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T72182Combretastatin A1 phosphate；化合物 Combretastatin A1 phosphateOxi4503|||CA1P|||Oxi4503 ; CA1P ; Combr
Combretastatin A1 phosphate, a potent vascular disruptive agent, exhibits anti-angiogenic effects on tumors and holds potential for research on pancreatic neuroendocrine tumors.
价 格：￥电议型 号：T72182产 地：中国大陆
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T72091ADRA1D receptor antagonist 1 free base；化合物 ADRA1D receptor antagonist 1 free baseADRA1D receptor ant
ADRA1D receptor antagonist 1 (free base) antagonist ( K i =1.6 nM). ADRA1D receptor antagonist 1 (free base) dose-dependently inhibits bladder contraction with an IC 30 value of 15 nM. ADRA1D receptor antagonist 1 (free base) can be used in studies of overactive bladder disorders such as urinary urgency, frequency and incontinence.
价 格：￥电议型 号：T72091产 地：中国大陆
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T71750Quinolactacin A1；化合物 (+)-Quinolactacin A1Quinolactacin A1
Quinolactacin A1, a powerful acetylcholinesterase (AChE) inhibitor, originates from the solid-state fermentation of Penicillium citrinum 90648. It is utilized in Alzheimer´s disease research.
价 格：￥电议型 号：T71750产 地：中国大陆
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T71317WS1358A1 disodium；化合物 WS1358A1 disodiumWS1358A1 disodium
WS1358A1 disodium is a potent inhibitor of renal dehydropeptidase.
价 格：￥电议型 号：T71317产 地：中国大陆
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T7131Antineoplaston A10；3-苯基乙酰氨基-2,6-哌啶二酮NSC-648539；3-苯基乙酰氨基-2,6-哌啶二酮|||NSC-648539
Antineoplaston A10 (NSC-648539) is a Ras inhibitor potentially for the treatment of glioma, lymphoma, astrocytoma and breast cancer.
价 格：￥电议型 号：T7131产 地：中国大陆
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T7098BAPTA化合物BAPTA1,2-双(2-氨基苯氧基)-乙烷-N,N,N`,N`-四乙酸
BAPTA is a neuroprotective agent in cerebral ischemia, acting as an intercellular Ca2+ chelator.
价 格：￥电议型 号：T7098产 地：中国大陆
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T7090Jionoside A1焦地黄苯乙醇苷A1焦地黄苯乙醇甙A1|||焦地黄苯乙醇苷A1
Jionoside A1 is isolated and purified from the roots of Rehmannia glutinosa. It displays dose-dependent immune-enhancement activity and possesses moderate neuroprotective activities on H2O2-treated SH-SY5Y cells.
价 格：￥电议型 号：T7090产 地：中国大陆
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T70692ST7612AA1；化合物ST7612AA1ST7612AA1
ST7612AA1 is a novel potent and oral HDCA inhibitor that acts as an HIV-1 latency reactivator. ST7612AA1 showed significant antitumor activity at low concentrations in vitro and in vivo. ST7612AA1 has potential anticancer activity and can be used to study malaria.
价 格：￥电议型 号：T70692产 地：中国大陆
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T70130NPA101.3；化合物 NPA101.3NPA101.3
NPA101.3 is a a Second-Generation RET/VEGFR2 Inhibitor. It is a potential clinical candidate for RET-driven cancers.
价 格：￥电议型 号：T70130产 地：中国大陆
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T69276KFA1982；化合物 KFA1982KFA1982
KFA1982 is a novel and potent factor Xa inhibitor.
价 格：￥电议型 号：T69276产 地：中国大陆
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T6868KYA1797K；化合物KYA1797KKYA1797K
KYA1797K is a highly potent and selective inhibitor. Wnt/β-catenin IC50 is 0.75 μM through TOPflash assay.
价 格：￥电议型 号：T6868产 地：中国大陆
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T6855HA15；化合物HA15HA15
HA15 targets specifically BiP/GRP78/HSPA5. HA15 exhibits anti-cancerous activity on all melanoma cells tested, including cells isolated from patients and cells that developed resistance to BRAF inhibitors.
价 格：￥电议型 号：T6855产 地：中国大陆
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T67916CYP4A11/CYP4F2-IN-2；化合物CYP4A11/CYP4F2-IN-2CYP4A11/CYP4F2-IN-2
CYP4A11/CYP4F2-IN-2 is a potent and orally active dual inhibitor of cytochrome P450 (CYP) 4A11 and CYP4F2, with IC50 values of 140 nM and 40 nM, respectively. CYP4A11/CYP4F2-IN-2 can be extracted from liver and kidney and has the potential to treat kidney diseases.
价 格：￥电议型 号：T67916产 地：中国大陆
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T67901SRD5A1-IN-1；化合物SRD5A1-IN-1SRD5A1-IN-1
SRD5A1-IN-1 is an inhibitor of steroid 5α-reductase type 1 (SRD5A1, IC50 = 1.44 ?M). SRD5A1-IN-1 lowers the production of dihydrotestosterone and shows a significant decrease in the SRD5A1 protein expression.
价 格：￥电议型 号：T67901产 地：中国大陆
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T67783trans-isrib A17；化合物ISR-IN-1ISR-IN-1；ISR-IN-1
trans-isrib A17 (ISR-IN-1) is an potent inhibitor of the integrated stress response with EC50 of 0.6 nM.
价 格：￥电议型 号：T67783产 地：中国大陆
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T67756ISRIB-A15；化合物ISR-IN-2ISR-IN-2；ISR-IN-2
ISRIB-A15 (ISR-IN-2) is an potent inhibitor of the integrated stress response with an EC50 of 0.8 nM.
价 格：￥电议型 号：T67756产 地：中国大陆
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T6749A-1331852；化合物A1331852A-1331852
A-1331852 is a potent and selectiveBCL-XL inhibitor and may be useful in the treatment of cancer, immune and autoimmune diseases.
价 格：￥电议型 号：T6749产 地：中国大陆
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T6748A-1155463；醋酸艾塞那肽A 1155463|||A1155463；A 1155463|||A1155463|||醋酸艾塞那肽
A-1155463, a highly potent and selective BCL-XL inhibitor, shows picomolar binding affinity to BCL-XL, and >1000-fold weaker binding to BCL-2 and related proteins BCL-W(Ki=19 nM) and MCL-1(Ki>440 nM).
价 格：￥电议型 号：T6748产 地：中国大陆
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T6740Bafilomycin A1巴佛洛霉素A1巴佛洛霉素A1|||巴佛洛霉素 A1
Bafilomycin A1 belongs to the macrolide class of antibiotics and is a V-ATPase (IC50=0.44 nM) that is specific and reversible. Bafilomycin A1 is an inhibitor of the late phase of autophagy, blocking the fusion of autophagosomes with lysosomes. Bafilomycin A1 also induces apoptosis.
价 格：￥电议型 号：T6740产 地：中国大陆
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T67250SingaCycle(TM)-A1；化合物 Chloro[[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](N,N-dimethylbenzylam
SingaCycle(TM)-A1 is a useful organic compound for research related to life sciences and the catalog number is T67250.
价 格：￥电议型 号：T67250产 地：中国大陆
