9月
Tos-PEG2-CH2COOH；化合物 T17124Tos-PEG2-CH2COOH (2024/9/1)
简介：tos-peg2-ch2cooh 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.
Tos-PEG2-CH2-Boc；化合物 T17123Tos-PEG2-CH2-Boc (2024/9/1)
简介：tos-peg2-ch2-boc 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.
Tos-PEG2-C2-Boc；化合物 T17122Tos-PEG2-C2-Boc (2024/9/1)
简介：tos-peg2-c2-boc 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.
Tos-PEG1-CH2-Boc；化合物 T17121Tos-PEG1-CH2-Boc (2024/9/1)
简介：tos-peg1-ch2-boc 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.
Tos-PEG2-Boc；化合物 T17120Tos-PEG2-Boc (2024/9/1)
简介：tos-peg2-boc 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.
Tos-aminoxy-Boc-PEG4-Tos；化合物 T17119Tos-aminoxy-Boc-PEG4-Tos (2024/9/1)
简介：tos-aminoxy-boc-peg4-tos is a peg4-based protac linker utilized for the synthesis of protacs[1].
Tonapofylline；化合物TonapofyllineBG 9928；BG 9928 (2024/9/1)
简介：tonapofylline is an orally active and selective antagonist of the a1 adenosine receptor (ki: 7.4 nm for human a1). tonapofylline can be used in studies about heart failure.
Tonabersat；化合物 T17116SB-220453；SB-220453 (2024/9/1)
简介：tonabersat is a modulator of the gap-junction.
Tolycaine；托利卡因Tolycaine (2024/9/1)
简介：tolycaine is a compound of local anesthetic.
Tolrestat；托瑞司他AY-27773；托瑞司他|||AY-27773 (2024/9/1)
简介：tolrestat (ay-27773) is a potent inhibitor of aldose reductase (ic50 = 35 nm).
Tolonidine；化合物 T17113Tolonidine (2024/9/1)
简介：tolonidine is orally active and has been shown to possess hypotensive. tolonidine is a derivative of imidazoline.
Todralazine；化合物 T17112Ecarazine；Ecarazine (2024/9/1)
简介：todralazine is an anti-hypertensive agent and acts as a β2ar blocker. it also has an antioxidant and free radical scavenging activity.
Todralazine hydrochloride；盐酸托屈嗪Ecarazine hydrochloride；Ecarazine hydrochloride|||盐酸托屈嗪 (2024/9/1)
简介：todralazine hydrochloride (ecarazine hydrochloride) is a β2ar blocker and has antioxidant and free radical scavenging activities. todralazine hydrochloride can be used in anti-hypertensive research.
TNP-470；化合物 T17110AGM-1470；AGM-1470 (2024/9/1)
简介：tnp-470 is a methionine aminopeptidase-2 inhibitor. tnp-470 is also an angiogenesis inhibitor.
TMRM；四甲基罗丹明甲酯TMRM (2024/9/1)
简介：tmrm is a cell-permeant cationic lipophilic red fluorescent dye (λex: 530 nm, λem: 592 nm).
TMRM Perchlorate四甲基若丹明甲酯酸铵四甲基若丹明甲酯酸铵|||T668 (2024/9/1)
简介：tmrm perchlorate (t668) is a cell-permeant cationic lipophilic red fluorescent dye (λex=530 nm, λem=592 nm).
TMP920；化合物 T17108TMP920 (2024/9/1)
简介：tmp920 inhibits rorγt binding to the src1 peptide (ic50: 0.03 μm). tmp920 is a highly potent and selective rorγt antagonist.
TMC353121；化合物 T17107TMC353121 (2024/9/1)
简介：tmc353121 is an effective inhibitor of respiratory syncytial virus fusion (pec50: 9.9).
TMC310911；化合物 T17106TMC310911 (2024/9/1)
简介：tmc310911 is an effective and orally active hiv type-1 protease inhibitor (ec50: ranged from 2.2 nm to 14.2 nm for wild-type hiv-1). tmc310911 has effective activity against a wide spectrum of recombinant hiv-1 isolates.
TM6089；化合物TM6089TM6089 (2024/9/1)
简介：tm6089 is an inhibitor of prolyl hydroxylase that stimulates hif activity without iron chelation, induces angiogenesis, and protects organ against ischemia.
TM-N1324；化合物TM-N1324TM-N1324 (2024/9/1)
简介：tm-n1324 is a gpr39 agonist. tm-n1324 activates human gpr39 with high efficacy and potencies of 280 nm and 9 nm in the absence and presence of zn2+, respectively. tm-n1324 has similar potencies to murine gpr39 with ec50s of 180 nm and 5 nm, respectively.
Tipifarnib (S enantiomer)；化合物Tipifarnib S entiomerTipifarnib S enantiomer|||(S)-(-)-R-115777|||(S)-T (2024/9/1)
简介：tipifarnib s enantiomer ((s)-(-)-r-115777) is the s-enantiomer of tipifarnib. tipifarnib is a potent and specific farnesyltransferase inhibitor (ic50: 0.6 nm).
Tiopinac；硫平酸RS 40974|||RS40974|||硫平酸|||RS-40974|||RS 40974|||Tiopinac|||RS 40974|||Tiopinac；RS 40974 (2024/9/1)
简介：tiopinac is a tricyclic compound with potent anti-inflammatory, analgesic and antipyretic effects in animals, the ability to inhibit prostaglandin synthesis, and moderate anti-platelet aggregation properties in humans.
Tin(IV) mesoporphyrin IX dichloride；化合物 T17100Stannsoporfin；Stannsoporfin (2024/9/1)
简介：tin(iv) mesoporphyrin ix dichloride is a heme oxygenase inhibitor being developed for the prevention of hyperbilirubinemia in infants at risk of developing jaundice.
Trolox；奎诺二甲基丙烯酸酯Trolox (2024/9/1)
简介：trolox is a derivative of vitamin e that is cell permeable and water soluble. trolox is a membrane damage inhibitor with potent antioxidant activity.
Timapiprant sodium；化合物 T17099OC000459 sodium；OC000459 sodium (2024/9/1)
简介：timapiprant sodium inhibits mast cell activation of th2 lymphocytes and eosinophils. timapiprant sodium is a potent and selective d prostanoid receptor 2 antagonist. timapiprant sodium potently displaces [3h] pgd2 from human recombinant dp2 (ki=13 nm), rat recombinant dp2 (ki=3 nm), human native dp2 (ki=4 nm).
Tilfrinib；化合物TilfrinibTilfrinib (2024/9/1)
简介：tilfrinib is an effective and selective inhibitor of breast tumor kinase(brk, ic50 = 3.15 nm) which displays anti-proliferative and anti-tumor activities.
Tilbroquinol；甲溴羟喹Tilbroquinol (2024/9/1)
简介：tilbroquinol is an antiprotozoal agent effective against amoebiasis.
Tilapertin；化合物 T17096AMG747；AMG747 (2024/9/1)
简介：tilapertin is an oral glycine transporter type-1 inhibitor.
TIK-301；化合物 T17095PD-6735|||LY-156735；PD-6735|||LY-156735 (2024/9/1)
简介：tik-301 is a chlorinated melatonin derivative and a potent, high-affinity, and orally active melatonin mt1 and mt2 receptors agonist (kis: 0.081 nm and 0.042 nm, respectively). tik-301 is also a 5-ht2b/5-ht2c receptor antagonist with antidepressant action. tik-301 has the potential for sleep disorders and other circadian rhythm disorders treatment.
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