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T6975Sarcosineinhibit,dysfunction,schizophrenia,Endogenous Metabolite,Sarcosine,Inhibitor,cognitive,depre
Sarcosine is a competitive inhibitor of the type I glycine transporter (GlyT1) and an N-methyl-D-aspartate receptor (NMDAR) co-agonist.
价 格：￥电议型 号：T6975产 地：中国大陆
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T16975TAK-593
TAK-593 is an effective VEGFR and PDGFR family inhibitor (IC50s: 3.2, 0.95, 1.1, 4.3, and 13 nM for VEGFR1, VEGFR2, VEGFR3, PDFGRα, and PDFGRβ, respectively).
价 格：￥电议型 号：T16975产 地：中国大陆
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T1403ClimbazoleBAY-e 6975；甘宝素
Climbazole is a broad-spectrum imidazole antifungal agent with anti-dandruff benefits.
价 格：￥电议型 号：T1403产 地：中国大陆
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T1403ClimbazoleClimbazole,BAY-e 6975,
Climbazole is a broad-spectrum imidazole antifungal agent with anti-dandruff benefits.
价 格：￥电议型 号：T1403产 地：美洲
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T76975Tomaralimab；托拉利单抗OPN-305；OPN-305
Tomaralimab (OPN-305) is a humanized IgG4 monoclonal antibody targeting TLR2. Tomarlimab is used to study myelodysplastic syndromes (MDS).
价 格：￥电议型 号：T76975产 地：中国大陆
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T69759IACS-9439；化合物 IACS-9439IACS-9439
IACS-9439 is a potent, selective, and orally active inhibitor of CSF1R, exhibiting a K(i) of 1 nM. It is applicable in the research of advanced solid tumors [1].
价 格：￥电议型 号：T69759产 地：中国大陆
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T69758Flutamide-d7；化合物 Flutamide-d7Flutamide-d7
Flutamide-d7 is intended for use as an internal standard for the quantification of flutamide by GC- or LC-MS. Flutamide is an androgen receptor antagonist and prodrug form of 2-hydroxy flutamide. Flutamide is converted to 2-hydroxy flutamide by the cytochrome P450 (CYP) isoform CYP1A2 in human liver microsomes. It is cytotoxic to PC3 and LNCaP prostate cancer cells with IC50 values of 98.8 and 81.8 ?M, respectively. Flutamide (50 mg/kg per day) reduces tumor growth in a PC-82 mouse xenograft mo
价 格：￥电议型 号：T69758产 地：中国大陆
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T69757PDDC inhibitor；PDDC 抑制剂PDDC inhibitor
PDDC inhibitor (Phenyl (R)-(1-(3-(3,4-dimethoxyphenyl)-2,6-dimethylimidazo[1,2-b]pyridazin-8-yl)pyrrolidin-3-yl)carbamate) is a selective and highly potent nSMase2 inhibitor.
价 格：￥电议型 号：T69757产 地：中国大陆
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T69756GT-2331；化合物 GT-2331GT-2331
GT-2331 is a histamine H3 receptor antagonist.
价 格：￥电议型 号：T69756产 地：中国大陆
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T69755Evatanepag sodium；化合物 Evatanepag sodiumEvatanepag sodium
Evatanepag, also known as CP-533536, is an EP2 receptor selective prostaglandin E2 (PGE2) agonist that induces local bone formation. CP-533536 demonstrated the ability to heal fractures when administered locally as a single dose in rat models of fracture healing.
价 格：￥电议型 号：T69755产 地：中国大陆
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T69754BTP1；化合物 BTP1BTP1
BTP1 is an inhibitor of NFAT activation and T-cell cytokine production. BTP1 potently inhibits SOCE in many cells with considerable selectivity over voltage-gated Ca2+ entry.
价 格：￥电议型 号：T69754产 地：中国大陆
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T69753HDAC6 degrader 9c；HDAC6 降解剂9cHDAC6 degrader 9c
HDAC6 degrader 9c is a small molecule histone deacetylase 6 (HDAC6) degrader that can be used to study cancer or other diseases.
价 格：￥电议型 号：T69753产 地：中国大陆
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T69752BRD1991；化合物 BRD1991BRD1991
BRD1991 is a chemical compound that specifically disrupts the interaction between Beclin 1 and Bcl-2, thereby inducing autophagy. It accomplishes this without initiating apoptosis or other forms of cell death.
价 格：￥电议型 号：T69752产 地：中国大陆
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T69751UK-356202；化合物 UK-356202UK-356202
UK-356,202 is a potent and selective urokinase-type plasminogen activator (Ki = 37 nM). Urokinase plasminogen activator (uPA, urokinase) is a trypsinlike serine protease and a therapeutical target for many cancer types, including breast, ovarian, and pancreatic cancer. uPA is a valuable oncology target.
价 格：￥电议型 号：T69751产 地：中国大陆
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T69750p-MPPF dihydrochloride；化合物 p-MPPF dihydrochloridep-MPPF dihydrochloride
p-MPPF dihydrochloride is a selective 5-ht1a serotonin receptor antagonist
价 格：￥电议型 号：T69750产 地：中国大陆
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T6975Sarcosine肌氨酸Sarcosinic acid|||Methylaminoacetic acid|||Sarcosin|||肌氨酸|||Methylglycine|||N-Methylamin
Sarcosine (Methylglycine) is a competitive inhibitor of the type I glycine transporter (GlyT1) and an N-methyl-D-aspartate receptor (NMDAR) co-agonist.
价 格：￥电议型 号：T6975产 地：中国大陆
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T66975tert-Butyl ((2S,3R)-4-chloro-3-hydroxy-1-phenylbutan-2-yl)carbamate；化合物 tert-Butyl ((2S,3R)-4-chloro
tert-Butyl ((2S,3R)-4-chloro-3-hydroxy-1-phenylbutan-2-yl)carbamate is a useful organic compound for research related to life sciences. The catalog number is T66975 and the CAS number is 162536-40-5.
价 格：￥电议型 号：T66975产 地：中国大陆
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T64362AZD0780；化合物AZD0780PCSK9-IN-12|||EX-A6975；PCSK9-IN-12|||EX-A6975
AZD0780 (EX-A6975) exhibits bind affinity for PCSK9 ( Kd ＜200 nM). AZD0780 has research value in cholesterol metabolism.
价 格：￥电议型 号：T64362产 地：中国大陆
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T36975EZM0414 TFA；EZM0414 三氟乙酸盐IPN-60210 TFA|||SETD2-IN-1 TFA；IPN-60210 TFA|||SETD2-IN-1 TFA
EZM0414 TFA (SETD2-IN-1 TFA) is a SETD2 inhibitor with anticancer and antiproliferative effects for the study of leukemia and immune dysfunction.
价 格：￥电议型 号：T36975产 地：中国大陆
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T34404RP-69758；化合物 T34404RP69758|||RP-69758|||RP 69758|||RP69758|||RP 69758|||RP69758|||RP 69758；RP69758||
RP-69758 is a bioactive chemical.
价 格：￥电议型 号：T34404产 地：中国大陆
