T322316beta-Methyl-16alpha,17alpha-epoxypregnenolone

价 格：￥电议型 号：T3223产 地：中国大陆

T2353BRD7116BRD7716

BRD7116 competitively binds to bacterial DNA gyrase, with cell-non-autonomous anti-leukemia activity.

价 格：￥电议型 号：T2353产 地：中国大陆

T1884CX516BDP 12；Ampakine CX516；Ampalex；安帕来斯

Ampalex (Ampakine CX516; CX516; BDP 12), an ampakine and nootropic, acts as an AMPA receptor positive allosteric modulator as a therapy for Alzheimer´s disease, schizophrenia and mild cognitive impairment (MCI).

价 格：￥电议型 号：T1884产 地：中国大陆

T2353BRD7716BRD7716,BRD7116,

BRD7116 competitively binds to bacterial DNA gyrase, with cell-non-autonomous anti-leukemia activity.

价 格：￥电议型 号：T2353产 地：美洲

T82910Bcl-2-IN-16；化合物 Bcl-2-IN-16Bcl-2-IN-16

Bcl-2-IN-16 is a Bcl-2 (B-cell lymphoma 2) inhibitor [1].

价 格：￥电议型 号：T82910产 地：中国大陆

T79830B-Raf IN 16；B-Raf 抑制剂 16B-Raf IN 16

B-Raf IN 16, a BRAF inhibitor, belongs to cyclic iminopyrimidine derivatives and can be used for cancer or tumour research.

价 格：￥电议型 号：T79830产 地：中国大陆

T78989BET-IN-16；化合物 BET-IN-16BET-IN-16

BET-IN-16 (Comp I), a bromodomain and extra-terminal (BET) inhibitor, demonstrates anticancer activity by impeding the growth of prostate cancer cells. It exhibits potent inhibitory effects with half-maximal inhibitory concentration (IC50) values of 0.043 μM for LNCaP cells and 0.034 μM for 22Rv1 cells [1].

价 格：￥电议型 号：T78989产 地：中国大陆

T78695BChE-IN-16；化合物 BChE-IN-16BChE-IN-16

BChE-IN-16 (compound 87) is a potent inhibitor of human butyrylcholinesterase (hBChE) exhibiting an inhibition concentration half-maximum (IC50) of 3.8 nM. It demonstrates low cytotoxicity and potential for central nervous system (CNS) permeability, along with unique adaptability, rendering it a valuable tool for research into Alzheimer´s disease (AD).

价 格：￥电议型 号：T78695产 地：中国大陆

T74879306-N16B；化合物 306-N16B306-N16B

306-N16B is a lipid nanoparticle designed for the systemic co-delivery of Cas9 mRNA and sgRNA, facilitating the transport of mRNA to pulmonary endothelial cells. This compound is advantageous for research focused on genome editing-based therapies [1].

价 格：￥电议型 号：T74879产 地：中国大陆

T73830BRD4 Inhibitor-16；化合物 BRD4 Inhibitor-16BRD4 Inhibitor-16

BRD4 Inhibitor-16 (Compound 4) is a potent inhibitor of bromodomain 4 (BRD4), whose overexpression is closely correlated with various human cancers through the regulation of histone post-translational modifications. It serves as a valuable tool for explorative studies focused on BRD4 inhibition, facilitating an enhanced comprehension of BRD4 inhibitor release-related information [1].

价 格：￥电议型 号：T73830产 地：中国大陆

T71265BMS-830216；化合物 BMS-830216BMS-830216

BMS-830216 is a nonbasic melanin hormone receptor 1 antagonist and a prodrug of BMS-819881.

价 格：￥电议型 号：T71265产 地：中国大陆

T71050U 80816B；化合物 U 80816BU 80816B

U 80816B is a cholinergic direct agonist.

价 格：￥电议型 号：T71050产 地：中国大陆

T68353BVT-74316；化合物 BVT-74316BVT-74316

BVT-74316 is an orally administered antagonist of the serotonin 6 receptor (5-HT6) being developed by Proximagen

价 格：￥电议型 号：T68353产 地：中国大陆

T66654(2b,3a,5a,16b,17b)-17-Acetoxy-3-hydroxy-2-(4-morpholinyl)-16-(1-pyrrolidinyl)androstane；化合物 (2b,3a,5

(2b,3a,5a,16b,17b)-17-Acetoxy-3-hydroxy-2-(4-morpholinyl)-16-(1-pyrrolidinyl)androstane is a useful organic compound for research related to life sciences. The catalog number is T66654 and the CAS number is 119302-24-8.

价 格：￥电议型 号：T66654产 地：中国大陆

T66653(2b,3a,5a,16b,17b)-2-(4-Morpholinyl)-16-(1-pyrrolidinyl)androstane-3,17-diol；化合物 (2b,3a,5a,16b,17b)-

(2b,3a,5a,16b,17b)-2-(4-Morpholinyl)-16-(1-pyrrolidinyl)androstane-3,17-diol is a useful organic compound for research related to life sciences and the catalog number is T66653.

价 格：￥电议型 号：T66653产 地：中国大陆

T61455BSP16；化合物 BSP16BSP16

BSP16 is a highly potent and orally active STING agonist, capable of selectively stimulating the interferon genes pathway. This compound, BSP16, holds great potential for cancer research [1].

价 格：￥电议型 号：T61455产 地：中国大陆

T60542BTK-IN-16；BTK抑制剂16BTK-IN-16

BTK-IN-16 is a potential inhibitor of wild-type BTK and C481S mutants.BTK-IN-16 can be used to study various autoimmune diseases and cancers caused by BTK.

价 格：￥电议型 号：T60542产 地：中国大陆

T40903ACG416B；ACG416BACG416B

ACG416B (compound 18) exhibits formidable inhibitory effects on choline kinase (ChoK), with an IC 50 measurement of 0.4 μM. Notably, ACG416B demonstrates superior inhibitory activities against HT-29 human colon cancer cells, resulting in pronounced antiproliferative effects.

价 格：￥电议型 号：T40903产 地：中国大陆

T40153BAMEA-O16B；BAMEA-O16BBAMEA-O16B；BAMEA-O16B

BAMEAO16B is a lipid nanoparticle that incorporates disulfide bonds for efficient delivery of Cas9 mRNA and sgRNA into cells. In the intracellular environment, BAMEAO16B responds to reduction by releasing RNA, facilitating genome editing. This compound is valuable for gene editing research purposes.

价 格：￥电议型 号：T40153产 地：中国大陆

T378116-Chloro-3-indolyl-β-D-Glucuronide CHA；6-Chloro-3-indolyl-β-D-Glucuronide 环已胺盐16beta-Methyl-16alpha,

6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) is a chromogenic substrate for β-glucuronidase. 6-Chloro-3-indolyl-β-D-Glucuronide (cyclohexylammonium salt) can be used in the histochemical analysis of β-glucuronidase activity.

价 格：￥电议型 号：T37811产 地：中国大陆