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T11415Glucagon receptor antagonists-3Glucagon receptor antagonists-3
Glucagon receptor antagonist -3 is a highly effective glucagon receptor antagonist.
价 格：￥电议型 号：T11415产 地：美洲
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T11434GlyRS-IN-1GlyRS-IN-1
?GlyRS-IN-1 can inhibit the growth of bacteria. is a glycyl-tRNA synthase (GlyRS) inhibitor .
价 格：￥电议型 号：T11434产 地：美洲
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T11465GS-6207GS-6207
GS-6207 displays a mean EC50 of 50 pM (20-160 pM) against 23 HIV-1 clinical isolates from different subtypes in peripheral blood mononuclear cells (PBMCs). GS-6207 is a HIV-1 capsid inhibitor. GS-6207 shows anti-HIV activity with an EC50 of 100 pM in MT-4
价 格：￥电议型 号：T11465产 地：美洲
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T1159LeflunomideLeflunomide,RS-34821,SU101
Leflunomide is an immunomodulatory agent used in the therapy of rheumatoid arthritis and psoriatic arthritis.
价 格：￥电议型 号：T1159产 地：美洲
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T11626IACS-8968IACS-8968,IDO/TDO Inhibitor,
IACS-8968 ?is a dual IDO and TDO inhibitor, with pIC50s of 6.43 for IDO and <5 for TDO, respectively.?
价 格：￥电议型 号：T11626产 地：美洲
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T11627IACS-8968 R-entiomerIACS-8968 R-entiomer,IACS-8968 R-enantiomer,IDO/TDO Inhibitor (R-enantiomer)
IACS-8968 is a dual IDO and TDO inhibitor, with pIC50s of 6.43 for IDO and <5 for TDO, respectively.?IACS-8968 ?is the R-enantiomer of IACS-8968.
价 格：￥电议型 号：T11627产 地：美洲
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T11628IACS-8968 S-entiomerIACS-8968 S-entiomer,IACS-8968 S-enantiomer,IDO/TDO Inhibitor (S-enantiomer)
IACS-8968 is a dual IDO and TDO inhibitor, with pIC50s of 6.43 for IDO and <5 for TDO, respectively.?IACS-8968 ?is the S-enantiomer of IACS-8968.
价 格：￥电议型 号：T11628产 地：美洲
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T11740DelcasertibDelcasertib,KAI-9803,BMS-875944
Delcasertib is a potent and selective δ-protein kinase C (δPKC) inhibitor.
价 格：￥电议型 号：T11740产 地：美洲
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T11824Lanraplenib succinateLanraplenib succinate,GS-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 devel
价 格：￥电议型 号：T11824产 地：美洲
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T11824LLLanraplenibLanraplenib,GS-9876,
Lanraplenib inhibits SYK activity in platelets via the glycoprotein VI (GPVI) receptor without prolonging bleeding time (BT) in monkeys or humans. Lanraplenib is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treat
价 格：￥电议型 号：T11824LL产 地：美洲
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T1183RetinolRetinol,all-trans-Retinol,Vitamin A1
Retinol and derivatives of retinol that play an essential role in metabolic functioning of the retina, the growth of and differentiation of epithelial tissue, the growth of bone, reproduction, and the immune response. Dietary vitamin A is derived from a v
价 格：￥电议型 号：T1183产 地：美洲
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T11832Ledipasvir D-tartrateLedipasvir D-tartrate,GS-5885 D-tartrate,
Ledipasvir D-tartrate with EC50 values of 34 pM against GT1a and 4 pM against GT1b replicon.?is an inhibitor of the hepatitis C virus NS5A.
价 格：￥电议型 号：T11832产 地：美洲
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T11902LY 344864 S-entiomerLY 344864 S-entiomer,LY 344864 S-enantiomer,
LY 344864 S-enantiomer is the S-enantiomer of LY344864. LY344864 is a 5-HT1F receptor agonist.?
价 格：￥电议型 号：T11902产 地：美洲
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T11917Lys-SMCC-DM1Lys-SMCC-DM1,Lys-Nε-MCC-DM1,
DM1 is a tubulin inhibitor.?Lys-SMCC-DM1 is the active metabolite of DM1.?
价 格：￥电议型 号：T11917产 地：美洲
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T11920LysRs-IN-2LysRs-IN-2
LysRs-IN-2 is a lysyl-tRNA synthetase (KRS) inhibitor with IC50s of 0.13 μM and 0.015 μM for Cryptosporidium parvum lysyl-tRNA synthetase (CpKRS)?and Plasmodium falciparum lysyl-tRNA synthetase (PfKRS), respectively.
价 格：￥电议型 号：T11920产 地：美洲
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T12040MilademetanMilademetan,DS-3032,
Milademetan is a specific and oral inhibitor of MDM2.
价 格：￥电议型 号：T12040产 地：美洲
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T12143N-deacetylated BMS-202N-deacetylated BMS-202
N-deacetylated BMS-202 is the deacetylated of BMS-202.
价 格：￥电议型 号：T12143产 地：美洲
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T12236NMS-859NMS-859
NMS-859 is a potent and covalent inhibitor of VCP (p97)(IC50s of 0.37 and 0.36 μM for wild-type VCP in the presence of 60 μM and 1 mM ATP in cells, respectively).
价 格：￥电议型 号：T12236产 地：美洲
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T12237NMS-P715NMS-P715
NMS-P715 is a selective and ATP-competitive MPS1 inhibitor(IC50 of 182 nM).
价 格：￥电议型 号：T12237产 地：美洲
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T12254NS-3-008 hydrochlorideNS-3-008 hydrochloride
NS-3-008 hydrochloride is an orally active transcriptional G0/G1 switch 2 (G0s2) inhibitor (IC50 of 2.25 μM).
价 格：￥电议型 号：T12254产 地：美洲
