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T4136Lapachol黄钟花醌；Greenhartin；CI75490；Tecomin；Bethabarra wood
Lapachol has antimicrobial properties against many pathogens. It has anti-inflammatory, analgesic and antibiotic properties. It is an inhibitor of epithelial tumors in Drosophila melanogaster heterozygote.
价 格：￥电议型 号：T4136产 地：中国大陆
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T40490PhenylalanylalanineH-Phe-Ala-OH；Phenylalanylalanine
Phenylalanylalanine (H-Phe-Ala-OH) is a dipeptide composed of phenylalanine and alanine. Phenylalanylalanine is an incomplete breakdown product of protein digestion or protein catabolism [1] .
价 格：￥电议型 号：T40490产 地：中国大陆
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T3454VER-49009CCT 129397
VER-49009 is a potent Hsp90 inhibitor(IC50 of 25 nM and Kd of 78 nM).
价 格：￥电议型 号：T3454产 地：中国大陆
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T3274S49076
S49076 is a novel, potent inhibitor of MET, AXL/MER, and FGFR1/2/3, blocking cellular phosphorylation of MET, AXL, and FGFRs.
价 格：￥电议型 号：T3274产 地：中国大陆
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T2S0490Eugenol acetate乙酰丁香酚；乙酸丁香酚酯；1,3,4-Eugenol acetate；Acetyleugenol；Aceteugenol；Eugenyl acetate
Eugenol Acetate is a constituent of Clove oil, an essential oil from the clove plant, Syzygium aromaticum. Clove oil is a natural analgaesic and antiseptic used primarily in dentistry for its main ingredient Eugenol. Clove oil can also be purchased in pha
价 格：￥电议型 号：T2S0490产 地：中国大陆
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T2600AG490AG 490；Tyrphostin B42；AG-490；Zinc02557947；Tyrphostin AG 490
AG-490 (Tyrphostin AG 490) is an inhibitor of EGFR (IC50: 0.1 μM). It is 135-fold more selective for EGFR than ErbB2, also inhibits JAK2 with no effect to Lyn, Lck, Syk, Btk, and Src.
价 格：￥电议型 号：T2600产 地：中国大陆
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T2490OsimertinibMereletinib；AZD-9291；奥希替尼
Osimertinib is a small molecule tyrosine kinase receptor inhibitor and antineoplastic agent that is used in the therapy of selected forms of advanced non-small cell lung cancer (NSCLC).
价 格：￥电议型 号：T2490产 地：中国大陆
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T2268VER49009VER 49009；CCT0129397；VER-49009
VER-49009 is an effective HSP90 inhibitor(IC50 =25 nM, Kd=78 nM).
价 格：￥电议型 号：T2268产 地：中国大陆
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T22339GNE-490
GNE-490 is an effective inhibitor of pan-PI3K with IC50s of 3.5 nM, 25 nM, 5.2 nM, 15 nM for PI3Kα, PI3Kβ, PI3Kδ and PI3Kγ, respectively. GNE-490 has >200 fold selectivity for mTOR (IC50 = 750 nM).
价 格：￥电议型 号：T22339产 地：中国大陆
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T21957Guanabenz hydrochlorideNE56490
Guanabenz hydrochloride is an orally active α2-adrenoceptor agonist with hypotensive effects.
价 格：￥电议型 号：T21957产 地：中国大陆
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T2179TriptolidePG490；NSC 163062；雷公藤甲素
Triptolide is a diterpenes trioxide, immunosuppressive agent extracted from the Chinese herb Tripterygium wilfordii.
价 格：￥电议型 号：T2179产 地：中国大陆
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T14920CE-224535PF-04905428
CE-224535 is a selective antagonist of P2X7 receptor. CE-224535 can be used in disease-modifying antirheumatic studies.
价 格：￥电议型 号：T14920产 地：中国大陆
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T14909CCX140CCX140-B；3-三氟甲基-4-氯-N-[2-[7H-吡咯并[2,3-D]嘧啶-4-羰基]-5-甲基-3-吡啶基]苯磺酰胺
CCX140 (CCX140-B) is an antagonist of CCR2.
价 格：￥电议型 号：T14909产 地：中国大陆
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T14907CCT251545
CCT251545 is an potent and oral-bioavailable WNT signaling inhibitor(IC50 of 5 nM in 7dF3 cells).
价 格：￥电议型 号：T14907产 地：中国大陆
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T14901CCT-251921
CCT-251921 is a potent, selective, and orally bioavailable CDK8 inhibitor (IC50: 2.3 nM).
价 格：￥电议型 号：T14901产 地：中国大陆
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T14900CCR2-RA-[R](5R)-4-乙酰基-1-(4-氯-2-氟苯基)-5-环己基-1,5-二氢-3-羟基-2H-吡咯-2-酮
CCR2-RA-[R] is a C-C chemokine receptor type 2 (CCR2) allosteric antagonist (IC50: 103 nM).
价 格：￥电议型 号：T14900产 地：中国大陆
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T1490GestodeneSHB 331；WL 70；孕二烯酮
Gestodene is a progestogen hormonal contraceptive.
价 格：￥电议型 号：T1490产 地：中国大陆
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T1484LPerindopril erbumine培哚普利叔丁胺；培哚普利叔丁胺盐；S9490-3；Perindopril tert-butylamine salt
Perindopril Erbumine is the tert-butylamine salt of perindopril, the ethyl ester of a non-sulfhydryl angiotensin-converting enzyme (ACE) inhibitor with antihypertensive activity. Upon hydrolysis, perindopril erbumine is converted to its active form perind
价 格：￥电议型 号：T1484L产 地：中国大陆
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T14490Talipexole dihydrochloride盐酸他利克索；Domnin；B-HT 920 dihydrochloride
Talipexole dihydrochloride is a dopamine D2 receptor agonist, α2-adrenoceptor agonist, and 5-HT3 receptor antagonist in both rat cortical and intestinal membrane fractions with Ki values of 0.35 μM and 0.22 μM, respectively. It displays antiParkinsonian a
价 格：￥电议型 号：T14490产 地：中国大陆
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T14327AS1949490
AS1949490 activated glucose metabolism via up-regulation of GLUT1 gene in L6 myotubes[1][2]. AS1949490 is a potent and selective SHIP-2 (SH2 domain-containing inositol 5′ phosphatase 2) inhibitor, with an IC50 of 620 nM.
价 格：￥电议型 号：T14327产 地：中国大陆
