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T1557Acetylspiramycin；乙酰螺旋霉素Spiramycin II|||Foromacidin B|||ASPM|||Spiramycin B；Spiramycin II|||Foromacid
Acetylspiramycin (Spiramycin B) targets 50S ribosome to inhibit protein synthesis.
价 格：￥电议型 号：T1557产 地：中国大陆
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T15135LDirect Black 38 free acid；化合物 T15135LNSC8679|||Ferristatin II；NSC8679|||Ferristatin II
Ferristatin II (Direct Black 38 free acid) is a polysulphonated dye and promotes the degradation of transferrin receptor-1 in vitro and in vivo.
价 格：￥电议型 号：T15135L产 地：中国大陆
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T15129DiI；化合物DiIDiIC18(3)；DiIC18(3)
DiI (DiIC18(3)) is a lipophilic membrane dye. It diffuses laterally to stain the entire cell. DiI is excited to emit orange-red fluorescence which is weak in water but strong and photostable when incorporated into membranes.
价 格：￥电议型 号：T15129产 地：中国大陆
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T14914Cdk1/2 Inhibitor III；Cdk1/2 抑制剂IIICdk1/2 Inhibitor III
Cdk1/2 Inhibitor III is a selective Cdk1/2 inhibitor with an IC50 value of 2.1 μM against CDK1/cyclin B.
价 格：￥电议型 号：T14914产 地：中国大陆
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T14860CaMKII-IN-1；化合物CaMKII-IN-1CaMKII-IN-1
CaMKII-IN-1 is a potent and highly selective inhibitor of CaMKII (IC50 = 63 nM). CaMKII-IN-1 exhibited more than 100-fold higher selectivity for CaMKII over CaMKIV, MLCK, p38a, Akt1, and PKC.
价 格：￥电议型 号：T14860产 地：中国大陆
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T14572BIIE-0246；化合物 T14572AR-H 053591；AR-H 053591
BIIE-0246 is a potent and highly selective non-peptide neuropeptide Y (NPY) Y2 receptor antagonist. With an IC50 of 15 nM.
价 格：￥电议型 号：T14572产 地：中国大陆
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T14322ARP-100；化合物ARP-100MMP-2 Inhibitor III；MMP-2 Inhibitor III
ARP-100 (MMP-2 Inhibitor III) is a potent and selective matrix metalloproteinase MMP-2 inhibitor (IC50=12 nM). ARP-100 interacts with the S1´ pocket of MMP-2 and exhibits anti-invasive properties in an in vitro invasion Matrigel model. ARP-100 has low inhibitory activity against MMP-1 (>50 μM), MMP-3 (4.5 μM), MMP-7 (>50 μM) and MMP-9 (0.2 μM)[1][2].
价 格：￥电议型 号：T14322产 地：中国大陆
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T14210Amelubant；化合物 T14210BIIL 284；BIIL 284
Amelubant (BIIL 284) is a prodrug of active metabolites BIIL 260 and BIIL 315. Anti-inflammatory activity[1]. Amelubant (BIIL 284) is a potent, oral and long acting LTB4 receptor antagonist, negligibly binds to LTB4 receptor, with Kis of 221 nM and 230 nM in vital cells and membranes.
价 格：￥电议型 号：T14210产 地：中国大陆
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T1408Capecitabine；卡培他滨Xeloda|||Capecitibine|||Capiibine|||RO 09-1978；Xeloda|||卡培他滨|||Capecitibine|||Capii
Capecitabine (Capecitibine) is a fluoropyrimidine carbamate belonging to the class of antineoplastic agents called antimetabolites. As a prodrug, capecitabine is selectively activated by tumor cells to its cytotoxic moiety, 5-fluorouracil (5-FU); subsequently, 5-FU is metabolized to two active metabolites, 5-fluoro-2-deoxyuridine monophosphate (FdUMP) and 5-fluorouridine triphosphate (FUTP) by both tumor cells and normal cells. FdUMP inhibits DNA synthesis and cell division by reducing normal th
价 格：￥电议型 号：T1408产 地：中国大陆
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T13897Soyasaponin III；大豆皂苷 IIISoyasaponin III
Soyasaponin III is one of the main potentially bioactive saponins found in soy (Glycine max) and related products,and can induce apoptosis in Hep-G2 cells.
价 格：￥电议型 号：T13897产 地：中国大陆
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T13838PROTAC CRABP-II Degrader-3；化合物 T13838PROTAC CRABP-II Degrader-3
PROTAC CRABP-II Degrader-3 is a potent degrader of cellular retinoic acid binding protein (CRABP-II) based on cIAp1.
价 格：￥电议型 号：T13838产 地：中国大陆
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T13837PROTAC CRABP-II Degrader-2；化合物 T13837PROTAC CRABP-II Degrader-2
PROTAC CRABP-II Degrader-2 is a potent degrader of cellular retinoic acid binding protein (CRABP-II) based on cIAp1.
价 格：￥电议型 号：T13837产 地：中国大陆
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T13836PROTAC CRABP-II Degrader-1；化合物 T13836PROTAC CRABP-II Degrader-1
PROTAC CRABP-II Degrader-1 is a potent degrader of cellular retinoic acid binding protein (CRABP-II) based on cIAp1.
价 格：￥电议型 号：T13836产 地：中国大陆
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T1383Bitoscanate；对苯二异硫氰酸酯p-Phenylene diisothiocyanate|||Biscomate|||PDITC|||1,4-Diisothiocyanatobenzene；p
Bitoscanate (PDITC) is used in the treatment of hookworms.
价 格：￥电议型 号：T1383产 地：中国大陆
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T13776Mogroside II-?A；罗汉果皂苷 II-?AMogroside II-?A
Mogroside II-?A is isolated from Siraitia grosvenorii.
价 格：￥电议型 号：T13776产 地：中国大陆
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T13753(±)-Licarin A；化合物 T13753(±)-trans-Dehydrodiisoeugenol；(±)-trans-Dehydrodiisoeugenol
(±)-Licarin A ((±)-trans-Dehydrodiisoeugenol) is a dihydrobenzofuran neolignan, the resultant of an oxidative coupling reaction of isoeugenol and horseradish peroxidase (HRP) enzyme. (±)-Licarin A shows 100% parasites mortality at 200 μM.
价 格：￥电议型 号：T13753产 地：中国大陆
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T13740Isotanshinone IIA；化合物 T13740Isotanshinone IIA
Isotanshinone IIA, could non-competitively inhibit Protein Tyrosine Phosphatase 1B (PTP1B) activity with an IC50 0f 11.4 μM. is an abietane-type diterpene metabolite.
价 格：￥电议型 号：T13740产 地：中国大陆
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T134923,5-Diiodothyropropionic acid；3,5-二碘甲腺丙酸C082182|||Ditpa cpd；C082182|||Ditpa cpd|||3,5-二碘甲腺丙酸
3,5-Diiodothyropropionic acid (C082182) is a thyroid hormone analog. It induces α-myosin heavy chain mRNA expression, binds to thyroid hormone receptor (Ka: 2.40/M and 4.06/M for TRα1 and TRβ1).
价 格：￥电议型 号：T13492产 地：中国大陆
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T13480L(S)-(-)-5-Fluorowillardiine hydrochloride；化合物 T13480L(S)-5-Fluorowillardiine hydrochloride|||(5S)-Fl
(S)-(-)-5-Fluorowillardiine hydrochloride is a potent and specific agonist of AMPAR.
价 格：￥电议型 号：T13480L产 地：中国大陆
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T13480(S)-(-)-5-Fluorowillardiine；5-氟代尿嘧啶丙氨酸(S)-5-Fluorowillardiine|||(5S)-Fluorowillardiine；(S)-5-Fluorow
(S)-(-)-5-Fluorowillardiine ((S)-5-Fluorowillardiine) is an AMPA receptor-specific agonist
价 格：￥电议型 号：T13480产 地：中国大陆
