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T19670BMS-538203；化合物 T19670BMS-538203
BMS-538203 is a novel HIV integrase inhibitor.
价 格：￥电议型 号：T19670产 地：中国大陆
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T19633Ionox 330；抗氧剂 330Antioxidant 40|||BRN 2034522|||Ahydol|||Antioxidant 330|||AO-40；Antioxidant 40|||BR
Ionox 330 (Ahydol) is an alkylphenol compound used as an antioxidant.
价 格：￥电议型 号：T19633产 地：中国大陆
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T19203Bendamustine D4；化合物 T19203SDX-105 D4；SDX-105 D4
Bendamustine D4 is the deuterium-labeled Bendamustine. Bendamustine is a DNA cross-linking compound with alkylating and antimetabolite properties. Bendamustine causes DNA breaks.
价 格：￥电议型 号：T19203产 地：中国大陆
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T191203-Hydroxydodecanoic acid；化合物 T191203-Hydroxydodecanoic acid
3-Hydroxydodecanoic acid is a medium-chain fatty acid commonly linked to fatty acid metabolic disorders.
价 格：￥电议型 号：T19120产 地：中国大陆
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T18203m-PEG48-amine；化合物 T18203m-PEG48-amine
m-PEG48-amine is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T18203产 地：中国大陆
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T1764Adezmapimod；化合物SB203580PB 203580|||RWJ 64809|||SB203580；PB 203580|||4-(4-氟苯基)-2-(4-甲基亚磺酰基苯基)-5-(4-吡啶
Adezmapimod (SB 203580) is a p38 MAPK inhibitor (IC50=0.3-0.5 μM) that is selective and ATP-competitive. Adezmapimod possesses autophagy and mitochondrial autophagy activating activity. Adezmapimod displays more than 100-fold higher selectivity than PKB, LCK, and GSK-3β.
价 格：￥电议型 号：T1764产 地：中国大陆
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T17203UNC0224；化合物UNC0224UNC0224
UNC0224 is a selective inhibitor of G9a with a Ki of 2.6 nM and IC50 of 15 nM. UNC0224 also potently inhibits GLP with assay-dependent IC50 values of 20-58 nM.
价 格：￥电议型 号：T17203产 地：中国大陆
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T1687LDoxycycline (hyclate)盐酸强力霉素Doxycycline hydrochloride hemiethanolate hemihydrate|||盐酸强力霉素|||WC2031|||
Doxycycline hyclate (WC2031) belongs to the tetracycline class of antibiotics and is a broad-spectrum metalloproteinase (MMP) inhibitor with oral activity. Doxycycline hyclate has antibacterial activity and antitumor activity.
价 格：￥电议型 号：T1687L产 地：中国大陆
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T16720Rafigrelide；化合物 T167203,3-Dimethylanagrelide；3,3-Dimethylanagrelide
Rafigrelide is a platelet-lowering agent.
价 格：￥电议型 号：T16720产 地：中国大陆
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T1669LLiothyronine HCl；化合物 T1669LTriiodothyronine|||L-T3|||NSC 80203|||Liothyronine|||Liotironina|||L-Liot
Liothyronine is a T3 thyroid hormone normally synthesized and secreted by the thyroid gland in much smaller quantities than thyroxine.
价 格：￥电议型 号：T1669L产 地：中国大陆
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T16573Pratosartan；化合物 T16573KT 3671|||FW 7203|||KD 3-671；KT 3671|||FW 7203|||KD 3-671
Pratosartan is a selective antagonist of angiotensin II receptor.
价 格：￥电议型 号：T16573产 地：中国大陆
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T16203N-Boc-N-bis(C2-PEG1-azide)；化合物 T16203N-Boc-N-bis(C2-PEG1-azide)
N-Boc-N-bis(C2-PEG1-azide) is an alkyl/ether-based PROTAC linker suitable for synthesizing PROTACs[1].
价 格：￥电议型 号：T16203产 地：中国大陆
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T15427GSK2033；化合物GSK2033GSK2033
GSK2033 is an antagonist of LXR (pIC50s: 7 and 7.4 for LXRα or LXRβ, respectively).
价 格：￥电议型 号：T15427产 地：中国大陆
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T15270Fananserin；法南色林RP 62203；RP 62203|||法南色林
Fananserin is an effective, selective and oral active antagonist of 5-HT2 (Ki = 0.37 nM for the rat 5-HT2A). Fananserin is an antagonist of human D4 receptor (Ki = 2.93 nM).
价 格：￥电议型 号：T15270产 地：中国大陆
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T15203EGNHS；化合物EGNHSEGS crosslinker；EGS crosslinker
EGNHS (EGS crosslinker) is an alkyl/ether-based PROTAC linker that can be used in the synthesis of PROTACs[1].
价 格：￥电议型 号：T15203产 地：中国大陆
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T15170DS28120313；化合物 T15170DS28120313
DS28120313 is an oral inhibitor of hepcidin production (IC50: 0.093 μM).
价 格：￥电议型 号：T15170产 地：中国大陆
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T1492Gemifloxacin mesylate；甲磺酸吉米沙星LB-20304a|||SB-265805S|||Gemifloxacinu00A0mesylate；LB-20304a|||甲磺酸吉米沙星|
Gemifloxacin mesylate (Gemifloxacin?mesylate) inhibits activities of DNA gyrase and topoisomerase IV, thereby inhibiting DNA replication and eventually bacterial growth. Gemifloxacin Mesylate is the mesylate salt form of gemifloxacin, a synthetic broad-spectrum fluoroquinolone with antibacterial activity. This fluoroquinolone exerts an enhanced spectrum of activity against gram-positive bacteria such as Streptococcus pneumonia and Staphylococcus aureus, in addition to its activity against gram-n
价 格：￥电议型 号：T1492产 地：中国大陆
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T14902CCT020312；化合物CCT020312CCT020312
CCT020312 is a selective activator of EIF2AK3 and PERK. CCT020312 durably inhibits cell proliferation and elicits the phosphorylation of EIF2A.
价 格：￥电议型 号：T14902产 地：中国大陆
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T14203AM-8735；化合物 T14203AM-8735
AM-8735 is an inhibitor of MDM2 ( IC50: 25 nM).
价 格：￥电议型 号：T14203产 地：中国大陆
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T14147Pelitrexol；化合物 T14147AG 2037；AG 2037
Pelitrexol (AG 2037) is a glycinamide ribonucleotide formyltransferase (GARFT) inhibitor.
价 格：￥电议型 号：T14147产 地：中国大陆
