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T27224DX-9065A HCl hydrate；化合物 T27224DX9065|||DX 9065|||DX9065A|||DX 9065A|||DX-9065A|||DX-9065；DX9065|||D
DX-9065A is a factor Xa inhibitor. DX-9065a inhibits proinflammatory events induced by factor Xa and gingipains. DX-9065a is a competitive inhibitor of the Spectrozyme FXa (SpFXa) cleavage by both fXa and prothrombinase with similar K(i) values of approximately 10-20 nM.
价 格：￥电议型 号：T27224产 地：中国大陆
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T26945Capoamycin；化合物 T26945AC-54|||AC54|||AC 54；AC-54|||AC54|||AC 54
Capoamycin is an insotatracine antibiotic investigated for anti tumor properties.
价 格：￥电议型 号：T26945产 地：中国大陆
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T26915BTG-1640；化合物 T26915ABIO-0801|||ABIO-08-01|||SP-1640；ABIO-0801|||ABIO-08-01|||SP-1640
BTG-1640 is used potentially for the treatment of anxiety and panic disorder.
价 格：￥电议型 号：T26915产 地：中国大陆
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T26725AZD-9684；化合物 T26725AZD9684|||AZD 9684；AZD9684|||AZD 9684
AZD-9684, a carboxypeptidase U inhibitor, is used potentially for the prevention of thrombosis.
价 格：￥电议型 号：T26725产 地：中国大陆
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T26715AZD-3289；化合物 T26715AZD 3289；AZD 3289
AZD-3289, a potent BACE1 inhibitor, is used potentially for the treatment of Alzheimer´s disease.
价 格：￥电议型 号：T26715产 地：中国大陆
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T26705AZ-4217；化合物 T26705AZ4217|||AZ 4217；AZ4217|||AZ 4217
AZ-4217 is a high potency BACE inhibitor. It displays acute central efficacy in different in vivo models and reduced amyloid deposition in Tg2576 mice. AZ-4217 has IC50 160 pM in human SH-SY5Y cells with an excellent in vivo efficacy.
价 格：￥电议型 号：T26705产 地：中国大陆
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T26695AX15839；化合物 T26695AX-15839|||AX 15839；AX-15839|||AX 15839
AX15839 is an inhibitor of BRD4 and ERK5.
价 格：￥电议型 号：T26695产 地：中国大陆
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T26675AT-9283 HCl；化合物 T26675AT-9283|||AT-9283 hydrochloride|||AT9283|||AT 9283；AT-9283|||AT-9283 hydrochlo
AT-9283, a multi-targeted kinase inhibitor, is used potentially for the treatment of multiple myeloma.
价 格：￥电议型 号：T26675产 地：中国大陆
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T26665AS604872；化合物 T26665AS-604872|||AS 604872；AS-604872|||AS 604872
AS604872 is a selective antagonist of the FP receptor.. AS604872 significantly accelerated degeneration of the media in both cerebral artery and aorta as evidenced by thinning of the media and disruption of the elastic lamina and promoted IA and aortic dissection. AS604872 can be used to make models of these vascular diseases with extensive degeneration. AS604872 also inhibits spontaneous uterine contraction
价 格：￥电议型 号：T26665产 地：中国大陆
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T26635Antifolate C1；化合物 T26635AGF 94|||AGF94|||AGF-94；AGF 94|||AGF94|||AGF-94
Antifolate C1 is an inhibitor of de novo purine biosynthesis. Antifolate C1 has selectivity for cellular uptake by high affinity folate receptors and the proton-coupled folate transporter (PCFT) over the reduced folate carrier (RFC).
价 格：￥电议型 号：T26635产 地：中国大陆
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T26615Amdoxovir；化合物 T26615AMDX|||DAPD；AMDX|||DAPD
Amdoxovir is a reverse transcriptase inhibitor.
价 格：￥电议型 号：T26615产 地：中国大陆
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T26605Alyssin；化合物 T26605Alyssin
Alyssin is a sulforaphane homolog and antioxidant. It induces phase II enzymes and increases Nrf2 levels in adenocarcinoma cells. It decreases the metabolism of polycyclic aromatic hydrocarbons, supressing the risk of carcinogenesis in vitro.
价 格：￥电议型 号：T26605产 地：中国大陆
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T26595Allosamidin；化合物 T26595A-82516|||A 82516|||A82516；A-82516|||A 82516|||A82516
Allosamidin, a chitinase inhibitor and typical secondary metabolite of Streptomyces, may be used as a pesticide and anti-asthmatic agent.
价 格：￥电议型 号：T26595产 地：中国大陆
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T26575AGI-026；化合物 T26575AGI026；AGI026
AGI-026 is a potent, selective inhibitor of the human IDH2R140Q-mutant enzyme.
价 格：￥电议型 号：T26575产 地：中国大陆
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T26535AC 915；化合物 T26535AC915|||AC-915；AC915|||AC-915
AC 915 is a sigma-1 antagonist.
价 格：￥电议型 号：T26535产 地：中国大陆
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T26525ABT-281；化合物 T26525ABT 281|||A-86281|||A 86281|||ABT281|||A86281；ABT 281|||A-86281|||A 86281|||ABT281
ABT-281 is an ascomycin analog and a macrolactam T cell inhibitors with potent topical activity and reduced systemic exposure.
价 格：￥电议型 号：T26525产 地：中国大陆
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T26505AB023b；化合物 T26505AB-023b|||AB 023b；AB-023b|||AB 023b
AB023b is an antibiotic with antifungal properties.
价 格：￥电议型 号：T26505产 地：中国大陆
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T26495AA560；化合物 T26495AA 560|||AA-560；AA 560|||AA-560
AA560 is a nonsteroidal antiandrogen. AA560 decreases the uptake of 3H-androgens in the ventral prostate and decreases the weight of accessory organs.
价 格：￥电议型 号：T26495产 地：中国大陆
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T26485A778317；化合物 T26485A778317
A778317 is a stereoselective, high-affinity antagonist.
价 格：￥电议型 号：T26485产 地：中国大陆
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T26475A-286501；化合物 T26475A-286501
A-286501 is an orally active adenosine kinase inhibitor (IC50=0.47 nM). A-286501 effectively attenuates nociception by a non-opioid, non-non-steroidal anti-inflammatory drug ADO, receptor mediated mechanism.
价 格：￥电议型 号：T26475产 地：中国大陆
