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T16708R-268712R-268712
R-268712 is an effective and selective inhibitor of ALK5 IC50: 2.5 nM).
价 格：￥电议型 号：T16708产 地：美洲
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T16796RPR-260243RPR-260243
RPR-260243 is a novel activator of HERG and modifies HERG currents inhibited by dofetilide (IC50 = 58 nM).
价 格：￥电议型 号：T16796产 地：美洲
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T16841SAR-260301SAR-260301
SAR-260301 is an orally available and selective inhibitor of PI3Kβ (IC50: 23 nM).
价 格：￥电议型 号：T16841产 地：美洲
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T5452Ehp-inhibitor-2Ehp-inhibitor-2
Ehp-inhibitor-2 is an Eph family tyrosine kinase inhibitor targeting Eph receptors.
价 格：￥电议型 号：T5452产 地：美洲
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T5678N-(2-Aminoethyl)-5-chlor-2-pyridincarboxN-(2-Aminoethyl)-5-chlor-2-pyridincarbox,Lazabemide hydrochl
N-(2-Aminoethyl)-5-chlor-2-pyridincarbox is a reversible and selective mao-b inhibitor(Ki：7.9nM).
价 格：￥电议型 号：T5678产 地：美洲
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T6289DovitinibDovitinib,TKI258,CHIR-258
Dovitinib (TKI258, CHIR258) is a multitargeted RTK inhibitor, mostly for class III (FLT3/c-Kit, IC50: 1/2 nM), also effective to class IV (FGFR1/3) and class V (VEGFR1-4) RTKs (IC50: 8-13 nM), less potent to EGFR, InsR, EphA2, c-Met, IGF-1R, Tie2, and HER
价 格：￥电议型 号：T6289产 地：美洲
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T6301TosedostatTosedostat,CHR-2797,
CHR-2797 is an orally bioavailable inhibitor of the M1 family of aminopeptidases with potential antineoplastic activity. CHR-2797 is converted intracellularly into a poorly membrane-permeable active metabolite (CHR-79888) which inhibits the M1 family of a
价 格：￥电议型 号：T6301产 地：美洲
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T6561LaquinimodLaquinimod,ABR-215062,LAQ
Laquinimod is an effective immunomodulator, which is currently under development in phase III trials for the treatment of multiple sclerosis as an oral therapy.
价 格：￥电议型 号：T6561产 地：美洲
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T8817TIE-2/VEGFR-2 kinase-IN-1；化合物 T8817TIE-2/VEGFR-2 kinase-IN-1
TIE-2/VEGFR-2 kinase-IN-1 is used for the synthesis of TIE-2 and/or VEGFR-2 inhibitors that can be used for the study of diseases associated with inappropriate angiogenesis [1].
价 格：￥电议型 号：T8817产 地：中国大陆
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T8744PROTAC BRAF-V600E degrader-2；化合物 T8744PROTAC BRAF-V600E degrader-2
PROTAC BRAF-V600E degrader-2 is a useful organic compound for research related to life sciences. The catalog number is T8744 and the CAS number is 2417296-82-1.
价 格：￥电议型 号：T8744产 地：中国大陆
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T83699LL-37 (18-37) (human) TFA；化合物 LL-37 (18-37) (human) TFAKR-20|||hCAP-18|||CAP-18|||Cathelicidin|||FAL
LL-37 (18-37), an antimicrobial peptide fragment of LL-37, exhibits activity against S. aureus and C. albicans, with minimum lethal concentrations of 4 ?M and 10 ?M, respectively. Additionally, it inhibits E. histolytica trophozoites growth at concentrations between 10 to 50 ?M.
价 格：￥电议型 号：T83699产 地：中国大陆
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T83579(12β)-20-(β-D-Glucopyranosyloxy)-12-hydroxydammar-24-en-3-one；化合物 (12β)-20-(β-D-Glucopyranosyloxy)-1
´(12β)-20-(β-D-Glucopyranosyloxy)-12-hydroxydammar-24-en-3-one is a naturally occurring compound isolated from Cladosporium microorganisms [1].´
价 格：￥电议型 号：T83579产 地：中国大陆
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T83121Anatumomab mafenatox；化合物 Anatumomab mafenatoxABR-214936；ABR-214936
Anatumomab mafenatox (ABR-214936), a 73 KDa recombinant protein, targets the tumor-associated antigen 5T4 commonly expressed in malignancies. It is a conjugate comprising a modified form of SEA linked to a murine Fab. The primary adverse effects of Anatumomab mafenatox include fever, hypotension, pain, nausea, and drowsiness [1].
价 格：￥电议型 号：T83121产 地：中国大陆
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T82997Antitumor photosensitizer-2；化合物 Antitumor photosensitizer-2Antitumor photosensitizer-2
Compound 11, also known as Antitumor Photosensitizer-2, is a potent photosensitizer with remarkable photodynamic anti-tumor properties and minimal skin photo-toxicity, representing a promising candidate for photodynamic therapy research [1].
价 格：￥电议型 号：T82997产 地：中国大陆
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T82481Elebsiran sodium；化合物 Elebsiran sodiumVIR-2218 sodium；VIR-2218 sodium
Elebsiran sodium is an siRNA targeting hepatitis B and D virus infections [1].
价 格：￥电议型 号：T82481产 地：中国大陆
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T82253GSPT1 degrader-2；化合物 GSPT1 degrader-2GSPT1 degrader-2
GSPT1 degrader-2 is a potent degrader of GSPT1 [1].
价 格：￥电议型 号：T82253产 地：中国大陆
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T81973KR-27425；化合物 KR-27425KR-27425
Compound 13, an AChE activator 1, is a non-pyridinium oxime that reactivates paraoxon-inhibited acetylcholinesterase (AChE) [1].
价 格：￥电议型 号：T81973产 地：中国大陆
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T81483Photosensitizer-2；化合物 Photosensitizer-2Photosensitizer-2
Photosensitizer-2 (compound 1), an organic D-π-A sensitizer, exhibits antitumor properties and potent phototoxicity due to an acrylic acid moiety. It demonstrates significant activity against HeLa cells, with IC 50 values of 20.9 ± 4.5 μM (dark) and 0.046 ± 0.012 μM (irradiation) [1].
价 格：￥电议型 号：T81483产 地：中国大陆
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T81386PROTAC BRD4 Degrader-22；化合物 PROTAC BRD4 Degrader-22PROTAC BRD4 Degrader-22
PROTAC BRD4 Degrader-22 (Compd 44h) is a PROTAC-based degrader targeting BRD4, exhibiting a pDC50 of 9.2 in MOLT4 cells over 24 hours [1].
价 格：￥电议型 号：T81386产 地：中国大陆
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T81385PROTAC BRD9 Degrader-2；化合物 PROTAC BRD9 Degrader-2PROTAC BRD9 Degrader-2
PROTAC BRD9 Degrader-2 is a bifunctional compound designed for the targeted degradation of BRD9 in cancer research applications.
价 格：￥电议型 号：T81385产 地：中国大陆
