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TN119517-Hydroxy sprengerinin CPolygonatum sibiricum,17Hydroxy sprengerinin C,17-Hydroxy sprengerinin C,pr
17-Hydroxy sprengerinin C is a glycoside compound isolated from rhizomes of Polygonatum sibiricum with stronger anticancer activities. 17-Hydroxy sprengerinin C reduces the expression of Blc-2 and pro-caspase3 and increases the production of Bax.
价 格：￥电议型 号：TN1195产 地：中国大陆
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T9580SB-734117SB 734117,SB734117
SB-734117 inhibits productive replication of several HCMV strains. SB-734117 exhibited polypharmacology and was an inhibitor of several proteins from the AGC and CMCG kinase groups.
价 格：￥电议型 号：T9580产 地：中国大陆
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T9585GNE-9815
GNE-9815 is a high kinase-selective inhibitor of RAF and targets KRAS-mutant cancers through combination therapy.
价 格：￥电议型 号：T9585产 地：中国大陆
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T9578ELOVL1-IN-1chain,inhibit,adrenoleukodystrophy,Inhibitor,ELOVL1IN1,ALD,fatty,ELOVL-1-IN-1,acid,ELOVL1
ELOVL1-IN-1 is an ELOVL1 inhibitor. ELOVL1-IN-1 can reduce the levels of very long chain fatty acids. ELOVL1-IN-1 can be used in the study of adrenoleukodystrophy (ALD).
价 格：￥电议型 号：T9578产 地：中国大陆
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T7954YM976YM-976,Phosphodiesterase (PDE),PDE4 inhibitor,inhibit,phosphodiesterase 4,anti-inflammatory act
YM976 is an orally active PDE4 inhibitor (IC50:2.2 nM)
价 格：￥电议型 号：T7954产 地：中国大陆
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T7940Milnacipran ((1S-cis) hydrochloride)SERT,Milnacipran ((1S-cis) hydrochloride),F-2695,Milnacipran ((1
Milnacipran ((1S-cis) hydrochloride) is a serotonin-norepinephrine reuptake inhibitor (SNRI), treatment of fibromyalgia.
价 格：￥电议型 号：T7940产 地：中国大陆
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T9579LGLP-1 receptor agonist 9 citrate
GLP-1 receptor agonist 9 citrate is an agonist of GLP-1.
价 格：￥电议型 号：T9579L产 地：中国大陆
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T36395Trotabresib
CC-90010 is an orally active inhibitor of BET and can be used in studies about advanced solid tumors.
价 格：￥电议型 号：T36395产 地：中国大陆
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T9956VK-28VK28,VK 28
VK-28 is a brain permeable iron chelator with neuroprotection. VK-28 inhibits basal as well as iron-induced mitochondrial lipid peroxidation.
价 格：￥电议型 号：T9956产 地：中国大陆
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T7318Elimusertibresponse,damage,ATM/ATR,stress,Inhibitor,BAY1895344,tumors,DNA,instability,lymphomas,inhi
BAY 1895344 is a potent, highly selective and orally available ATR inhibitor with an IC50 of 7 nM.BAY 1895344 shows potent anti-tumor efficacy in monotherapy and strong combination potential with the targeted alpha therapy Radium-223 dichloride.
价 格：￥电议型 号：T7318产 地：中国大陆
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T7956(+)-Fenchoneinhibit,(+)Fenchone,(+) Fenchone,Inhibitor,(+)-Fenchone
(+)-Fenchone has anti-inflammatory and antimicrobial activities
价 格：￥电议型 号：T7956产 地：中国大陆
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TQ0091LY2795050LY2795050,Inhibitor,central nervous system dysfunction,sex differences,inhibit,Opioid Recep
LY2795050 is a novel specific κ-Opioid Receptor antagonist (IC50: 0.72 nM).
价 格：￥电议型 号：TQ0091产 地：中国大陆
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T7495Hexa-D-arginineinhibit,furin,Furin Inhibitor II,TNF-α,PACE4,noncytotoxic,PC1,anthrax,PEA,HexaDargini
Hexa-D-arginine is an inhibitor of furin,blocks the activation of Pseudomonas aeruginosa exotoxin A in vivo.
价 格：￥电议型 号：T7495产 地：中国大陆
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TN71951,8-Diazabicyclo[5.4.0]undec-7-ene
1,8-Diazabicyclo[5.4.0]undec-7-ene is a marine derived natural products found in Niphates digitalis.
价 格：￥电议型 号：TN7195产 地：中国大陆
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T60065WAY-118959-AWAY 118959 A,WAY118959A
WAY-118959-A is a potential microtubule acetylation inhibitor.
价 格：￥电议型 号：T60065产 地：中国大陆
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T8495AlobresibInhibitor,GS5829,Alobresib,GS 5829,Epigenetic Reader Domain,inhibit
Alobresib is an inhibitor of BET bromodomain,is an antineoplastic drug candidate.
价 格：￥电议型 号：T8495产 地：中国大陆
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TP1095ElamipretideElamipretide
Elamipretide (SS-31,MTP-131,Bendavia) is a small mitochondrially-targeted tetrapeptide (D-Arg-dimethylTyr-Lys-Phe-NH2) that appears to reduce the production of toxic reactive oxygen species and stabilize cardiolipin.
价 格：￥电议型 号：TP1095产 地：中国大陆
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TN1950Moracin MMoracin M
Moracin M, a phenolic component in the skin of Morus alba Linn., is a potent phosphodiesterase-4 (PDE4) inhibitor with IC50 values of 2.9, 4.5, >40, and >100 μM for PDE4D2, PDE4B2, PDE5A1, and PDE9A2, respectively. Moracin M has anti-inflammatory activity.
价 格：￥电议型 号：TN1950产 地：中国大陆
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T23316SB 218795constriction,SB-218795,Neurokinin Receptor,Inhibitor,neurokinin-3,NK receptor,pupillary,inh
SB 218795 is an effective and selective antagonist of NK3 with a Ki 13 nM for hNK3 which is about 90-fold and 7000-fold selectivity over hNK2 and hNK1.
价 格：￥电议型 号：T23316产 地：中国大陆
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T9592OATD-01inhibit,CHIT1,OATD-01,chitinase,antifibrotic,IPF,pulmonary fibrosis,OATD01,OATD 01,Inhibitor
OATD-01 is a highly active inhibitor of both Chitotriosidase (CHIT1) and acidic mammalian chitinase (AMCase).
价 格：￥电议型 号：T9592产 地：中国大陆
