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T40211eIF4E-IN-1eIF4E-IN-1eIF4E-IN-1
eIF4E-IN-1 (WO2021003194A1, compound Y), is a highly effective inhibitor of eIF4E, a key protein involved in immunosuppression. By targeting immune checkpoint proteins such as PD-1, PD-L1, LAG3, TIM3, and IDO, eIF4E-IN-1 functions to disrupt immune suppression and promote immune release in specific diseases such as cancer and infectious diseases.
价 格：￥电议型 号：T40211产 地：中国大陆
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T40210eIF4E-IN-3eIF4E-IN-3eIF4E-IN-3
eIF4E-IN-3 is a highly effective inhibitor of eukaryotic initiation factor 4e (eIF4e), exhibiting noteworthy potential for investigating eIF4e dependent diseases, particularly cancer research (WO2021003157A1, compound 485).
价 格：￥电议型 号：T40210产 地：中国大陆
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T39921eIF4A3-IN-7eIF4A3-IN-7eIF4A3-IN-7
eIF4A3-IN-7 is a highly effective inhibitor of eIF4A3, exhibiting significant potential for research in cancer and dysproliferative diseases.
价 格：￥电议型 号：T39921产 地：中国大陆
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T39606CE3F4 analog 1；CE3F4 analog 1CE3F4 analog 1
CE3F4 analog 1 is an analogue of CE3F4.
价 格：￥电议型 号：T39606产 地：中国大陆
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T39530eIF4A3-IN-5eIF4A3-IN-5eIF4A3-IN-5
eIF4A3-IN-5 is a highly effective inhibitor of eukaryotic initiation factor 4A (eIF4A), specifically targeting eIF4AI and eIF4AII. With its potent inhibitory properties, eIF4A3-IN-5 shows great potential for advancing research in eIF4A-dependent diseases, including cancer studies.
价 格：￥电议型 号：T39530产 地：中国大陆
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T38129Leukotriene F4；Leukotriene F4LTF4；LTF4
LTF4 is a cysteinyl-leukotriene produced in vitro, but not reported to date in vivo. It is formed by the incubation of LTE4 with γ-glutamyl transpeptidase and glutathione. LTF4 is a weak agonist in its ability to contract vascular smooth muscle. [1] The rank order of potency of the cysteinyl-leukotrienes to contract vascular smooth muscle is LTD4 > LTC4 > LTE4 >> LTF4. [1] [2]
价 格：￥电议型 号：T38129产 地：中国大陆
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T35083VUF 4904；化合物 T35083VUF-4904|||VUF4904；VUF-4904|||VUF4904
VUF 4904 is a bioactive chemical.
价 格：￥电议型 号：T35083产 地：中国大陆
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T3430PF-4136309；化合物PF4136309INCB8761|||PF 4136309；INCB8761|||PF 4136309
PF-4136309 (INCB8761) is a specific, effective, and orally bioavailable CCR2 antagonist.
价 格：￥电议型 号：T3430产 地：中国大陆
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T33943PF-04856264化合物 T33943PF-4856264|||PF4856264|||PF 4856264
PF-04856264 is a potent and selective human Nav1.7 voltage-gated sodium channel inhibitor (IC50 = 28 nM).
价 格：￥电议型 号：T33943产 地：中国大陆
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T32681Leukotriene F-4 sulfone；化合物 T32681Ltf4 sulfone；Ltf4 sulfone
Leukotriene F-4 sulfone induces vascular permeability changes.
价 格：￥电议型 号：T32681产 地：中国大陆
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T31594EA-230；化合物 T31594EA 230|||NMPF-46|||NMPF46|||NMPF 46；EA 230|||NMPF-46|||NMPF46|||NMPF 46
Ea-230 is an immunomodulator that may be used in the treatment of renal failure.
价 格：￥电议型 号：T31594产 地：中国大陆
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T31008Copper probe CF4；化合物 Copper probe CF4Copper probe CF-4|||Copper probe CF 4|||Copper fluor CF4|||CF4
Copper probe CF4 (Copper fluor CF4) is a fluorescent copper probe that can be used to study colon cancer.
价 格：￥电议型 号：T31008产 地：中国大陆
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T304810058-F4；化合物10058-F4c-Myc Inhibitor；c-Myc Inhibitor
10058-F4 (c-Myc Inhibitor) is a cell-permeable thiazolidinone that specifically inhibits the c-Myc-Max interaction and prevents transactivation of c-Myc target gene expression; induces cell-cycle arrest and apoptosis.
价 格：￥电议型 号：T3048产 地：中国大陆
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T29543ACAF4；化合物 T29543ACAF-4|||ACAF 4；ACAF-4|||ACAF 4
ACAF4 is a neurotrophic agent which significantly increases survival in PC12 neuronal cells and enhances the effect of nerve growth factor (NGF). ACAF4 induces neurite outgrowth, and modulates ERK1/2 and AKT signaling pathways.
价 格：￥电议型 号：T29543产 地：中国大陆
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T28476Pyrroxamycin；化合物 T28476LL-F42248-alpha|||Dioxapyrrolomycin|||AL-R2081；LL-F42248-alpha|||Dioxapyrrolo
Pyrroxamycin is a new antibiotic. Pyrroxamycin was isolated from the culture broth of Streptomyces sp. S46506. Pyrroxamycin is active against Gram-positive bacteria and dermatophytes.
价 格：￥电议型 号：T28476产 地：中国大陆
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T28387PF-4950834；化合物 T28387PF 4950834|||PF4950834；PF 4950834|||PF4950834
PF-4950834, a ATP-competitive, selective Rho kinase inhibitor, provides therapeutic benefits in chronic inflammatory diseases.
价 格：￥电议型 号：T28387产 地：中国大陆
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T28367PF-04822163；化合物PF-04822163PF-4822163|||PF 04822163|||PF4822163|||PF04822163|||PF 4822163；PF-4822163|
PF-04822163 is a potent inhibitor of PDE1 with IC50 value of 0.0024 μM.
价 格：￥电议型 号：T28367产 地：中国大陆
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T28366PF-04628935；化合物 T28366PF 04628935|||PF 4628935|||PF4628935|||PF04628935|||PF-4628935；PF 04628935|||P
PF-04628935 is a potent antagonist/inverse agonist of the ghrelin receptor, growth hormone secretagogue receptor 1a (GHS-R1a) with an IC50 of 4.6 nM. PF-04628935 is orally bioavailable and brain penetrant.
价 格：￥电议型 号：T28366产 地：中国大陆
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T28360PF-00489791；化合物PF-00489791PF-4634817|||PF 4634817|||PF00489791|||PF 00489791|||PF4634817；PF-4634817|
PF-00489791 (PF4634817) is a long-acting PDE5 inhibitor with hypotensive activity for the study of diabetic nephropathy.
价 格：￥电议型 号：T28360产 地：中国大陆
