-1001) is a highly selective c-MET kinase inhibitor with blood-brain barrier permeability. Bozitinib (PLB-1001) is a ATP-competitive small-molecule inhibitor, binds to the conventional ATP-binding pocket of the tyrosine kinase superfamily[1].
Host
Item no.
Amount 100 mg
Available
PLB-­1001 Login PLB-1001
Type Chemicals
Clone
Specific against Other
Appl. Bozitinib (PLB-1001) is a highly selective c-MET kinase inhibitor with blood-brain barrier permeability. Bozitinib (PLB-1001) is a ATP-competitive small-molecule inhibitor, binds to the conventional ATP-binding pocket of the tyrosine kinase superfamily[1].
Host
Item no.
Amount 250 mg
Available
PLB-­1001 Login PLB-1001
Type Chemicals
Clone
Specific against Other
Appl. Bozitinib (PLB-1001) is a highly selective c-MET kinase inhibitor with blood-brain barrier permeability. Bozitinib (PLB-1001) is a ATP-competitive small-molecule inhibitor, binds to the conventional ATP-binding pocket of the tyrosine kinase superfamily[1].
Host
Item no.
Amount 1 g
Available
A4250 Login A4250
Type Chemicals
Clone
Specific against Other
Appl. A4250 (A-4250, Odevixibat) is a small molecule ileal bile acid transporter (IBAT) inhibitor for the treatment of cholestatic liver diseases including progressive familial intrahepatic cholestasis and NASH..
Host
Item no.
Amount 1 g
Available
HS220 Login HS220
Type Chemicals
Clone
Specific against Other
Appl. HS220 (HS-220) is a Plasmodium-selective takinib analog that targets atypical P. falciparum protein kinase 9 (PfPK9, Kd=4.1 uM) but does not inhibit HsTAK1, decreases K63-linked ubiquitination in P. falciparum; inhibits P. berghei parasite load in HuH7 cells with EC50 of 43 uM, with no significant change on HuH7 viability; induce a unique phenotype where parasite size in hepatocytes increases.
Host
Item no.
Amount 250 mg
Available
GDC-­0214(GDC0214) Login GDC-0214(GDC0214)
Type Chemicals
Clone
Specific against Other
Appl. GDC0214 is a potent, selective inhalable and lung-restricted inhibitor of JAK1 with IC50 of 8.52 nM, displays 6.3/704/28 fold selectivity over JAK2/JAK3/TYK2.
Host
Item no.
Amount 100 mg
Available
GDC-­0214(GDC0214) Login GDC-0214(GDC0214)
Type Chemicals
Clone
Specific against Other
Appl. GDC0214 is a potent, selective inhalable and lung-restricted inhibitor of JAK1 with IC50 of 8.52 nM, displays 6.3/704/28 fold selectivity over JAK2/JAK3/TYK2.
Host
Item no.
Amount 250 mg
Available
GDC-­0214(GDC0214) Login GDC-0214(GDC0214)
Type Chemicals
Clone
Specific against Other
Appl. GDC0214 is a potent, selective inhalable and lung-restricted inhibitor of JAK1 with IC50 of 8.52 nM, displays 6.3/704/28 fold selectivity over JAK2/JAK3/TYK2.
Host
Item no.
Amount 1 g
Available
iGOT1-­01 Login iGOT1-01
Type Chemicals
Clone
Specific against Other
Appl. iGOT1-01 is a small molecule inhibitor of aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1 (GOT1)) with IC50 of 11.3 uM.
Host
Item no.
Amount 100 mg
Available
GLP-­1(7-­36), amide Login GLP-1(7-36), amide
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 25 mg
Available
iGOT1-­01 Login iGOT1-01
Type Chemicals
Clone
Specific against Other
Appl. iGOT1-01 is a small molecule inhibitor of aspartate aminotransferase 1 (glutamate oxaloacetate transaminase 1 (GOT1)) with IC50 of 11.3 uM.
Host
Item no.
Amount 1 g
Available
YTX-­465 Login YTX-465
Type Chemicals
Clone
Specific against Other
Appl. YTX-465 (YTX465) is a specific small molecule that rescues yeast from a-Syn cytotoxicity with EC50 of 15 nM, via inhibiting Ole1, the yeast homolog of human stearoyl-CoA desaturase (SCD).
Host
Item no.
Amount 100 mg
Available
YTX-­465 Login YTX-465
Type Chemicals
Clone
Specific against Other
Appl. YTX-465 (YTX465) is a specific small molecule that rescues yeast from a-Syn cytotoxicity with EC50 of 15 nM, via inhibiting Ole1, the yeast homolog of human stearoyl-CoA desaturase (SCD).
Host
Item no.
Amount 250 mg
Available
Flupenthixol dihydrochloride Login Flupenthixol dihydrochloride
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available
Flupenthixol dihydrochloride Login Flupenthixol dihydrochloride
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 250 mg
Available
5-­R-­Rivaroxaban Login 5-R-Rivaroxaban
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 10 mg
Available
17-­AAG Login 17-AAG
Type Chemicals
Clone
Specific against Other
Appl.
Host
Item no.
Amount 100 mg
Available

1437732 Item(s)

per page

Page:
  1. 7
  2. 8
  3. 9
  4. 10
  5. 11
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