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T17222VelneperitS2367；韦利贝特
Velneperit is potent and selective neuropeptide Y (NPY) Y5 receptor under evaluating for treatment of obesity.
价 格：￥电议型 号：T17222产 地：中国大陆
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T17225-Amino-4-imidazolecarboxamide
5-Amino-4-imidazolecarboxamide is an imidazole derivative.
价 格：￥电议型 号：T1722产 地：中国大陆
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T17219Vatalanib free base
Vatalanib is a VEGFR2/KDR inhibitor (IC50: 37 nM).
价 格：￥电议型 号：T17219产 地：中国大陆
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T17218Varespladib methylLY333013；A-002
Varespladib methyl, a bioavailable prodrug of Varespladib, is a selective group II secretory phospholipase A2 inhibitor.
价 格：￥电议型 号：T17218产 地：中国大陆
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T17217VamoroloneVBP15；地塞米松EP杂质E
Vamorolone is an orally active dissociative steroidal anti-inflammatory drug and membrane-stabilizer. Vamorolone improves muscular dystrophy without side effects. Vamorolone displays effective NF-κB inhibition and substantially decreases hormonal effects.
价 格：￥电议型 号：T17217产 地：中国大陆
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T17212VAL-0831,2:5,6-二脱水半乳糖醇；去水卫矛醇；Dianhydrodulcitol；Dianhydrogalactitol
VAL-083 is an alkylating compound that creates N7 methylation on DNA. It also has antitumor activity.
价 格：￥电议型 号：T17212产 地：中国大陆
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T17209UVI 3003
UVI 3003 is a highly selective antagonist of the retinoid X receptor. UVI 3003 inhibits Xenopus and human RXRα in Cos7 cells (IC50s: 0.22 and 0.24 μM, respectively).
价 格：￥电议型 号：T17209产 地：中国大陆
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T17208USL311
USL311 is a CXCR4 receptor antagonist which prevents the binding of stromal-cell derived factor-1 (SDF-1 or CXCL12) to CXCR4. USL311 inhibits CXCR4 activation and decreases proliferation and migration of CXCR4-expressing tumor cells, with anti-tumor activ
价 格：￥电议型 号：T17208产 地：中国大陆
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T17205UNC2541
UNC2541 is a potent and Mer tyrosine kinase (MerTK)-specific inhibitor. It also binds in the MerTK ATP pocket (IC50: 4.4 nM). UNC2541 inhibits phosphorylated MerTK (pMerTK; EC50, 510 nM).
价 格：￥电议型 号：T17205产 地：中国大陆
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T17204UNC0321
UNC0321 is inactive against SET7/9, SET8/PreSET7, PRMT3, and JMJD2E. UNC0321 is an effective and selective histone methyltransferase G9a inhibitor (Ki: 63 pM) and (assay-dependent IC50: 6-9 nM). UNC0321 also inhibits GLP (assay-dependent IC50: 15-23 nM).
价 格：￥电议型 号：T17204产 地：中国大陆
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T17203UNC0224
UNC0224 is inactive against SET7/9, SET8/PreSET7, PRMT3, and JMJD2E. UNC0224 is a potent and selective histone methyltransferase G9a inhibitor (Ki: 2.6 nM, an IC50 of 15 nM, and a Kd of 23 nM). UNC0224 also potently inhibits b>GLP (assay-dependent IC50: 2
价 格：￥电议型 号：T17203产 地：中国大陆
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T1720Amfenac Sodium Hydrate一水氨芬酸钠；氨芬酸钠水合物；Amfenac Sodium Monohydrate
Amfenac Sodium monohydrate is a non-steroidal analgesic anti-inflammatory drug with acetic acid moiety.
价 格：￥电议型 号：T1720产 地：中国大陆
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T17196UC-1728t-TUCB
UC-1728 is an effective rabbit soluble epoxide hydrolase inhibitor (IC50: 2 nM on rabbit liver).
价 格：￥电议型 号：T17196产 地：中国大陆
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T17172Trofosfamide
Trofosfamide is a derivative of oxazaphosphorine with antineoplastic potency.
价 格：￥电议型 号：T17172产 地：中国大陆
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T16888SJ-172550
SJ-172550 is a small molecule inhibitor of MDMX (EC50: 5 μM).
价 格：￥电议型 号：T16888产 地：中国大陆
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T15244Ertugliflozin L-pyroglutamic acidPF-04971729 L-pyroglutamic acid
Ertugliflozin L-pyroglutamic acid is a selective and orally active hSGLT2 inhibitor with an IC50 of 0.877 nM. Ertugliflozin L-pyroglutamic acid can be used for studies about the treatment of type 2 diabetes mellitus.
价 格：￥电议型 号：T15244产 地：中国大陆
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T14765BOS-172722
BOS-172722 is an inhibitor of monopolar spindle 1 (MPS1) checkpoint(IC50 of 2 nM).
价 格：￥电议型 号：T14765产 地：中国大陆
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T11728JR-AB2-011
JR-AB2-011 inhibits mTORC2 activity by blocking Rictor-mTOR association (Ki: 0.19 μM). JR-AB2-011 has anti-glioblastoma multiforme (GBM) properties. JR-AB2-011 is a selective mTORC2 inhibitor with an IC50 value of 0.36 μM.
价 格：￥电议型 号：T11728产 地：中国大陆
