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T2648Pimecrolimus吡美莫司；SDZ-ASM 981；ASM 981
Pimecrolimus, a calcineurin inhibitor immunosuppressant, binds to the receptor macrophilin-12 (FKBP-12) forming a complex that blocks the calcium-dependent signal transduction cascade mediated by calcineurin.
价 格：￥电议型 号：T2648产 地：中国大陆
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T24134HDL376HDL-376；SDZ HDL376；SDZ-HDL376；HDL 376；SDZHDL376
HDL376 is a scavenger receptor BI inhibitor.
价 格：￥电议型 号：T24134产 地：中国大陆
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T1784EverolimusRAD001；SDZ-RAD；依维莫司
Everolimus is a potent mTOR inhibitor that binds to FKBP-12. It is used alone or in combination with calcineurin inhibitors.
价 格：￥电议型 号：T1784产 地：中国大陆
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T1628Rivastigmine tartrate酒石酸卡巴拉汀；ENA 713；SDZ-ENA 713
Rivastigmine tartrate is a carbamate-derived reversible CHOLINESTERASE INHIBITOR that is selective for the CENTRAL NERVOUS SYSTEM and is used for the treatment of DEMENTIA in ALZHEIMER DISEASE and PARKINSON DISEASE.
价 格：￥电议型 号：T1628产 地：中国大陆
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T1551Tegaserod maleateSDZ-HTF-919；HTF-919；马来酸替加色罗
Tegaserod is a 5-HT4 agonist manufactured by Novartis and used for the management of irritable bowel syndrome and constipation. Its use was the only drug approved by the United States Food and Drug Administration to help relieve the abdominal discomfort,
价 格：￥电议型 号：T1551产 地：中国大陆
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T1173Tropisetron hydrochlorideSDZ-ICS 930；ICS 205-930；Tropisetron HCl；盐酸托烷司琼
Tropisetron Hydrochloride is the hydrochloride salt form of tropisetron, a selective, competitive serotonin 5-hydroxytryptamine type 3 (5-HT3) receptor antagonist, with antinauseant and antiemetic activities.
价 格：￥电议型 号：T1173产 地：中国大陆
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T0229Rivastigmine卡巴拉汀；利凡斯的明；SDZ-ENA 713；S-Rivastigmine；Exelon
Rivastigmine is a Cholinesterase Inhibitor, used for therapy of Alzheimer disease.
价 格：￥电议型 号：T0229产 地：中国大陆
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T0229RivastigmineRivastigmine,S-Rivastigmine,SDZ-ENA 713
Rivastigmine is a Cholinesterase Inhibitor, used for therapy of Alzheimer disease.
价 格：￥电议型 号：T0229产 地：美洲
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T1173Tropisetron hydrochlorideTropisetron hydrochloride,SDZ-ICS 930,Tropisetron HCl
Tropisetron Hydrochloride is the hydrochloride salt form of tropisetron, a selective, competitive serotonin 5-hydroxytryptamine type 3 (5-HT3) receptor antagonist, with antinauseant and antiemetic activities.
价 格：￥电议型 号：T1173产 地：美洲
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T12226NIM811NIM811,(Melle-4)cyclosporin,SDZ NIM811
NIM811 is an orally bioavailable dual inhibitor of mitochondrial permeability transition and cyclophilin.
价 格：￥电议型 号：T12226产 地：美洲
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T12872SDZ 220-581 Ammonium saltSDZ 220-581 Ammonium salt
SDZ 220-581 Ammonium salt is a potent, orally active and competitive antagonist of NMDA receptor(pKi : 7.7).
价 格：￥电议型 号：T12872产 地：美洲
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T12873SDZ-MKS 492SDZ-MKS 492,MKS 492,
SDZ-MKS 492 is a selective type III isozyme cyclic nucleotide phosphodiesterase inhibitor.
价 格：￥电议型 号：T12873产 地：美洲
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T12889SDZ 220-581SDZ 220-581
SDZ 220-581 is a potent, orally active and competitive antagonist of NMDA receptor(pKi : 7.7).
价 格：￥电议型 号：T12889产 地：美洲
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T1551Tegaserod maleateTegaserod maleate,HTF-919,SDZ-HTF-919
Tegaserod is a 5-HT4 agonist manufactured by Novartis and used for the management of irritable bowel syndrome and constipation. Its use was the only drug approved by the United States Food and Drug Administration to help relieve the abdominal discomfort,
价 格：￥电议型 号：T1551产 地：美洲
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T1628Rivastigmine tartrateRivastigmine tartrate,SDZ-ENA 713,ENA 713
Rivastigmine tartrate is a carbamate-derived reversible CHOLINESTERASE INHIBITOR that is selective for the CENTRAL NERVOUS SYSTEM and is used for the treatment of DEMENTIA in ALZHEIMER DISEASE and PARKINSON DISEASE.
价 格：￥电议型 号：T1628产 地：美洲
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T1784EverolimusEverolimus,SDZ-RAD,RAD001
Everolimus is a potent mTOR inhibitor that binds to FKBP-12. It is used alone or in combination with calcineurin inhibitors.
价 格：￥电议型 号：T1784产 地：美洲
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T2648PimecrolimusPimecrolimus,SDZ-ASM 981,ASM 981
Pimecrolimus, a calcineurin inhibitor immunosuppressant, binds to the receptor macrophilin-12 (FKBP-12) forming a complex that blocks the calcium-dependent signal transduction cascade mediated by calcineurin.
价 格：￥电议型 号：T2648产 地：美洲
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T71466Sdz 210-096；化合物 Sdz 210-096Sdz 210-096
Sdz 210-096 is a novel opiate antagonist. It is a novel 14 beta-benzyl morphinan derivative with antagonistic actions at mu and kappa opiate receptors. This compound has been characterized for luteinizing hormone (LH) secretion-stimulating effects in a variety of experimental paradigms in the rat.
价 格：￥电议型 号：T71466产 地：中国大陆
