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T6796CB-5083Inhibitor,inhibit,multiple,p97,VCP,solid,tumors,myeloma,AAA,ATPase,Cdc48,CB-5083
CB-5083 is a potent, selective, and orally bioavailable p97 AAA ATPase inhibitor ( IC50=11 nM).
价 格：￥电议型 号：T6796产 地：中国大陆
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T1782CanagliflozinJNJ 28431754AAA；TA 7284；JNJ 28431754；JNJ 24831754ZAE；卡格列净
Canagliflozin, a sodium-glucose transporter 2( SGLT2) and P-Glycoprotein inhibitor, is used in type 2 diabetes.
价 格：￥电议型 号：T1782产 地：中国大陆
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T1782CanagliflozinCanagliflozin,JNJ 28431754,JNJ 28431754AAA
Canagliflozin, a sodium-glucose transporter 2( SGLT2) and P-Glycoprotein inhibitor, is used in type 2 diabetes.
价 格：￥电议型 号：T1782产 地：美洲
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T63834AAK1-IN-3 TFA；化合物 AAK1-IN-3 TFAAAK1-IN-3 TFA
AAK1-IN-3 TFA is an adaptor protein 2-associated kinase 1 (AAK1) inhibitor (IC50: 11 nM) that crosses the blood-brain barrier and is a quinoline analogue.AAK1-IN-3 has shown potential for research in neuropathic pain.
价 格：￥电议型 号：T63834产 地：中国大陆
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T63833AAK1-IN-2 TFA；化合物 AAK1-IN-2 TFAAAK1-IN-2 TFA
AAK1-IN-2 TFA (compound (S)-31) is a selective and potent AAK1 inhibitor (IC50: 5.8 nM) that can cross the blood-brain barrier.
价 格：￥电议型 号：T63833产 地：中国大陆
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T63616AAA-10 formic；化合物 AAA-10 formicAAA-10 formic
AAA-10 formic is an orally active inhibitor of intestinal bacterial bile salt hydrolase (BSH) against B. thetarBSH (IC50: 10 nM) and B. longumrBSH (IC50: 80 nM).
价 格：￥电议型 号：T63616产 地：中国大陆
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T63060AAA-10；化合物 AAA-10AAA-10
AAA-10 is an orally active inhibitor of bile salt hydrolase (BSH) in B. intestinalis that acts on B. thetarBSH (IC50: 10 nM) and B. longumrBSH (IC50: 80 nM).
价 格：￥电议型 号：T63060产 地：中国大陆
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T60767NAAA-IN-1；化合物 NAAA-IN-1NAAA-IN-1
NAAA-IN-1 (Compound 1) can be used in the inflammation and pain research. NAAA-IN-1 is a potent and selective NAAA inhibitor (IC 50 = 7 nM). NAAA is a cysteine amidase. NAAA preferentially hydrolyzes the endogenous biolipids palmitoylethanolamide (PEA) and oleoylethanolamide (OEA) [1].
价 格：￥电议型 号：T60767产 地：中国大陆
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T60432NAAA-IN-3；化合物 NAAA-IN-3NAAA-IN-3
NAAA-IN-3 (Compound 17a) is a potent and selective NAAA inhibitor with an IC50 of 50 nM. NAAA is a cysteine amidase which preferentially hydrolyzes the endogenous biolipids palmitoylethanolamide (PEA) and oleoylethanolamide (OEA). PEA is an endogenous agonist of the nuclear peroxisome proliferator-activated receptor-α (PPAR-α), which is a key regulator of inflammation and pain. The potential role of NAAA-IN-3 is as a therapeutic agent for the treatment of inflammation and pain.
价 格：￥电议型 号：T60432产 地：中国大陆
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T60378NAAA-IN-2；化合物 NAAA-IN-2NAAA-IN-2
NAAA-IN-2 (Compound 9), a potent and selective inhibitor of NAAA, exhibits an IC50 of 50 nM. NAAA, a cysteine amidase, primarily breaks down the endogenous biolipids palmitoylethanolamide (PEA) and oleoylethanolamide (OEA). This compound demonstrates promise for inflammation and pain research [1].
价 格：￥电议型 号：T60378产 地：中国大陆
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T40049MC-AAA-NHCH2OCH2COO-7-aminomethyl-10-methyl-11-fluoro camptothecin；MC-AAA-NHCH2OCH2COO-7-aminomethyl
MC-AAA-NHCH2OCH2COO-7-aminomethyl-10-methyl-11-fluoro camptothecin (compound 21a), is a camptothecin payload which can be utilized in the synthesis of a camptothecin antibody-drug conjugate (ADC) by conjugation to a monoclonal antibody (mAb).
价 格：￥电议型 号：T40049产 地：中国大陆
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T40048MC-AAA-NHCH2OCH2COOH；MC-AAA-NHCH2OCH2COOHMC-AAA-NHCH2OCH2COOH；MC-AAA-NHCH2OCH2COOH
MC-AAA-NHCH2OCH2COOH (compound 20) is a cleavable antibody-drug conjugate (ADC) linker. Its primary application lies in the synthesis of ADCs.
价 格：￥电议型 号：T40048产 地：中国大陆
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T35855AAA；AAAAAA
AAA is an antagonist of G protein-coupled receptor 75 (GPR75).1It increases basal GPR75 protein levels and inhibits 20-HETE-induced reductions in GPR75 protein levels in PC3 cells. AAA (5 and 10 μM) also reduces 20-HETE-induced phosphorylation of EGFR, NF-κB, and Akt in, and cell migration of, PC3 cells.
价 格：￥电议型 号：T35855产 地：中国大陆
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T2S1115Albaspidin AA；白绵马素AAAlbaspidin AA
Albaspidin AA displays strong antibacterial activity against the vegetative form of P. larvae (MIC ranging from 0.168-220 uM). It may have in vitro nematocidal activity against L4 stage larvae.
价 格：￥电议型 号：T2S1115产 地：中国大陆
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T1782Canagliflozin；卡格列净JNJ 24831754ZAE|||JNJ 28431754AAA|||TA 7284|||JNJ 28431754；卡格列净|||JNJ 24831754ZAE|
Canagliflozin (JNJ 28431754AAA), a sodium-glucose transporter 2( SGLT2) and P-Glycoprotein inhibitor, is used in type 2 diabetes.
价 格：￥电议型 号：T1782产 地：中国大陆
