T86121-Methyl-2-(Methylthio)iMidazole1Methyl2(Methylthio)iMidazole,1 Methyl 2 (Methylthio)iMidazole

1-Methyl-2-(methylthio)imidazole is an impurity of Methimazole, a thiourea antithyroid agent that prevents iodine organification, thus inhibiting the synthesis of thyroxine.

价 格：￥电议型 号：T8612产 地：中国大陆

TN24364-methyl-6-phenyl-2H-pyranone

4-methyl-6-phenyl-2H-pyranone is derived from Scutellaria baicalensis Georgi and improves mitochondrial functionality to protect astrocytes against hydrogen peroxide-induced toxicity.

价 格：￥电议型 号：TN2436产 地：中国大陆

TN2069PicrocrocinInhibitor,Picrocrocin,antiproliferative,SKMEL-2,Apoptosis,malignant,melanoma,cells,human,

Picrocrocin is a natural product

价 格：￥电议型 号：TN2069产 地：中国大陆

T93325-Pyrimidinecarboxamide, 2-[[(1R,2S)-2-aminocyclohexyl]amino]-4-[[3-(2H-1,2,3-triazol-2-yl)phenyl]am

5-Pyrimidinecarboxamide, 2-[[(1R,2S)-2-a is a chemical compound.

价 格：￥电议型 号：T9332产 地：中国大陆

T8375ML-210residue,Ferroptosis,inhibit,peroxidase,ML-210,Covalent,selenocysteine,Glutathione Peroxidase,M

ML-210 is a selective RAS and covalent glutathione peroxidase 4 (GPX4) inhibitor(GPX4, EC50 : 30 nM), with anti-cancer activity

价 格：￥电议型 号：T8375产 地：中国大陆

T82643-Methyl-2-oxovaleric acid3 Methyl 2 oxovaleric acid,inhibit,3Methyl2oxovaleric acid,Endogenous Meta

3-Methyl-2-oxovaleric acid is an abnormal metabolite that arises from the incomplete breakdown of branched-chain amino acids. 3-Methyl-2-oxovaleric acid is a neurotoxin, an acidogen, and a metabotoxin. A neurotoxin causes damage to nerve cells and nerve tissues.

价 格：￥电议型 号：T8264产 地：中国大陆

T60023CL-278474CL278474,CL 278474

CL-278474 (compound I-79) is a potent inhibitor of β-N-acetylhexosaminidase OfHex1. CL-278474 can be used in control of insect.

价 格：￥电议型 号：T60023产 地：中国大陆

T60205(2S)-4-biphenyl-4-yl-N-hydroxy-2-methyl-2-(methylsulfonyl)butanamide(2S)4biphenyl4ylNhydroxy2methyl2

(2S)-4-biphenyl-4-yl-N-hydroxy-2-methyl-2-(methylsulfonyl)butanamide is a LpxC inhibitor with IC50 >95.2 nM.

价 格：￥电议型 号：T60205产 地：中国大陆

T6778BDA-366Inhibitor,BDA-366,Antitumor,Bcl-2 Family,inhibit,Bcl2-BH4 domain,Anticancer,BDA 366,Antiapopt

BDA-366 is a potent Bcl2 antagonist, binding Bcl2-BH4 domain with high affinity and selectivity (Ki = 3.3 nM). BDA-366 induces conformational change in Bcl2 that abrogates its antiapoptotic function, converting it from a survival molecule to a cell death inducer. BDA-366 suppresses growth of lung cancer cells[1].

价 格：￥电议型 号：T6778产 地：中国大陆

Fr212652-Methyl-2H-indazole-3-carboxylic acid

价 格：￥电议型 号：Fr21265产 地：中国大陆

T9945MNK8?MNK-8,HepG2,Bcl-2 Family,STAT3 inhibitor,inhibit,MNK8,MNK8?,Antimigratory agent,Inhibitor,STAT,

3-methyl-6- (naphthalen-1-yl)pyrimidine-2,4(1H, 3H)-dione is a potent STAT3 inhibitor that reduces the ability of STAT3 to bind to DNA and also has a good growth inhibition effect on liver cancer cells [1].

价 格：￥电议型 号：T9945产 地：中国大陆

T9608KL201KL201,CRY1,Inhibitor,Per2-dLuc,FBXL3,inhibit,clock,KL 201,circadian,cryptochrome,KL-201

KL201 a circadian clock modulator, is a isoform-selective cryptochrome 1 (CRY1) stabilizer. KL201 lengthens the period of circadian rhythms in cells and tissues[1].

价 格：￥电议型 号：T9608产 地：中国大陆

T9493DL-2-AMINOOCTANOIC ACIDDL2AMINOOCTANOIC ACID,DL 2 AMINOOCTANOIC ACID

DL-2-Aminooctanoic acid, also known as a-aminocaprylate or alpha-aminocaprylic acid, belongs to the class of organic compounds known as alpha-amino acids.

价 格：￥电议型 号：T9493产 地：中国大陆

T6S0052ChelerythrineBcl-2 Family,Apoptosis,Protein kinase C,PKC,Inhibitor,Chelerythrine,inhibit,Autophagy

1. Chelerythrine may have antimanic effect . 2. Chelerythrine can inhibit telomerase activity. 3. Chelerythrine is a well-known protein kinase C inhibitor . 4. Chelerythrine has potential antiproliferative and antitumor effects.

价 格：￥电议型 号：T6S0052产 地：中国大陆

T8974ML-211MAGL,ML 211,inhibit,Phospholipase,Monoacylglycerol lipase,ML-211,Inhibitor,ML211

ML-211 is a carbamate-based dual inhibitor of LYPLA1 (IC50 = 17 nM) and the related LYPLA2 (IC50 = 30 nM)

价 格：￥电议型 号：T8974产 地：中国大陆

T6748A-1155463Bcl-2 Family,Inhibitor,A-1155463,inhibit

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

T67754(3Z)-5-(pyridin-3-yl)-3-[(1H-pyrrol-2-yl)methylidene]-2,3-dihydro-1H-indol-2-one(3Z)5(pyridin3yl)3[(

(3Z)-5-(pyridin-3-yl)-3-[(1H-pyrrol-2-yl)methylidene]-2,3-dihydro-1H-indol-2-one is a potent, selective and orally active FLT3 inhibitor, with IC50s of ?40, 8, and 4 nM for FLT3-WT, FLT3-D835Y, and FLT3-D835H, respectively.

价 格：￥电议型 号：T67754产 地：中国大陆

T10833CL264CL264,CL-264

CL264, a selective agonist of TLR7, can be used in studies about innate immune signals.

价 格：￥电议型 号：T10833产 地：中国大陆

T6749A-1331852A-1331852,Inhibitor,inhibit,A1331852,Bcl-2 Family,A 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

T6894ML264ML-264,Inhibitor,Krüppel-like factor,ML 264,inhibit,ML264,KLF

ML264 is a selective kruppel-like factor 5 (KLF5) inhibitor, which potently Inhibits growth of Colorectal Cancer.

价 格：￥电议型 号：T6894产 地：中国大陆