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产品数：86101
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T28908TA-606；化合物 T28908TA606|||TA-606 free|||TA-606 free|||TA 606|||TA 606|||TA606|||TA-606 free|||TA-606|
TA-606 is an angiotensin type 1 receptor antagonist with antihypertensive activity.
价 格：￥电议型 号：T28908产 地：中国大陆
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T28905T-611 free base；化合物 T28905T-0902611|||T-2611|||T0902611|||T-902611|||T2611|||T-611；T-0902611|||T-261
T-611, a cytomegalovirus replication inhibitor, is used potentially for the treatment of cytomegalovirus infections.
价 格：￥电议型 号：T28905产 地：中国大陆
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T28880Sulfazecin free acid；化合物 T28880G 6302|||Antibiotic G 6302|||Sulfazecin|||Antibiotic EM 5210；G 6302||
Sulfazecin is a β-Lactam antibiotic.
价 格：￥电议型 号：T28880产 地：中国大陆
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T28857SSR-182289A (Free)；化合物 T28857SSR182289|||SSR-182289A|||SSR-182289|||SSR 182289A|||SSR182289A|||SSR 1
SSR-182289A (Free) is a thrombin inhibitor.
价 格：￥电议型 号：T28857产 地：中国大陆
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T28851SRA880 free base；化合物 T28851SRA 880|||NVPSRA880|||NVP SRA880|||NVP-SRA880|||SRA-880|||SRA880；SRA 880|
SRA880 is a non-peptide antagonist of somatostatin sst1-receptor. SRA880 displayed significantly lower affinity for the other human recombinant somatostatin receptors ( pK(d) < or = 6.0). SRA880 shows a certain binding affinity to the human dopamine D4 receptors. SRA880 positively modulates release of endogenous SRIF, was found to synergize with imipramine in causing antidepressant-like effects in the tail suspension test.
价 格：￥电议型 号：T28851产 地：中国大陆
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T28814SM19712 free acid；化合物 T28814SM 19712|||SM-19712|||SM19712；SM 19712|||SM-19712|||SM19712
SM19712 free acid is an inhibitor of nonpeptide endothelin converting enzyme.
价 格：￥电议型 号：T28814产 地：中国大陆
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T28782Sinoporphyrin sodium；化合物 T28782sinoporphyrin|||DVDMS Free|||DVDMS；sinoporphyrin|||DVDMS Free|||DVDMS
Sinoporphyrin sodium significantly suppressed cell proliferation, promoted early apoptotic response, triggered collapse of F-actin filaments and inhibited cell migration. Sinoporphyrin sodium potentially a treatment for cancer. Sinoporphyrin sodium is also a photosensitizer.
价 格：￥电议型 号：T28782产 地：中国大陆
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T28729SCH-50910 free base；化合物 T28729SCH50910|||SCH 50910；SCH50910|||SCH 50910
SCH-50910 is an antagonist of GABAB receptor.
价 格：￥电议型 号：T28729产 地：中国大陆
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T28694SB-743921 free base；化合物 T28694SB743921|||SB-921|||SB921|||SB-743921|||GSK-743921|||GSK-921；SB743921|
SB-743921, a kinesin spindle protein (KSP) inhibitor, is used potentially for the treatment of non-Hodgkin´s lymphoma (NHL).
价 格：￥电议型 号：T28694产 地：中国大陆
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T28661Sarecycline free base化合物Sarecycline free baseWC3035|||P 005672|||P005672|||WC 3035|||WC-3035|||P-005
Sarecycline free base (P005672) is a tetracycline-derived, narrow-spectrum antibiotic.
价 格：￥电议型 号：T28661产 地：中国大陆
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T28614RPC425 free base；化合物 T28614RPC425|||RPC-425|||RPC 425；RPC425|||RPC-425|||RPC 425
RPC425 is a noncompetitive inhibitors of the Betaine-γ-Aminobutyric Acid Transporter 1 (BGT1).
价 格：￥电议型 号：T28614产 地：中国大陆
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T28508RDEA-806 free acid；化合物 T28508VRX-806|||VRX 806|||RDEA-806|||AR 806|||AR-806|||RDEA 806；VRX-806|||VRX
RDEA-806, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.
价 格：￥电议型 号：T28508产 地：中国大陆
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T28498Lrac-CCT-250863 HCl；化合物rac-CCT-250863盐酸盐rac-CCT-250863 HCl(1364269-06-6 Free base)；rac-CCT-250863 HCl
rac-CCT-250863 HCl is a selective and reversible inhibitor of NEK 2. rac-CCT-250863 HCl induces cell cycle arrest and has good anti-proliferative activity against cancer cells. rac-CCT-250863 HCl can be used in combination with Pomalidomide to induce apoptosis and can be used in combined anti-cancer studies.
价 格：￥电议型 号：T28498L产 地：中国大陆
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T28453LPropiram fumarate HCl；富马酸丙吡胺盐酸盐Propiram fumarate HCl(15686-91-6 Free base)；Propiram fumarate HCl(156
Propiram fumarate HClis an orally available Opioid receptors agonist with analgesic activity for the study of musculoskeletal pain.
价 格：￥电议型 号：T28453L产 地：中国大陆
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T28437LPomisartan 2HCl；泊米沙坦盐酸盐Pomisartan 2HCl(144702-17-0 Free base)|||BIBR363 2HCL；Pomisartan 2HCl(144702-
Pomisartan 2HCl (BIBR363 2HCL) is a small molecule AT1R antagonist used to study heart failure and hypertension.
价 格：￥电议型 号：T28437L产 地：中国大陆
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T28422Pirlindole free base；化合物 T28422Pirlindole|||Pyrazidol；Pirlindole|||Pyrazidol
Pirlindole is a reversible inhibitor of monoamine oxidase A (RIMA). It is structurally and pharmacologically related to metralindole.
价 格：￥电议型 号：T28422产 地：中国大陆
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T28388PF-5274857 mseylate (1373615-35-0 free base)；化合物 T28388PF5274857 HCl|||PF 5274857|||PF-5274857|||PF-
PF-5274857 is a potent, orally active and selective inhibitor of hedgehog (Hh) signaling pathway (IC50 = 5.8 nM, Ki = 4.6 nM) . PF-5274857 effectively penetrates the blood-brain barrier and inhibits Smo activity in the brain of primary medulloblastoma mice, resulting in improved animal survival rates.
价 格：￥电议型 号：T28388产 地：中国大陆
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T28290Pactimibe帕替麦布CS 505|||CS-505|||CS505|||Pactimibe free base|||帕替麦布
Pactimibe is a ACAT inhibitor. It has anti-atherosclerotic activity.
价 格：￥电议型 号：T28290产 地：中国大陆
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T28273LOT-551 HCl；OT-551盐酸盐OT-551 HCl（627085-11-4 Free base）；OT-551 HCl（627085-11-4 Free base）
OT-551 HCl is an NF-Κb inhibitor, a disubstituted hydroxylamine with antioxidant properties can be used for the treatment of cataracts and age-related macular degeneration and geographic atrophy (GA).
价 格：￥电议型 号：T28273L产 地：中国大陆
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T28269ORY-1001 free base；化合物 T28269RG 6016|||ORY-1001|||ORY 1001|||ORY1001|||RG-6016|||RG6016；RG 6016|||OR
ORY-1001 is a KDM1A inhibitor (IC50 <20nM) with high selectivity against related FAD dependent aminoxidases (MAO-A/B, IL4I1, KDM1B >100uM, SMOX 7uM). Treatment of THP-1 (MLL-AF9) cells with ORY-1001, results in a time/dose dependent me2H3K4 accumulation at KDM1A target genes and concomitant induction of differentiation markers (EC50 me2H3K4 and FACS CD11b <1nM). ORY-1001 induces apoptosis in THP-1 and inhibits proliferation and colony formation of MV(4;11) (MLL-AF4) cells (EC50 <1nM). ORY-1001 d
价 格：￥电议型 号：T28269产 地：中国大陆
