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T10929LD-3263 hydrochloride；化合物D-3263 盐酸盐EC D-3263 HCl|||D3263 HCl salt；EC D-3263 HCl|||D3263 HCl salt
D-3263 hydrochloride (D3263 HCl salt) is enteric-coated, orally bioavailable transient receptor potential melatonin member 8 (TRPM8) agonist.
价 格：￥电议型 号：T10929L产 地：中国大陆
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T10929D-3263；化合物 T10929D-3263
D-3263 is an agonist of transient receptor potential melatonin member 8 (TRPM8) with potential antitumor activity.
价 格：￥电议型 号：T10929产 地：中国大陆
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T1084Apramycin sulfate；硫酸安普霉素Nebramycin II|||Ai3-29795；Nebramycin II|||Ai3-29795|||硫酸安普霉素|||硫酸阿布拉霉素
Apramycin sulfate (Nebramycin II) is an aminoglycoside antibiotic.
价 格：￥电议型 号：T1084产 地：中国大陆
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T10835L1Cletoquine hydrochloride；盐酸氯托喹Cletoquine hydrochloride( 4298-15-1 Free base)；Cletoquine hydrochlorid
Cletoquine hydrochloride is a major active metabolite of Hydroxychloroquine. Cletoquine hydrochloride is a Chloroquine derivative and exhibits the ability to against the chikungunya virus (CHIKV). Cletoquine hydrochloride exhibits antimalarial effects.
价 格：￥电议型 号：T10835L1产 地：中国大陆
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T10829CKI-7 free base；化合物 T10829CKI-7；CKI-7
CKI-7 free base is a potent and ATP-competitive inhibitor of casein kinase 1 (CK1; IC50: 6 μM; Ki: 8.5 μM) and a selective Cdc7 kinase inhibitor. CKI-7 free base also inhibits SGK, ribosomal S6 kinase-1 (S6K1), and MSK1.
价 格：￥电议型 号：T10829产 地：中国大陆
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T10759CEP-28122 mesylate salt (1022958-60-6 free base)；化合物CEP-28122 mesylate saltCEP-28122 mesylate salt；C
CEP-28122 mesylate salt (1022958-60-6 free base) is a highly selective orally active ALK inhibitor (IC50: 1.9 nM in an enzyme-based TRF assay).
价 格：￥电议型 号：T10759产 地：中国大陆
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T10712CCR2 antagonist 3；化合物CCR2 antagonist 3AZD-2927|||AZD2927；AZD-2927|||AZD2927
CCR2 antagonist 3 (AZD-2927) is an antagonist of CCR2.
价 格：￥电议型 号：T10712产 地：中国大陆
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T10629Btk inhibitor 2；化合物Btk inhibitor 2BGB-3111 analog；BGB-3111 analog
Btk inhibitor 2 (BGB-3111 analog) is a BTK inhibitor.
价 格：￥电议型 号：T10629产 地：中国大陆
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T10603BRD-6929；化合物BRD-6929BRD-6929
BRD-6929 is a selective, brain-penetrant HDAC1 and HDAC2 inhibitor (IC50: ?1 and 8 nM). BRD-6929 (Cpd-60) shows high-affinity to HDAC1 and HDAC2 (Kis: 0.2 and 1.5 nM) [2]. BRD-6929 potentiates the efficacy of gnidimacrin (a PKC Agonist) against latent HIV-1. BRD-6929 can be used for mood-related behavioral model research[3].
价 格：￥电议型 号：T10603产 地：中国大陆
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T10529BF-168化合物 T10529BF168|||BF 168
BF-168 is a candidate probe for PET and specifically recognizes both neuritic and diffuse plaques (Ki: 6.4 nM for Aβ1-42).
价 格：￥电议型 号：T10529产 地：中国大陆
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T1050Prazosin hydrochloride哌唑嗪盐酸盐Prazosin hydrochloride|||哌唑嗪盐酸盐|||Prazosin HCl|||cp-12299-1|||Peripress|
Prazosin hydrochloride (Vasoflex) reduces peripheral resistance and relaxes vascular smooth muscles as a selective adrenergic alpha-1 antagonist by a mechanism not completely known. Prazosin hydrochloride is a synthetic piperazine derivative with hypotensive antiadrenergic properties, It is used in the treatment of heart failure, hypertension, pheochromocytoma, Raynaud´s syndrome, prostatic hypertrophy, and urinary retention.
价 格：￥电议型 号：T1050产 地：中国大陆
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T10469BAY-298；化合物 T10469BAY-298
BAY-298 is an orally active and selective luteinizing hormone receptor (LH-R) antagonist with IC 50 s of 96 nM, 23 nM and 78 nM for hLH (human LH) and rLH (rat LH) and cLH (cynomolgus monkey LH), respectively. BAY-298 is the first nanomolar hLH-R antagonist reducing sex hormone levels in vivo[1].
价 格：￥电议型 号：T10469产 地：中国大陆
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T10433Osimertinib dimesylate奥希替尼二甲磺酸盐奥希替尼二甲磺酸盐|||Mereletinib (dimesylate)|||AZD-9291 (dimesylate)
Osimertinib dimesylate is an irreversible and mutant selective EGFR inhibitor (IC50s: 12 and 1 nM against EGFR L858R and EGFR L858R/T790M).
价 格：￥电议型 号：T10433产 地：中国大陆
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T10432LAZD-8529 mesylate；化合物AZD-8529 mesylateAZD-8529 mesylate
AZD-8529 mesylate is a highly selective, and orally bioavailable positive allosteric modulator of mGluR2 (EC50: 285 nM). It shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6, 7, and 8 subtypes.
价 格：￥电议型 号：T10432L产 地：中国大陆
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T10432AZD-8529；化合物 T10432AZD-8529
AZD-8529 is a highly selective, and orally bioavailable positive allosteric modulator of mGluR2 (EC50: 285 nM). It shows no positive allosteric modulator responses at 20-25 M on the mGluR1, 3, 4, 5, 6, 7, and 8 subtypes.
价 格：￥电议型 号：T10432产 地：中国大陆
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T10429Tizaterkib；化合物AZD-0364AZD-0364；AZD-0364
Tizaterkib (AZD-0364) is a potent and selective ERK2 inhibitor.
价 格：￥电议型 号：T10429产 地：中国大陆
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T10329anti-TB agent 1；化合物anti-TB agent 1anti-TB agent 1
anti-TB agent 1 is a potent and orally active anti-tuberculosis agent (MICs: < 2 nM against the Mtb strains H37Rv, rRMP and rINH).
价 格：￥电议型 号：T10329产 地：中国大陆
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T10319LAnamorelin Fumarate；富马酸阿拉莫林ONO-7643 Fumarate|||RC1291 Fumarate；ONO-7643 Fumarate|||RC1291 Fumarate||
Anamorelin Fumarate is a novel ghrelin receptor agonist (EC50: 0.74 nM in the FLIPR assay).
价 格：￥电议型 号：T10319L产 地：中国大陆
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T10299AMG PERK 44；化合物 AMG PERK 44AMG PERK 44
AMG PERK 44 is an orally active and selective PERK inhibitor (IC50: 6 nM) that induces autophagy.AMG PERK 44 inhibits GCN2 (IC50: 7300 nM) and B-Raf (IC50 >1000 nM) and can be used in the study of cancer.
价 格：￥电议型 号：T10299产 地：中国大陆
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T10298L2AMG-548 dihydrochloride (864249-60-5 free base)；化合物 T10298L2AMG-548 dihydrochloride；AMG-548 dihydroc
AMG-548 dihydrochloride is an orally active and selective p38α inhibitor (Ki: 0.5 nM) and shows slightly selective over p38β (Ki: 36 nM) and >1000 fold selective against p38γ/p38δ. It is also extremely potent in the inhibition of whole blood LPS stimulated TNFα (IC50: 3 nM).
价 格：￥电议型 号：T10298L2产 地：中国大陆
