Tyrosine Kinase(酪氨酸激酶)
- Bcr-Abl(70)
- Ack1(2)
- Axl(6)
- ALK(61)
- BMX Kinase(3)
- Broad Spectrum Protein Kinase Inhibitor(10)
- c-FMS(41)
- c-Kit(57)
- c-MET(92)
- c-RET(7)
- CSF-1R(3)
- DDR1/DDR2 Receptor(1)
- EGFR(266)
- EphB4(1)
- FAK(39)
- FGFR(103)
- FLT3(91)
- HER2(15)
- IGF1R(34)
- Insulin Receptor(45)
- IRAK(32)
- ITK(10)
- Lck(1)
- LRRK2(24)
- PDGFR(107)
- PTKs/RTKs(9)
- Pyk2(8)
- ROR(41)
- Spleen Tyrosine Kinase (Syk)(33)
- Src(101)
- Tie-2 (4)
- Trk(43)
- VEGFR(193)
- Discoidin Domain Receptor(16)
- DYRK(33)
- Ephrin Receptor(13)
- RET(29)
- ROS(14)
- TAM Receptor(32)
- IGFBR(1)
- Others(55)
- Cat.No. 产品名称 Information
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GC19330
SGI-7079
3-[2-[[3-氟-4-(4-甲基-1-哌嗪基)苯基]氨基]-5-甲基-7H-吡咯并[2,3-D]嘧啶-4-基]苯乙腈
An Axl kinase inhibitor -
GC19321
Savolitinib
赛沃替尼; Volitinib; HMPL-504; AZD-6094
An inhibitor of c-Met -
GC19317
S49076
S49076 是一种新型、有效的 MET、AXL/MER 和 FGFR1/2/3 抑制剂,IC50 值低于 20 nM。
-
GC19287
PF06650833
PF-06650833
PF06650833 (PF-06650833) 是一种有效的、选择性的和口服活性的白细胞介素 1 受体相关激酶 4 (IRAK4) 抑制剂,在细胞和 PBMC 试验中的 IC50 分别为 0.2 和 2.4 nM。 -
GC19279
PD-166866
A potent inhibitor of FGFR1
-
GC19256
MTX-211
Mol 211
MTX-211 (Mol 211) 是 EGFR 和 PI3K 的双重抑制剂,IC50 值 <100 nM。 MTX-211可用于癌症和其他疾病的研究。 -
GC19218
Lazertinib
YH25448; GNS-1480
An irreversible inhibitor of mutant EGFRs -
GC19205
JH-II-127
An inhibitor of wild-type and mutant forms of LRRK2
-
GC19187
H3B-6527
An FGFR4 inhibitor
-
GC19179
GSK2256098
A FAK inhibitor
-
GC19166
Glesatinib hydrochloride
MGCD265 hydrochloride
Glesatinib hydrochloride (MGCD265 hydrochloride) 是一种具有口服活性的强效 MET/SMO 双重抑制剂。 Glesatinib hydrochloride 是一种酪氨酸激酶抑制剂,可拮抗 P-糖蛋白 (P-gp) 介导的非小细胞肺癌 (NSCLC) 中的多药耐药 (MDR)。 -
GC19158
FLT3-IN-2
An inhibitor of FLT3, c-Kit, and c-FMS
-
GC19156
TAS-120
TAS-120
An orally bioavailable, irreversible inhibitor of FGFRs -
GC19155
FGFR4-IN-1
An inhibitor of FGFR4
-
GC19154
Roblitinib
8-二氮杂萘-1(2H)-甲酰胺,FGF-401
Roblitinib (FGF-401) 是一种 1,8-naphthyridine 吡啶衍生物。 -
GC19142
Erdafitinib
厄达替尼; JNJ-42756493
A pan-FGFR inhibitor -
GC19140
X-376
恩沙替尼
An ALK inhibitor -
GC19132
EGFR-IN-3
EGFR-IN-3 是第三代 EGFR TKI,GI50 值分别为 5 nM (EGFR L858R/T790M)、10 nM (EGFR del19) 和 689 nM (EGFR WT)。 EGFR-IN-3 具有用于 NSCLC 研究的潜力。
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GC19108
SCR-1481B1
麦他替尼胺丁三醇,c-Met inhibitor 2
A pyridone -
GC19102
CEP-40783
RXDX-106
A multi-kinase inhibitor -
GC19092
CCT241736
A dual inhibitor of Aurora kinases and FLT3
-
GC19084
Brigatinib
布格替尼; AP-26113
An orally bioavailable ALK inhibitor -
GC19080
BPR1J-097
An FLT3 inhibitor
-
GC19075
BLU-554
BLU-554
A potent inhibitor of FGFR4 -
GC19074
Avapritinib
阿伐普替尼,BLU-285
A dual inhibitor of KIT and PDGFRα mutant kinases -
GC19066
BGB-283
BGB-283 is a novel and potent Raf Kinase and EGFR inhibitor with IC50 values of 23 and 29 nM for recombinant BRafV600E and EGFR, respectively.
-
GC19063
Belizatinib
TSR-011
An ALK inhibitor -
GC19062
BBT594
NVP-BBT594
BBT594 是一种有效的受体酪氨酸激酶 RET 抑制剂,用于癌症治疗。 -
GC19044
Avitinib maleate
艾维替尼马来酸盐; Abivertinib maleate; AC0010 maleate
A selective inhibitor of mutant EGFR -
GC18718
bpV(pic) (potassium hydrate)
Bisperoxovanadium(pic)
A PTEN inhibitor -
GC18591
GSK805
N-(2,6-二氯-2'-(三氟甲氧基)-[1,1'-联苯]-4-基)-2-(4-(乙基磺酰基)苯基)乙酰胺
An RORγt inverse agonist -
GC18580
B355252
A neuroprotective agent
-
GC18492
GSK3179106
RET Kinase Inhibitor 1
A RET kinase inhibitor -
GC18438
CGP 77675
An inhibitor of Src family kinases
-
GC18211
Ningetinib
宁格替尼
A multi-kinase inhibitor -
GC19012
(R)-GNE-140
(R)-3-((2-氯苯基)硫基)-4-羟基-6-(4-吗啉苯基)-6-(噻吩-3-基)-5,6-二氢吡啶-2(1H)-酮
(R)-GNE-140 是一种有效的乳酸脱氢酶 A (LDHA) 抑制剂,对 LDHA 和 LDHB 的 IC50 分别为 3 nM 和 5 nM; (R)-GNE-140 的效力是 S 对映体的 18 倍。 -
GC18168
JI-101
CGI1842
An inhibitor of VEGFR2, PDGFRβ, and EphB4 -
GC18167
AC710
N-[4-[[[[5-(叔丁基)-3-异恶唑基]氨基]羰基]氨基]苯基]-5-[(1-乙基-2,2,6,6-四甲基-4-哌啶基)氧基]-2-吡啶甲酰胺
A PDGFR family kinase inhibitor -
GC11737
AG957
NSC 654705,Tyrphostin AG957
An inhibitor of Bcr-Abl and c-Abl -
GC16235
AG-1295
酪氨酸磷酸化抑制剂AG1295,NSC 380341,Tyrphostin AG-1295
A selective inhibitor of PDGF receptor kinase -
GC12864
AG-1557
Tyrphostin AG-1557
An EGFR inhibitor -
GC15365
N-Acetylserotonin
N-乙酰-5-羟色胺,N-Acetyl-5-hydroxytryptamine,NAS
The immediate precursor of melatonin -
GC14951
Meleagrin
6-O-Methyloxaline
A Fabl inhibitor -
GC12461
HA-100 (hydrochloride)
C-1
An inhibitor of PKA, PKC, and PKG -
GC14890
AG-183
酪氨酸磷酸化抑制剂A51,Tyrphostin 51
An inhibitor of EGF receptor kinase -
GC12251
Tandutinib (MLN518) HCl
FLT3 inhibitor,potent and selective
-
GC13988
HNMPA
Hydroxy-2-naphthalenylmethyl Phosphonic Acid
An insulin receptor tyrosine kinase inhibitor -
GC11024
AG-213
酪氨酸磷酸化抑制剂,Tyrphostin AG-213,Tyrphostin 47
An inhibitor of EGF receptor kinase -
GC10217
RG-14620
Tyrphostin RG14620
An inhibitor of EGF receptor kinase -
GC11845
AG-82
酪氨酸磷酸化抑制剂25,NSC 676484,RG-50875,Tyrphostin 25,Tyrphostin AG-82
An inhibitor of EGF receptor kinase