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T15668KT185KT185
KT185 is an orally-bioavailable and brain-penetrant ABHD6 inhibitor (IC50: 0.21 nM in Neuro2A cells).
价 格：￥电议型 号：T15668产 地：美洲
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T1850BalicatibBalicatib,AAE581,
Balicatib is a potent and selective inhibitor of cathepsin K, used in trials studying the treatment of osteoporosis.
价 格：￥电议型 号：T1850产 地：美洲
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T1851ZM 336372ZM 336372,Zinc00581684,
ZM 336372 is a potent and selective c-Raf inhibitor.
价 格：￥电议型 号：T1851产 地：美洲
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T1852BelinostatBelinostat,NSC726630,PX-105684
Belinostat is a novel hydroxamic acid-type histone deacetylase (HDAC) inhibitor with antineoplastic activity. Belinostat targets HDAC enzymes, thereby inhibiting tumor cell proliferation, inducing apoptosis, promoting cellular differentiation, and inhibit
价 格：￥电议型 号：T1852产 地：美洲
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T1853NMS 873NMS 873
NMS-873 is a potent, selective allosteric VCP/p97 inhibitor.
价 格：￥电议型 号：T1853产 地：美洲
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T1854MS436MS436
MS436 is a selective, small-molecule inhibitor for the BRD4 bromodomains.
价 格：￥电议型 号：T1854产 地：美洲
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T1856TPT-260TPT-260,TPT260,TPT 260
TPT-260 is a thiophene thiourea derivative with molecule weight 260.00 in free base form.
价 格：￥电议型 号：T1856产 地：美洲
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T1857TMP269TMP269
TMP269 is an effective, specific class IIa HDAC inhibitor for HDAC4 (IC50: 157 nM), HDAC5 (IC50: 97 nM), HDAC7 (IC50: 43 nM), and HDAC9 (IC50: 23 nM), respectively.
价 格：￥电议型 号：T1857产 地：美洲
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T1859AZD8055AZD8055
AZD8055 is an ATP-competitive mTOR inhibitor (IC50: 0.8 nM in MDA-MB-468 cells). It is ~1,000-fold selective for mTOR over all PI3K isoforms.
价 格：￥电议型 号：T1859产 地：美洲
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T2185Sodium L-ascorbyl-2-phosphateSodium L-ascorbyl-2-phosphate,2-Phospho-L-ascorbic acid trisodium salt,
L-Ascorbic acid 2-phosphate (AA2P) is used in biocatalytic dephosphorylation for electric power generation and electrochemical detection assays.
价 格：￥电议型 号：T2185产 地：美洲
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T2382VemurafenibVemurafenib,PLX4032,RO5185426
Vemurafenib (PLX4032) is a novel and potent B-Raf (V600E) inhibitor (IC50: 31 nM).
价 格：￥电议型 号：T2382产 地：美洲
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T2530LevosimendanLevosimendan,OR1259,OR1855
Levosimendan is a calcium sensitizer used in the management of acutely decompensated congestive heart failure. It increases the sensitivity of the heart to calcium, thus increasing cardiac contractility without a rise in intracellular calcium. Levosimenda
价 格：￥电议型 号：T2530产 地：美洲
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T5185PZ-2891PZ-2891
PZ-2891 is an orally bioavailable, brain penetrant pantothenate kinase (PANK) modulator(hPANK3,IC50:1.3 nM).
价 格：￥电议型 号：T5185产 地：美洲
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T5211NSC185058NSC185058
NSC 185058 is an inhibitor of ATG4B, a major cysteine protease. It also can attenuate the autophagic activity.
价 格：￥电议型 号：T5211产 地：美洲
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T6185Gambogic AcidGambogic Acid,Beta-Guttiferrin,Guttatic Acid
Gambogic Acid ( EC50=0.78-1.64 uM) activates caspases. Gambogic Acid competitively suppresses Bcl-XL, Bcl-2, Bcl-W, Bcl-B, Bfl-1 and Mcl-1. The IC50s of Gambogic Acid for Bcl-XL, Bcl-2, Bcl-W, Bcl-B, Bfl-1 and Mcl-1 are 1.47, 1.21, 2.02, 0.66, 1.06 and 0
价 格：￥电议型 号：T6185产 地：美洲
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T83498[D-Phe2,D-Ala6]-LH-RH；化合物 [D-Phe2,D-Ala6]-LH-RHWy 18185；Wy 18185
[D-Phe2,D-Ala6]-LH-RH is a potent luteinizing hormone-releasing hormone (LH-RH) antagonist with demonstrated activities against LH/FSH-RH and an ability to inhibit ovulation [1].
价 格：￥电议型 号：T83498产 地：中国大陆
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T83185AChE-IN-43；化合物 AChE-IN-43AChE-IN-43
AChE-IN-43 is a potent, selective AChE inhibitor with a K i of 0.41 μM, applicable in the study of neurological diseases [1].
价 格：￥电议型 号：T83185产 地：中国大陆
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T82185Hortein；化合物 HorteinHortein
Hortein, a natural product derived from the fungus Hortaea werneckii, is associated with the sponge Aplysina aerophoba [1].
价 格：￥电议型 号：T82185产 地：中国大陆
