Name | Description | Size | Catalog # | Supplier | |
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Icilin | Icilin is a synthetic CMR1 / TRPM8 super agonist in CMR1-expressing HEK 29… | 50mg | B0084-113190 |
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Icofungipen | Icofungipen, a cyclic β-amino acid, is the representative of a novel… | n/a | 198022-65-0 |
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Icopezil maleate | The maleate salt form of Icopezil, a benzoxazol derivative, has been found… | n/a | 145815-98-1 |
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Icotinib | Icotinib Hydrochloride (BPI-2009H), or Icotinib, is a highly selective, fi… | 300mg | B0084-459334 |
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Icotinib hydrochloride | Icotinib Hydrochloride is a quinazoline-based inhibitor of epidermal growt… | 300mg | B0084-457542 |
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iCRT 14 | iCRT 14 is a novel potent inhibitor of β-catenin-responsive transcrip… | 25mg | B0084-272145 |
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iCRT5 | iCRT5 is a Potent and cell-permeable β-catenin-responsive transcripti… | n/a | 18623-44-4 |
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Idarubicin Hydrochloride | Idarubicin HCl is a hydrochloride salt form of Idarubicin which is an anth… | n/a | B0084-094874 |
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Idasanutlin | Idasanutlin; also known as RG7388 and RO5503781, is a highly potent and se… | 200mg | B0084-462568 |
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Idazoxan hydrochloride | Idazoxan hydrochloride is the hydrochloride salt of idazoxan, which is an… | n/a | 79944-56-2 |
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Idebenone | Idebenone is a synthetic analog of coenzyme Q10 (CoQ10) and a brain stimul… | 10g | B0084-094929 |
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Idelalisib | Idelalisib is a kinase inhibitor. In combination with rituximab, it was us… | 250mg | B0084-307712 |
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IDF-11774 | IDF-11774 is a hypoxia-inducible factor-1 (HIF-1) inhibitor. Study showed… | n/a | 1429054-28-3 |
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IDFP | IDFP is an organophosphorus compound that acts as an irreversible inhibito… | n/a | 615250-02-7 |
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IDH305 | IDH305 is a potent, selective and brain penetrant inhibitor of mutant isoc… | n/a | 1628805-46-8 |
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IDN-1965 | IDN-1965 is a potent, broad-spectrum, irreversible caspase inhibitor. IDN-… | n/a | 204919-14-2 |
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IDO-IN-1 | An IDO inhibitor with IC50 of 59 nM, shows activity in Hela cell (IC50=12… | n/a | 914638-30-5 |
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IDO-IN-2 | IDO-IN-2 is a potent inhibitor of IDO (indoleamine-(2,3)-dioxygenase) with… | n/a | 1668565-74-9 |
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IDO-IN-4 | A potent IDO1 inhibitor with IC50 of 8 nM in human IDO1 / HEK293 cells. Pu… | n/a | 1629125-65-0 |
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IDO-IN-5 | A potent human IDO inhibitor with IC50 of 1-10 µM. Purity >98%. MW:… | n/a | 1402837-79-9 |
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IDO-IN-6 | A potent human IDO inhibitor with IC50 of ?1 µM. Purity >98%. MW: 31… | n/a | 1402837-76-6 |
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IDO-IN-7 | A potent human IDO inhibitor with IC50 of ?1 µM. Purity >98%. MW: 31… | n/a | 1402837-78-8 |
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IDO-IN-8 | A potent human IDO inhibitor with IC50 of 1-10 µM. Purity >98%. MW:… | n/a | 1402837-77-7 |
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IDO inhibitor 1 | Purity >98%. MW: 438.23. Molecular Formula: C11H13BrFN7O4S | n/a | 1204669-37-3 |
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Idoxifene | MW: 523.458. Molecular Formula: C28H30INO | n/a | 116057-75-1 |
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Idoxuridine | 5-Iodo-2?-deoxyuridine is a nucleoside analog that can be incorporated int… | n/a | 54-42-2 |
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IDP | Purity ≥95% by HPLC. MW: 428.18 (free acid). Molecular Formula: C10H14N… | n/a | 5570 |
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IDP | Purity ≥95% by HPLC. MW: 428.18 (free acid). Molecular Formula: C10H14N… | n/a | 5570 |
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IDRA-21 | IDRA-21, an analog of cyclothiazide, inhibits AMPA receptor desensitizatio… | n/a | 22503-72-6 |
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IDX899 | IDX899 is a novel next-generation nonnucleoside reverse transcriptase inhi… | n/a | 1097733-15-7 |
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IEM 1460 | IEM 1460, an adamantane derivative, is a selective and voltage-dependent o… | n/a | 121034-89-7 |
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IEM 1754 dihydrobromide | IEM 1754 causes use- and voltage-dependent block of open channels of recom… | n/a | 162831-31-4 |
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IEM 1925 dihydrobromide | IEM 1925 dihydrobromide is the dihydrobromide salt of IEM 1925, which is a… | n/a | 258282-23-4 |
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Ifenprodil | Ifenprodil is an NMDA receptor antagonist and acts at the polyamine site.… | n/a | 23210-56-2 |
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Ifenprodil Tartrate | Ifenprodil is an atypical noncompetitive antagonist at the NMDA receptor,… | n/a | 23210-58-4 |
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Ifetroban | Ifetroban is a selective Prostaglandin receptor and Thromboxane A2 recepto… | n/a | 143443-90-7 |
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IFN alpha-IFNAR-IN-1 | IFN alpha-IFNAR-IN-1 is a nonpeptidic, low-molecular-weight inhibitor. It… | n/a | 844882-93-5 |
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Ifosfamide | Ifosfamide is a nitrogen mustard alkylating agent used in the treatment of… | n/a | 3778-73-2 |
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IG-105 | IG-105 is a potent microtubule inhibitor with potential anticancer activit… | n/a | 905978-63-4 |
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IGF-1 LR3 | IGF-1 LR3 is a lengthened analogue of human insulin-like growth factor 1 (… | n/a | BAT-006251 |
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(+)-Igmesine hydrochloride | Igmesine is a selective σ1 receptor ligand (KD = 19.1 nM), with near… | n/a | 130152-35-1 |
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Iguratimod | Iguratimod(T-614) is a selective inhibitor of cyclo-oxygenase-2 (COX-2), a… | 250mg | B0084-056331 |
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IHR 1 | IHR 1 is a potent and cell-membrane-impermeable Smo antagonist with IC50 v… | n/a | 548779-60-8 |
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II-B08 | Purity 98%. MW: 557.61. Molecular Formula: C33H27N5O4 | n/a | 1143579-78-5 |
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IITZ-01 | IITZ-01 is a potent autophagy inhibitor that is accumulated in lysosomes.… | n/a | 1807988-47-1 |
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Ikarisoside F | Ikarisoside F, a flavonol glycoside from Vancouveria hexandra, could bind… | n/a | 113558-14-8 |
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iKIX1 | iKIX1 is an inhibitor of Pdr1-dependent gene activation. It re-sensitizes… | n/a | 656222-54-7 |
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IKK 16 | IKK16 is a selective IκB kinase (IKK) inhibitor for IKK-2( IC50=40 n… | n/a | 873225-46-8 |
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IKKε-IN-1 | IKKε-IN-1 is a potent IKKε inhibitor; inhibit the in-situ… | n/a | 1292310-49-6 |
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IKK-16 HCl | IKK-16 is a potent and slective inhibitor of IκB kinase (IKK) (IC50… | n/a | 1186195-62-9 |
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