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T9374AA38-3serine,ABHD6,Fatty acid amide hydrolase,AA38 3,Monoacylglycerol lipase,AA383,ABHD11,FAAH,MAGL,
AA38-3 inhibites three SHs (ABHD6, ABHD11, and FAAH)
价 格：￥电议型 号：T9374产 地：中国大陆
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T63536Dual FAAH/sEH-IN-1
Dual FAAH/sEH-IN-1 is a dual inhibitor of sEH (soluble epoxide hydrolase) (IC50: 9.6 nM) and FAAH (fatty acid amide hydrolase) (IC50: 7 nM) with high affinity and anti-inflammatory activity.
价 格：￥电议型 号：T63536产 地：中国大陆
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T8927WWL 154FAAH-4,Fatty acid amide hydrolase,Inhibitor,inhibit,WWL154,JZL184,WWL 154,FAAH
WWL 154 is an serine hydrolase (SH) and fatty acid amide hydrolase FAAH-4 inhibitor.
价 格：￥电议型 号：T8927产 地：中国大陆
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T67747CB2R/FAAH modulator-3CB2R/FAAHmodulator3
CB2R/FAAH modulator-3 (compound 27) is a modulator targeting at CB2R and FAAH. CB2R/FAAH modulator-3 acts as a CB2R agonist and FAAH inhibitor, the Ki values are 20.1 and 67.6 nM for CB2R and CB1R, respectively, and the IC50 value for FAAH is 3.4 μM. CB2R/FAAH modulator-3 has research value related to cancer, deleterious inflammatory cascades occurring in neurodegenerative diseases, and COVID-19 infection.
价 格：￥电议型 号：T67747产 地：中国大陆
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T8646URB937FAAH,URB 937,Inhibitor,URB937,low,toxicity,inhibit,Fatty acid amide hydrolase,OEA,URB-937
URB937 is an inhibitor of FAAH and increases anandamide levels(IC50 : 26.8 nM).
价 格：￥电议型 号：T8646产 地：中国大陆
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T9967MAGL-IN-5Inhibitor,inhibit,MAGLIN5,MAGL IN 5,FAAH,Fatty acid amide hydrolase,Monoacylglycerol lipase
MAGL-IN-5 is a non-selective lipase inhibitor.
价 格：￥电议型 号：T9967产 地：中国大陆
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T67745CB2R/FAAH?modulator-2CB2R/FAAH?modulator2
CB2R/FAAH modulator-2 (compound 26) is a dual modulator targeting at CB2R and FAAH. CB2R/FAAH modulator-2 acts as a CB2R agonist and FAAH inhibitor, the Ki values are 10.8 and 152.9 nM for CB2R and CB1R, respectively, and the IC50 value for FAAH is 6.2 μM. CB2R/FAAH modulator-2 has studies research value related to cancer, deleterious inflammatory cascades occurring in neurodegenerative diseases, and COVID-19 infection.
价 格：￥电议型 号：T67745产 地：中国大陆
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T15268FAAH-IN-2O-Desmorpholinopropyl Gefitinib；4-(3-氯-4-氟苯氨基)-7-甲氧基喹唑啉-6-醇
FAAH-IN-2 is a potent inhibitor of FAAH(fatty acid amide hydrolase).
价 格：￥电议型 号：T15268产 地：中国大陆
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T11256FAAH inhibitor 1Benzothiazole analog 3
FAAH inhibitor 1 is a potent fatty acid amide hydrolase (FAAH) inhibitor with an IC50 of 18±8 nM.
价 格：￥电议型 号：T11256产 地：中国大陆
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T15268FAAH-IN-2FAAH-IN-2,O-Desmorpholinopropyl Gefitinib,
FAAH-IN-2 is a potent inhibitor of FAAH(fatty acid amide hydrolase).
价 格：￥电议型 号：T15268产 地：美洲
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T83223AaHI；化合物 AaHIAaHI
AaHI, a neurotoxin sourced from the venom of the North African scorpion Androctonus australis hector, serves as a research tool for creating agents with the ability to neutralize toxins [1].
价 格：￥电议型 号：T83223产 地：中国大陆
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T82421FAAH/cPLA2α-IN-1；化合物 FAAH/cPLA2α-IN-1FAAH/cPLA2α-IN-1
FAAH/cPLA2α-IN-1 is a compound that simultaneously inhibits both FAAH and cPLA2α, demonstrating potent activity with half-maximal inhibitory concentrations (IC50s) of 32 nM for FAAH and 47 nM for cPLA2α [1].
价 格：￥电议型 号：T82421产 地：中国大陆
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T80162Aah II；化合物 Aah IIAah II
Aah II, a sodium channel modulator, is a toxin derived from the venom of the scorpion Androctonus australis [1] [2].
价 格：￥电议型 号：T80162产 地：中国大陆
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T73302FAAH-IN-7；化合物 FAAH-IN-7FAAH-IN-7
FAAH-IN-7, a potent and reversible inhibitor of fatty acid amide hydrolase (FAAH), demonstrates significant neuroprotective effects, particularly by mitigating oxidative stress in 1321N1 astrocytes. With an IC50 value of 8.29 nM, it also shows notable efficacy in an ex vivo neuroinflammation model.
价 格：￥电议型 号：T73302产 地：中国大陆
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T67896CB2R/FAAHu00A0modulator-1；CB2R/FAAH调节剂-1CB2R/FAAHu00A0modulator-1
CB2R/FAAH?modulator-1, a cannabinoid type 2 receptor (CB2R) agonist, is also a fatty acid amide hydrolase (FAAH) inhibitor (IC50=4 μM) that reduces the production of pro-inflammatory and anti-inflammatory cytokines and is commonly used in inflammation studies. The Kis for CB2R and CB1R are 14.8 nM and 241.3 nM, respectively.
价 格：￥电议型 号：T67896产 地：中国大陆
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T67747CB2R/FAAH modulator-3；化合物CB2R/FAAH modulator-3CB2R/FAAH modulator-3
CB2R/FAAH modulator-3 (compound 27) is a modulator targeting at CB2R and FAAH. CB2R/FAAH modulator-3 acts as a CB2R agonist and FAAH inhibitor, the Ki values are 20.1 and 67.6 nM for CB2R and CB1R, respectively, and the IC50 value for FAAH is 3.4 μM. CB2R/FAAH modulator-3 has research value related to cancer, deleterious inflammatory cascades occurring in neurodegenerative diseases, and COVID-19 infection.
价 格：￥电议型 号：T67747产 地：中国大陆
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T67745CB2R/FAAHu00A0modulator-2；化合物CB2R/FAAHu00A0modulator-2CB2R/FAAHu00A0modulator-2
CB2R/FAAH modulator-2 (compound 26) is a dual modulator targeting at CB2R and FAAH. CB2R/FAAH modulator-2 acts as a CB2R agonist and FAAH inhibitor, the Ki values are 10.8 and 152.9 nM for CB2R and CB1R, respectively, and the IC50 value for FAAH is 6.2 μM. CB2R/FAAH modulator-2 has studies research value related to cancer, deleterious inflammatory cascades occurring in neurodegenerative diseases, and COVID-19 infection.
价 格：￥电议型 号：T67745产 地：中国大陆
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T6714URB-597；化合物URB597KDS-4103|||FAAH Inhibitor II；KDS-4103|||FAAH Inhibitor II
URB-597 (FAAH Inhibitor II) is an effective, orally bioavailable FAAH inhibitor (IC50: 4.6 nM), and no effect on other cannabinoid-related targets.
价 格：￥电议型 号：T6714产 地：中国大陆
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T63536Dual FAAH/sEH-IN-1；化合物Dual FAAH/sEH-IN-1Dual FAAH/sEH-IN-1
Dual FAAH/sEH-IN-1 is a dual inhibitor of sEH (soluble epoxide hydrolase) (IC50: 9.6 nM) and FAAH (fatty acid amide hydrolase) (IC50: 7 nM) with high affinity and anti-inflammatory activity.
价 格：￥电议型 号：T63536产 地：中国大陆
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T62671FAAH/MAGL-IN-3；化合物 FAAH/MAGL-IN-3FAAH/MAGL-IN-3
FAAH/MAGL-IN-3 (Compound 10) is an irreversible dual inhibitor of fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL) that acts on FAAH (IC50: 179 nM) and MAGL (IC50: 759 nM). FAAH/MAGL-IN-3 showed little PAMPA (parallel artificial membrane permeability assay) permeability.
价 格：￥电议型 号：T62671产 地：中国大陆
