当前位置：易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型：会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累，可浏览访问
(41-90)良好信誉积累，可接洽商谈
(91+ )优质信誉积累，可持续信赖
易推广会员：5年
工商认证 【已认证】
最后认证时间：
注册号： 【已认证】
法人代表： 【已认证】
企业类型：生产商 【已认证】
注册资金：人民币万 【已认证】
产品数：86101
参观次数：3779501
自主品牌
已选条件
-
-
T1242764-Deacetylneosolaniol；化合物 4-Deacetylneosolaniol4-Deacetylneosolaniol
4-Deacetylneosolaniol is a useful organic compound for research related to life sciences. The catalog number is T124276 and the CAS number is 74833-39-9.
价 格：￥电议型 号：T124276产 地：中国大陆
-
T124176Austalide B；化合物 Austalide BAustalide B
Austalide B is a useful organic compound for research related to life sciences. The catalog number is T124176 and the CAS number is 81543-02-4.
价 格：￥电议型 号：T124176产 地：中国大陆
-
T124076Aspergamide A；化合物 Aspergamide AAspergamide A
Aspergamide A is a useful organic compound for research related to life sciences. The catalog number is T124076 and the CAS number is 863238-39-5.
价 格：￥电议型 号：T124076产 地：中国大陆
-
T123976Helenalin tiglate；化合物 Helenalin tiglateHelenalin tiglate
Helenalin tiglate is a useful organic compound for research related to life sciences. The catalog number is T123976 and the CAS number is 89708-26-9.
价 格：￥电议型 号：T123976产 地：中国大陆
-
T12385PD0176078；化合物PD0176078PD176078；PD176078
PD0176078 () is a newly blocker of N-type Calcium channel.
价 格：￥电议型 号：T12385产 地：中国大陆
-
T12376PC945；化合物PC945Opelconazole；Opelconazole
PC945 (Opelconazole) is a potent broad-spectrum antifungal compound with inhibitory effect on fumonisinol 14α-demethylase (CYP51A/CYP51B), which can be used in the study of fungal infections of the lungs.
价 格：￥电议型 号：T12376产 地：中国大陆
-
T12276NVS-CRF38；化合物 T12276NVS-CRF38
NVS-CRF38 is an antagonist of corticotropin-releasing factor receptor 1 (CRF1).
价 格：￥电议型 号：T12276产 地：中国大陆
-
T12207NEO 376；化合物NEO 376SPI-376；SPI-376
NEO 376 (SPI-376) is a selective 5-HT1 receptor, GABA receptor and dopamine receptor modulator, showing anti-psychotic actively.
价 格：￥电议型 号：T12207产 地：中国大陆
-
T12200Firsocostat S enantiomer；化合物 T12200ND-630 S enantiomer|||NDI-010976 S enantiomer|||GS-0976 S enantio
Firsocostat S enantiomer is the less active S enantiomer of Firsocostat.
价 格：￥电议型 号：T12200产 地：中国大陆
-
T12176Naratriptan D3 Hydrochloride；化合物 T12176GR-85548A D3；GR-85548A D3
Naratriptan D3 Hydrochloride is the deuterium labeled Naratriptan, is a selective agonist of 5-HT1 receptor subtype.
价 格：￥电议型 号：T12176产 地：中国大陆
-
T12076LML218；化合物 ML218ML218
ML218 is an orally active, selective, potent, and blood-brain barrier-crossing inhibitor of T-type Ca2+ channels (Cav3.1, Cav3.2, Cav3.3) (IC50 for Cav3.2 and Cav3.3 is 310 nM and 270 nM, respectively).ML218 inhibits the burst activity of neurons in the subthalamic nucleus (STN).
价 格：￥电议型 号：T12076L产 地：中国大陆
-
T12076ML218 hydrochloride；化合物 T12076ML218 hydrochloride
ML218 hydrochloride is a selective and orally active T-type Ca2+ channels (Cav3.1, Cav3.2, Cav3.3) inhibitor (Cav3.2 and Cav3.3 with IC50s of 310 nM and 270 nM , respectively).
价 格：￥电议型 号：T12076产 地：中国大陆
-
T12072ML-00253764 hydrochloride；化合物 T12072ML-00253764 hydrochloride
ML-00253764 hydrochloride is an antagonist of nonpeptidic melanocortin receptor 4 (MC4R) (Ki and IC50 of 0.16 μM and 0.103 μM, respectively).
价 格：￥电议型 号：T12072产 地：中国大陆
-
T11976Mcl1-IN-4；化合物 T11976Mcl1-IN-4
Mcl1-IN-4 is an inhibitor of Mcl1 ( IC50:0.2 μM).
价 格：￥电议型 号：T11976产 地：中国大陆
-
T11876LpxH-IN-AZ1；LpxH抑制剂AZ1LpxH-IN-AZ1
LpxH-IN-AZ1 is a potent inhibitor of the UDP-2,3-diacylglucosamine pyrophosphate hydrolase, LpxH, and sulfonylpiperazine compounds.LpxH-IN-AZ1 exhibits antimicrobial activity and inhibits Klebsiella pneumoniae with an IC50 of 0.36 μM.
价 格：￥电议型 号：T11876产 地：中国大陆
-
T11824LLLanraplenib；化合物LanraplenibGS-9876；GS-9876
Lanraplenib (GS-9876) is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treatment of inflammatory diseases. Lanraplenib inhibits SYK activity in platelets via the glycoprotein VI (GPVI) receptor without prolonging bleeding time (BT) in monkeys or humans.
价 格：￥电议型 号：T11824LL产 地：中国大陆
-
T11824LLanraplenib monosuccinate；化合物 T11824LGS-9876 monosuccinate；GS-9876 monosuccinate
Lanraplenib monosuccinate inhibits SYK activity in platelets via the glycoprotein VI (GPVI) receptor without prolonging bleeding time (BT) in monkeys or humans. Lanraplenib monosuccinate is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treatment of inflammatory diseases.
价 格：￥电议型 号：T11824L产 地：中国大陆
-
T11824Lanraplenib succinate化合物 T11824GS-9876 succinate
Lanraplenib succinate inhibits SYK activity in platelets via the glycoprotein VI (GPVI) receptor without prolonging bleeding time (BT) in monkeys or humans. Lanraplenib succinate is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treatment of inflammatory diseases.
价 格：￥电议型 号：T11824产 地：中国大陆
-
T11776KRas G12C inhibitor 1；化合物 T11776KRas G12C inhibitor 1
KRas G12C inhibitor 1 is a compound that inhibits KRas G12C.
价 格：￥电议型 号：T11776产 地：中国大陆
