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T12153N-type calcium channel blocker-1；化合物 T12153N-type calcium channel blocker-1
N-type calcium channel blocker-1 is an orally active analgesic agent,shows high affinity to functionally block N-type calcium channels.
价 格：￥电议型 号：T12153产 地：中国大陆
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T11609ICI 153110；化合物 T11609ICI 153110
ICI 153110 is an orally active phosphodiesterase inhibitor with both inotropic and vasodilating properties. It is designed for the treatment of congestive cardiac failure.
价 格：￥电议型 号：T11609产 地：中国大陆
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T11539HCV-IN-29；达卡他韦中间体HCV-IN-29
HCV-IN-29 is a hepatitis C virus (HCV) inhibitor.
价 格：￥电议型 号：T11539产 地：中国大陆
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T11538Hck-IN-1；化合物Hck-IN-1Hck-IN-1
Hck-IN-1 is a selective Nef-dependent Hck inhibitor (IC50s: 2.8 μM and >20 μM for Nef:Hck complex and Hck) with antiretroviral activity. Hck-IN-1 is a direct and wide HIV-1 Nef antagonist with an IC50 of 100-300 nM for wild-type HIV-1 replication.
价 格：￥电议型 号：T11538产 地：中国大陆
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T11537HAT-IN-1；化合物 T11537HAT-IN-1
HAT-IN-1 is an inhibitor of HAT used in the research of cancer.
价 格：￥电议型 号：T11537产 地：中国大陆
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T11535Haloperidol D4氟哌啶醇D4氟哌啶醇D4
Haloperidol D4 is deuterium-labeled haloperidol.
价 格：￥电议型 号：T11535产 地：中国大陆
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T11534LHaemanthamine hydrochloride (466-75-1 free base)；化合物 T11534LHaemanthamine hydrochloride；Haemanthamin
Haemanthamine hydrochloride is an alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. It inhibits protein biosynthesis during the elongation stage of translation. It has antimalarial, pro-apoptotic, antiviral, antioxidant, and anticonvulsant activities.
价 格：￥电议型 号：T11534L产 地：中国大陆
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T11534Haemanthamine；化合物 T11534Haemanthamine
Haemanthamine is an alkaloid isolated from the Amaryllidaceae plants with potent anticancer activity. It inhibits protein biosynthesis during the elongation stage of translation. It has antimalarial, pro-apoptotic, antiviral, antioxidant, and anticonvulsant activities.
价 格：￥电议型 号：T11534产 地：中国大陆
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T11533Z-HA155；化合物Z-HA155CS-963；CS-963
Z-HA155 (CS-963) selectively and potently inhibits autotaxin with an IC50 of 5.7 nM.
价 格：￥电议型 号：T11533产 地：中国大陆
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T11532H4R antagonist 1；化合物 T11532H4R antagonist 1
H4R antagonist 1 is a highly selective histamine H4 receptor (H4R) antagonist (IC50: 27 nM). H4R antagonist 1 does not show any noticeable binding affinity to other subtypes of histamine receptors, H1R, H2R, and H3R.
价 格：￥电议型 号：T11532产 地：中国大陆
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T11531H3R-IN-1 Hydrochloride化合物 T11531H-3R-IN-1 Hydrochloride|||H3R IN 1 Hydrochloride|||H3RIN1 Hydrochlor
H3R-IN-1 Hydrochloride is an inverse agonist of histamine receptor 3( H3R ) .
价 格：￥电议型 号：T11531产 地：中国大陆
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T11530LH3B-6545；化合物 T11530LH3B-6545
H3B-6545 is an oral and selective antagonist of estrogen receptor covalent (SERCA).
价 格：￥电议型 号：T11530L产 地：中国大陆
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T11530H3B-6545 Hydrochloride；化合物 T11530H3B-6545 Hydrochloride
H3B-6545 Hydrochloride is a selective, oral estrogen receptor covalent antagonist (SERCA).
价 格：￥电议型 号：T11530产 地：中国大陆
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T1153Trimethoprim；甲氧苄啶NIH 204|||BW 56-72|||NSC-106568；NIH 204|||BW 56-72|||甲氧苄啶|||NSC-106568
Trimethoprim (NSC-106568) is a Dihydrofolate Reductase Inhibitor Antibacterial. The mechanism of action of trimethoprim is as a Dihydrofolate Reductase Inhibitor, and Cytochrome P450 2C8 Inhibitor, and Organic Cation Transporter 2 Inhibitor.
价 格：￥电议型 号：T1153产 地：中国大陆
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T11153EG00229；化合物 T11153EG00229
EG00229 is a neuropilin 1 (NRP1) receptor antagonist that selectively inhibits the binding of VEGF-A to the NRP1 b1 domain, achieving this inhibition with an IC50 value of 3 μM. It does not affect the binding of VEGF-A to other receptors, such as VEGFR-1 and VEGFR-2.
价 格：￥电议型 号：T11153产 地：中国大陆
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T10939LL-Cystathionine；L-胱硫醚Cystathionine|||ZINC1532680|||L-(+)-Cystathionine|||Cystathionine, L-；L-胱硫醚|||C
L-Cystathionine (Cystathionine, L-) is a key nonprotein amino acid related to metabolic conditions of sulfur-containing amino acids. L-Cystathionine can be used in studies about cardiovascular protection.
价 格：￥电议型 号：T10939L产 地：中国大陆
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T10865LCot inhibitor-1 hydrochloride；化合物Cot inhibitor-1盐酸盐Cot inhibitor-1 hydrochloride(915365-57-0 Free ba
Cot inhibitor-1 hydrochloride is an inhibitor of tumor progression loci-2 kinase (IC50 = 28 nM) and inhibits the production of TNF-α in human whole blood (IC50 = 5.7 nM).
价 格：￥电议型 号：T10865L产 地：中国大陆
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T10780CGP-53153；化合物 T10780CGP-53153
CGP-53153 is a steroidal inhibitor of 5 alpha-reductase (IC50s: 36 and 262 nM in rat and human prostatic tissue).
价 格：￥电议型 号：T10780产 地：中国大陆
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T10718LCCT241533 hydrochloride；化合物 T10718LCCT241533 hydrochloride
CCT241533 hydrochloride is an effective and selective ATP competitive inhibitor of CHK2 (Ki: 1.16 nM; IC50: 3 nM).
价 格：￥电议型 号：T10718L产 地：中国大陆
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T10718CCT241533；化合物 T10718CCT241533
CCT241533 is an effective and selective ATP competitive inhibitor of CHK2 (Ki: 1.16 nM; IC50: 3 nM).
价 格：￥电议型 号：T10718产 地：中国大陆
