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Pesticide Std Alachlor in 1000ug/mL in MeOH
REPET104
Scientific Laboratory Supplies 1ML
BMX-IN-1
A3260-10
ApexBio 10 mg
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
BMX-IN-1
A3260-100
ApexBio 100 mg
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
BMX-IN-1
A3260-2
ApexBio 2 mg
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
BMX-IN-1
A3260-5
ApexBio 5 mg
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
BMX-IN-1
A3260-5.1
ApexBio 10 mM (in 1mL DMSO)
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
BMX-IN-1
A3260-50
ApexBio 50 mg
Description: BMX-IN-1 is a highly selective and irreversible inhibitor of BMX kinase [1].BMX, also known as ETK, is a member of Tec family and plays an important role in regulating ischemia-mediated arteriogenesis and lymphangiogenesis
JNK-IN-7
A3519-10
ApexBio 10 mg
Description: JNK-IN-7 is a selective JNK inhibitor with IC50 values of 1.54 nM, 1.99 nM, 0.75 nM to JNK1, JNK2, JNK3, respectively. It also inhibits phosphorylation of c-Jun, which is a direct substrate of JNK kinase.
JNK-IN-7
A3519-100
ApexBio 100 mg
Description: JNK-IN-7 is a selective JNK inhibitor with IC50 values of 1.54 nM, 1.99 nM, 0.75 nM to JNK1, JNK2, JNK3, respectively. It also inhibits phosphorylation of c-Jun, which is a direct substrate of JNK kinase.
JNK-IN-7
A3519-5
ApexBio 5 mg
Description: JNK-IN-7 is a selective JNK inhibitor with IC50 values of 1.54 nM, 1.99 nM, 0.75 nM to JNK1, JNK2, JNK3, respectively. It also inhibits phosphorylation of c-Jun, which is a direct substrate of JNK kinase.
JNK-IN-7
A3519-5.1
ApexBio 10 mM (in 1mL DMSO)
Description: JNK-IN-7 is a selective JNK inhibitor with IC50 values of 1.54 nM, 1.99 nM, 0.75 nM to JNK1, JNK2, JNK3, respectively. It also inhibits phosphorylation of c-Jun, which is a direct substrate of JNK kinase.
JNK-IN-7
A3519-50
ApexBio 50 mg
Description: JNK-IN-7 is a selective JNK inhibitor with IC50 values of 1.54 nM, 1.99 nM, 0.75 nM to JNK1, JNK2, JNK3, respectively. It also inhibits phosphorylation of c-Jun, which is a direct substrate of JNK kinase.
JNK-IN-8
A3520-10
ApexBio 10 mg
Description: JNK-IN-8 is a specific JNK1/2/3 inhibitor with IC50 value of 4.67, 18.7, 0.98 nM respectively [1].
JNK-IN-8
A3520-5
ApexBio 5 mg
Description: JNK-IN-8 is a specific JNK1/2/3 inhibitor with IC50 value of 4.67, 18.7, 0.98 nM respectively [1].
JNK-IN-8
A3520-5.1
ApexBio 10 mM (in 1mL DMSO)
Description: JNK-IN-8 is a specific JNK1/2/3 inhibitor with IC50 value of 4.67, 18.7, 0.98 nM respectively [1].
JNK-IN-8
A3520-50
ApexBio 50 mg
Description: JNK-IN-8 is a specific JNK1/2/3 inhibitor with IC50 value of 4.67, 18.7, 0.98 nM respectively [1].
LRRK2-IN-1
A3558-10
ApexBio 10 mg
Description: LRRK2-IN-1 is a potent and selective inhibitor of LRRK2 with IC50 value of 13 nM. [1]LRRK2 (Leucine-rich repeat kinase 2) is also known dardarin. LRRK2 belongs to the leucine-rich repeat kinase family.
LRRK2-IN-1
A3558-100
ApexBio 100 mg
Description: LRRK2-IN-1 is a potent and selective inhibitor of LRRK2 with IC50 value of 13 nM. [1]LRRK2 (Leucine-rich repeat kinase 2) is also known dardarin. LRRK2 belongs to the leucine-rich repeat kinase family.
LRRK2-IN-1
A3558-5.1
ApexBio 10 mM (in 1mL DMSO)
Description: LRRK2-IN-1 is a potent and selective inhibitor of LRRK2 with IC50 value of 13 nM. [1]LRRK2 (Leucine-rich repeat kinase 2) is also known dardarin. LRRK2 belongs to the leucine-rich repeat kinase family.
LRRK2-IN-1
A3558-50
ApexBio 50 mg
Description: LRRK2-IN-1 is a potent and selective inhibitor of LRRK2 with IC50 value of 13 nM. [1]LRRK2 (Leucine-rich repeat kinase 2) is also known dardarin. LRRK2 belongs to the leucine-rich repeat kinase family.
Jnk-In-7
20-abx184143
Abbexa
  • 10 mg
  • 5 mg
TMPRSS2 (IN) Antibody
9571-002mg
ProSci 0.02 mg
Description: TMPRSS2 Antibody: TMPRSS2 is a plasma membrane-anchored serine protease that participates in proteolytic cascades of relevance for the normal physiologic function of the prostate. Androgen-induced TMPRSS2 activates several substrates that include pro-hepatocyte growth factor/HGF, the protease activated receptor-2/F2RL1 or matriptase/ST14 leading to extracellular matrix disruption and metastasis of prostate cancer cells. It facilitates human coronaviruses SARS-CoV and SARS-CoV-2 infections via two independent mechanisms, proteolytic cleavage of ACE2 receptor which promotes viral uptake, and cleavage of coronavirus spike glycoproteins which activates the glycoprotein for host cell entry. It proteolytically cleaves and activates the spike glycoproteins of human coronavirus 229E (HCoV-229E) and human coronavirus EMC (HCoV-EMC) and the fusion glycoproteins F0 of Sendai virus (SeV), human metapneumovirus (HMPV), human parainfluenza 1, 2, 3, 4a and 4b viruses (HPIV). TMPRSS2 is essential for spread and pathogenesis of influenza A virus (strains H1N1, H3N2 and H7N9), and it is involved in proteolytic cleavage and activation of hemagglutinin (HA) protein which is essential for viral infectivity.
TMPRSS2 (IN) Antibody
9571-01mg
ProSci 0.1 mg
Description: TMPRSS2 Antibody: TMPRSS2 is a plasma membrane-anchored serine protease that participates in proteolytic cascades of relevance for the normal physiologic function of the prostate. Androgen-induced TMPRSS2 activates several substrates that include pro-hepatocyte growth factor/HGF, the protease activated receptor-2/F2RL1 or matriptase/ST14 leading to extracellular matrix disruption and metastasis of prostate cancer cells. It facilitates human coronaviruses SARS-CoV and SARS-CoV-2 infections via two independent mechanisms, proteolytic cleavage of ACE2 receptor which promotes viral uptake, and cleavage of coronavirus spike glycoproteins which activates the glycoprotein for host cell entry. It proteolytically cleaves and activates the spike glycoproteins of human coronavirus 229E (HCoV-229E) and human coronavirus EMC (HCoV-EMC) and the fusion glycoproteins F0 of Sendai virus (SeV), human metapneumovirus (HMPV), human parainfluenza 1, 2, 3, 4a and 4b viruses (HPIV). TMPRSS2 is essential for spread and pathogenesis of influenza A virus (strains H1N1, H3N2 and H7N9), and it is involved in proteolytic cleavage and activation of hemagglutinin (HA) protein which is essential for viral infectivity.
TMPRSS2 (IN) Peptide
9571P
ProSci 0.05 mg
Description: TMPRSS2 (IN)
Mps1-IN-2
B1138-25
ApexBio 25 mg
Description: Mps1-IN-2 is a potent and selective ATP-competitive inhibitor of Mps1 kinase with the IC50 value of 145nM [1].Mps1-IN-2 has been reported to inhibit Mps1 kinase activity with the IC50 value of 145nM, when screened at 1?M ATP.
Mps1-IN-2
B1138-5
ApexBio 5 mg
Description: Mps1-IN-2 is a potent and selective ATP-competitive inhibitor of Mps1 kinase with the IC50 value of 145nM [1].Mps1-IN-2 has been reported to inhibit Mps1 kinase activity with the IC50 value of 145nM, when screened at 1?M ATP.
Kif15-IN-1
B3280-10
ApexBio 10 mg
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-1
B3280-100
ApexBio 100 mg
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-1
B3280-1000
ApexBio 1 g
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-1
B3280-5
ApexBio 5 mg
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-1
B3280-50
ApexBio 50 mg
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-1
B3280-S
ApexBio Evaluation Sample
Description: Kif15-IN-1, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-2
B3281-10
ApexBio 10 mg
Description: Kif15-IN-2, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-2
B3281-100
ApexBio 100 mg
Description: Kif15-IN-2, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-2
B3281-5
ApexBio 5 mg
Description: Kif15-IN-2, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
Kif15-IN-2
B3281-50
ApexBio 50 mg
Description: Kif15-IN-2, a potent Kif15 kinesin inhibitor; inhibits cellular proliferation in various tumor cell lines [1].Kif15,also known as Kinesin-12 and HKLP2, is a motor protein expressed in all cells during mitosis and in postmitotic neurons undergoing axon growth [2].
DDR1-IN-1
B3383-10
ApexBio 10 mg
Description: DDR1-IN-1 is a potent and selective DDR1 receptor tyrosine kinase inhibitor with IC50/EC50 of 105 nM/87 nM; 4-fold less potent for DDR2 (IC50= 413 nM).
DDR1-IN-1
B3383-5
ApexBio 5 mg
Description: DDR1-IN-1 is a potent and selective DDR1 receptor tyrosine kinase inhibitor with IC50/EC50 of 105 nM/87 nM; 4-fold less potent for DDR2 (IC50= 413 nM).
DUBs-IN-2
B3515-10
ApexBio 10 mg
Description: IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.
DUBs-IN-2
B3515-100
ApexBio 100 mg
Description: IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.
DUBs-IN-2
B3515-5
ApexBio 5 mg
Description: IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.
DUBs-IN-2
B3515-5.1
ApexBio 10 mM (in 1mL DMSO)
Description: IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.
DUBs-IN-2
B3515-50
ApexBio 50 mg
Description: IC50s: 7.2 M/0.93 M for USP7/USP8, respectively.DUBs-IN-2 is a potent deubiquitinase enzyme inhibitor.
DUBs-IN-3
B3516-10
ApexBio 10 mg
DUBs-IN-3
B3516-100
ApexBio 100 mg
DUBs-IN-3
B3516-5
ApexBio 5 mg
DUBs-IN-3
B3516-50
ApexBio 50 mg
CDK7-IN-1
B4665-1
ApexBio 1 mg
IKK?-IN-1
B4825-10
ApexBio 10 mg
IKK?-IN-1
B4825-100
ApexBio 100 mg
IKK?-IN-1
B4825-5
ApexBio 5 mg
IKK?-IN-1
B4825-5.1
ApexBio 10 mM (in 1mL DMSO)
IKK?-IN-1
B4825-50
ApexBio 50 mg
Mps1-IN-1
B4907-10
ApexBio 10 mg
Description: Mps1-IN-1 is a selective Mps1 (monopolar spindle 1) kinase inhibitor with IC50 value of 367 nM.MPS1 (monopolar spindle 1 kinase) is a crucial part of the spindle assembly checkpoint.
Mps1-IN-1
B4907-5
ApexBio 5 mg
Description: Mps1-IN-1 is a selective Mps1 (monopolar spindle 1) kinase inhibitor with IC50 value of 367 nM.MPS1 (monopolar spindle 1 kinase) is a crucial part of the spindle assembly checkpoint.
Mps1-IN-1
B4907-5.1
ApexBio 10 mM (in 1mL DMSO)
Description: Mps1-IN-1 is a selective Mps1 (monopolar spindle 1) kinase inhibitor with IC50 value of 367 nM.MPS1 (monopolar spindle 1 kinase) is a crucial part of the spindle assembly checkpoint.
Mps1-IN-1
B4907-50
ApexBio 50 mg
Description: Mps1-IN-1 is a selective Mps1 (monopolar spindle 1) kinase inhibitor with IC50 value of 367 nM.MPS1 (monopolar spindle 1 kinase) is a crucial part of the spindle assembly checkpoint.
IDO-IN-1
C3211-1
ApexBio 1 mg
Description: IC50: 59 nMIDO-IN-1 is an indoleamine-2,3-dioxygenase (IDO) inhibitor.
IDO-IN-1
C3211-10
ApexBio 10 mg
Description: IC50: 59 nMIDO-IN-1 is an indoleamine-2,3-dioxygenase (IDO) inhibitor.
IDO-IN-1
C3211-5
ApexBio 5 mg
Description: IC50: 59 nMIDO-IN-1 is an indoleamine-2,3-dioxygenase (IDO) inhibitor.
IKK-IN-1
HY-13873
MedChemExpress 1mg
PKR-IN-C16
HY-13977A
MedChemExpress 10mM/1mL
DDR1-IN-1
HY-13979
MedChemExpress 100mg
IDO-IN-7
HY-13983
MedChemExpress 10mM/1mL
Mps1-IN-2
HY-13994
MedChemExpress 100mg
ERK5-IN-1
HY-14403
MedChemExpress 100mg
JNK-IN-7
HY-15617
MedChemExpress 10mM/1mL
MIR96-IN-1
HY-15843
MedChemExpress 10mg
Kif15-IN-1
HY-15948
MedChemExpress 10mg
Kif15-IN-2
HY-15949
MedChemExpress 100mg
CDK9-IN-2
HY-16462
MedChemExpress 50mg
Mcl1-IN-1
HY-16669
MedChemExpress 100mg
USP7-IN-1
HY-16709
MedChemExpress 100mg
PKC-IN-1
HY-16903
MedChemExpress 10mM/1mL
IDO-IN-3
HY-16987
MedChemExpress 2mg
CaMKII-IN-1
HY-18271
MedChemExpress 10mM/1mL
AKT-IN-1
HY-18296
MedChemExpress 5mg
Chitinase-IN-1
HY-18598
MedChemExpress 10mM/1mL
Chitinase-IN-2
HY-18599
MedChemExpress 10mg
BoNT-IN-1
HY-18671
MedChemExpress 10mg
ILK-IN-2
HY-18676B
MedChemExpress 2mg
FLT3-IN-2
HY-18744
MedChemExpress 10mM/1mL
IDO-IN-4
HY-18769
MedChemExpress 50mg
IDO-IN-5
HY-18770
MedChemExpress 10mg
IDO-IN-6
HY-18770A
MedChemExpress 10mg
IDO-IN-8
HY-18770C
MedChemExpress 10mg
MAPK13-IN-1
HY-18850
MedChemExpress 10mM/1mL
RIPK1-IN-4
HY-18901
MedChemExpress 25mg
Nav1.7-IN-2
HY-19366
MedChemExpress 10mM/1mL
JAK3-IN-1
HY-19544
MedChemExpress 100mg
PKR-IN-2
HY-19702
MedChemExpress 100mg
BET-IN-1
HY-19760
MedChemExpress 10mM/1mL
HDAC-IN-3
HY-19772
MedChemExpress 50mg
PI4KIIIbeta-IN-9
HY-19798
MedChemExpress 50mg
EGFR-IN-3
HY-19815
MedChemExpress 100mg
HSL-IN-3
HY-23524
MedChemExpress 1mg
DUBs-IN-1
HY-50736
MedChemExpress 10mM/1mL
DUBs-IN-3
HY-50737
MedChemExpress 50mg
DUBs-IN-2
HY-50737A
MedChemExpress 5mg
FAAH-IN-2
HY-79511
MedChemExpress 5g

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