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结构式 货号 产品名称 CAS号
2,3-Diazabicyclo[3.1.1]heptane-4-carboxylic acid, methyl ester, (4S)- 结构式
BCP49700 2,3-Diazabicyclo[3.1.1]heptane-4-carboxylic acid, methyl ester, (4S)- 3034241-21-6
Mutated EGFR-IN-1 结构式
BCP28639 Mutated EGFR-IN-1 1421372-66-8
Mutated EGFR-IN-1 is a useful intermediate for the inhibitors design for mutated EGFR, such as L858R EGFR, Exonl9 deletion activating mutant and T790M resistance mutant.
Sevabertinib 结构式
BCP49699 Sevabertinib 2521285-05-0
Sevabertinib is an epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor with antitumor activity.
CMP-5 dihydrochloride 结构式
BCP49698 CMP-5双盐酸盐 2309409-79-6
CMP-5 hydrochloride is a potent and selective PRMT5 inhibitor, while displays no activity against PRMT1/4/7 enzymes. It selectively blocks S2Me-H4R3 by inhibiting PRMT5 methyltransferase activity on histone preparations.
CBD3063 结构式
BCP49697 CBD3063 1281060-70-5
CBD3063 is a selective, first-in-class, CRMP2-based peptidomimetic small molecule, which allosterically regulates Cav2.2 to achieve analgesia and pain relief without negative side effect profiles.
Pogostone 结构式
BCP49696 广藿香酮 23800-56-8
Pogostone is isolated from mint and has antibacterial and anticancer activities. Pogostone inhibited gram-negative bacteria and Gram-positive bacteria, and also showed inhibitory effect on Bacillus sclericae, with MIC value of 0.098 µg/mL. Pogostone can induce apoptosis and autophagy.
(2S)-2-cyclopentyl-2-[(5S)-2-[(2-methylpropan-2-yl)oxycarbonyl]-2,7-diazaspiro[4.4]nonan-7-yl]acetic acid 结构式
BCP49694 (2S)-2-cyclopentyl-2-[(5S)-2-[(2-methylpropan-2-yl)oxycarbonyl]-2,7-diazaspiro[4.4]nonan-7-yl]acetic acid 2865128-45-4
Tafluprost 16 E-diene 结构式
BCP49695 他氟前列素 16 E-二烯 T16ED
Cefixime Dimer D 结构式
BCP49693 头孢克肟二聚体D CDD
(S)-3-[(S)-4-Boc-吗啉-2-基]-2-(Cbz-氨基)丙酸甲酯 结构式
BCP49692 (S)-3-[(S)-4-Boc-吗啉-2-基]-2-(Cbz-氨基)丙酸甲酯 2641824-60-2
5-Bromo-3-(3-((tert-butyldiphenylsilyl)oxy)-2,2-dimethylpropyl)-2-iodo-1H-indole 结构式
BCP49691 5-溴-3-(3-((叔丁基二苯基甲硅烷基)氧基)-2,2-二甲基丙基)-2-碘-1H-吲哚 2641451-43-4
KRAS G12D inhibitor 18 结构式
BCP49689 KRAS G12D inhibitor 18 2922732-54-3
KRAS G12D inhibitor 18 is a potent KRAS G12D inhibitor.
Tromethamine hydrochloride 结构式
BCP49690 三羟甲基氨基甲烷盐酸盐 1185-53-1
Trometamol hydrochloride is a biologically inert amino alcohol of low toxicity, which buffers carbon dioxide and acids in vitro and in vivo. Trometamol hydrochloride is an effective amine compound for pH control in the physiological range.
3-Aminobenzaldehyde 结构式
BCP21987 间氨基苯甲醛 1709-44-0
Pretomanid 结构式
BCP21111 普托马尼 187235-37-6
PA-824 is an experimental anti-tuberculosis drug and one of two nitroimidazoles in phase II clinical trials to treat tuberculosis.
Tafluprost Impurity 21 结构式
BCP43839 他氟前列腺素杂质 21 1563176-58-8
Lificiguat 结构式
BCP09072 利非西呱 170632-47-0
YC-1(Lificiguat) is a soluble guanylyl cyclase(sGC) activator; binds to the heme-containing domain of the β subunit with Kd value of 0.6-1.1 μM in the presence of CO.
CD1530 结构式
BCP28865 CD1530 107430-66-0
CD-1530 is a retinoic acid receptor γ selective agonist.
Exatecan Intermediate 6 结构式
BCP44295 Exatecan Intermediate 6 143655-58-7
Exatecan Intermediate 6 is the intermediate of Exatecan(DX-8951) which is a DNA topoisomerase I inhibitor with an IC50 value of 2.2 μM (0.975 μg/mL) that can be used in cancer research.
SB202190 结构式
BCP00675 SB202190 152121-30-7
SB 202190 is a highly selective, potent and cell-permeable inhibitor of p38 MAP kinase. SB202190 binds within the ATP pocket of the active kinase (Kd = 38 nM, as measured in recombinant human p38), and selectively inhibits the p38α and β isoforms (IC50 = 50 and 100 nM at SAPK2a/p38 and SAPK2b/p38β2 respectively).
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