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T27491GSK730；化合物 T27491GSK730
GSK730 is an inactive enantiomer of GSK729 (GLXC-09258).
价 格：￥电议型 号：T27491产 地：中国大陆
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T27471GSK299115A；化合物GSK299115AGSK 299115A|||GSK-299115A；GSK 299115A|||GSK-299115A
GSK299115A (GSK-299115A) is a selective ROCK1 Inhibitor. GSK299115A exhibits IC50 of 8nM, 620nM, 560nM for ROCK1, RSK1, p70S6K, respectively.
价 格：￥电议型 号：T27471产 地：中国大陆
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T27461GSK2336805；化合物 T27461GSK 2336805|||GSK-2336805|||JNJ-56914845|||GSK-805|||GSK805；GSK 2336805|||GSK-2
GSK-2336805 is a HCV NS5A inhibitor. GSK2336805 retained activity on chimeric replicons containing NS5A patient sequences from genotype 1 and patient and consensus sequences for genotypes 4 and 5 and part of genotype 6.
价 格：￥电议型 号：T27461产 地：中国大陆
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T27433GRI918013；化合物 T27433GRI 918013|||GRI-918013；GRI 918013|||GRI-918013
GRI918013 is an ATX inhibitor.
价 格：￥电议型 号：T27433产 地：中国大陆
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T27399Galocitabine；加洛他滨RO 091390|||RO-091390|||RO091390|||RO-09-1390|||Neofrutulon；RO 091390|||RO-091390||
Galocitabine (Neofrutulon), a thymidylate synthase inhibitor, is used potentially for the treatment of cancer.
价 格：￥电议型 号：T27399产 地：中国大陆
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T27337Floxacrine；化合物 T27337HOE-991|||HOE 991|||HOE991；HOE-991|||HOE 991|||HOE991
Floxacrine is drug candidate for chemoprophylaxis of malaria.
价 格：￥电议型 号：T27337产 地：中国大陆
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T27237Echinocandin B；化合物 T27237A-30912A|||NSC 287461|||A 30912A|||A30912A|||A22082；A-30912A|||NSC 287461||
Echinocandin B is a cyclic hexapeptide echinocandin antibiotic from Aspergillus nidulans var. echinulatus . It attacks the cell wall of fungi by inhibiting beta-1,3-glucan synthesis.
价 格：￥电议型 号：T27237产 地：中国大陆
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T27191D-Mannuronic Acid；化合物 T27191D-Mannuronic Acid
D-Mannuronic Acid is a blocker of the TLR2 and TLR4 downstream signaling pathway. D-Mannuronic Acid effectively inhibits mRNA expression of MyD88 and p65, major subunit of nuclear factor-kappaB.
价 格：￥电议型 号：T27191产 地：中国大陆
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T27091Cryptopleurine；化合物 T27091NSC-19912|||NSC 19912|||NSC19912；NSC-19912|||NSC 19912|||NSC19912
Cryptopleurine is an inhibitor of gene products associated with cell proliferation, survival, invasion and angiogenesis. It acts by targeting the NF-κB pathway.
价 格：￥电议型 号：T27091产 地：中国大陆
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T27081CRA-19156；化合物 T27081CRA19156；CRA19156
CRA-19156 is a potent HDAC8 inhibitor.
价 格：￥电议型 号：T27081产 地：中国大陆
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T27037CL-329167；化合物 T27037CL329167|||CL 329167；CL329167|||CL 329167
CL-329167, a angiotensin type 1 receptor antagonist, is used potentially for the treatment of hypertension.
价 格：￥电议型 号：T27037产 地：中国大陆
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T26955Cavosonstat；卡伏索司他N91115|||N 91115|||N-91115；N91115|||N 91115|||N-91115
Cavosonstat (N91115) is an orally active S-nitrosoglutathione reductase (GSNOR) inhibitor that promotes cystic fibrosis transmembrane conductance regulator (CFTR) maturation and plasma membrane stabilization.Cavosonstat is a CFTR stabilizer and can be used to study cystic fibrosis.
价 格：￥电议型 号：T26955产 地：中国大陆
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T26919BU09059；化合物 T26919BU 09059|||BU-09059；BU 09059|||BU-09059
BU09059 is a potent, selective, short-acting antagonist of the κ-opioid receptor (KOR).
价 格：￥电议型 号：T26919产 地：中国大陆
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T26918BU08028；化合物 T26918BU 08028|||BU-08028；BU 08028|||BU-08028
BU08028 is a mu opioid peptide (MOP) receptor and nociceptin-orphanin FQ peptide (NOP) receptor agonist.
价 格：￥电议型 号：T26918产 地：中国大陆
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T26917BTT-3033；化合物 BTT-3033BTT3033|||BTT 3033；BTT3033|||BTT 3033
BTT-3033 is an orally active and potent α2β1 (EC50: 130 nM) inhibitor with an EC50 value of 130 nM. BTT-3033 has an affinity for the α2I domain and inhibits platelet binding to collagen I and cell proliferation.BTT-3033 induces apoptosis and can be used in the study of prostate cancer, BTT-3033 induces apoptosis and can be used to study prostate cancer, inflammation and cardiovascular disease.
价 格：￥电议型 号：T26917产 地：中国大陆
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T26916BTI-A-404；化合物 T26916BTI-A-404
BTI-A-404 is a potent and selective competitive inverse agonist of human GPR43.
价 格：￥电议型 号：T26916产 地：中国大陆
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T26915BTG-1640；化合物 T26915ABIO-0801|||ABIO-08-01|||SP-1640；ABIO-0801|||ABIO-08-01|||SP-1640
BTG-1640 is used potentially for the treatment of anxiety and panic disorder.
价 格：￥电议型 号：T26915产 地：中国大陆
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T26914L(R)-AZD 9639；化合物 (R)-AZD 9639(R)-AZD 9639
(R)-AZD 9639 is the R-isomer of AZD 9639, a novel respiratory syncytial virus (RSV) fusion inhibitor with antiviral activity.
价 格：￥电议型 号：T26914L产 地：中国大陆
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T26914BTA-9881；化合物 BTA-9881BTA9881|||AZD9639|||AZD-9639|||BTA 9881|||MEDI-564；BTA9881|||AZD9639|||AZD-9639
BTA-9881 is a novel RSV fusion inhibitor with oral activity and antiviral activity for the study of respiratory syncytial virus infections.
价 格：￥电议型 号：T26914产 地：中国大陆
