Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
6111505 | Itacitinib | 1334298-90-6 | 98% | |
Itacitinib (INCB039110) is an oral selective JAK1 inhibitor. Itacitinib is an inh | ||||
611914 | IC261 | 186611-52-9 | 98% | |
IC261 is a novel inhibitor of CK1, triggers the mitotic checkpoint control. The IC50 | ||||
611811 | Imeglimin | 775351-65-0 | 98% | |
Imeglimin(EMD-387008) is the first in a new tetrahydrotriazine-containing class of or | ||||
160926004 | IC-87114 | 371242-69-2 | 98% by HPLC | |
It Inhibits p110, p110 and p110 only at much higher concentrations. It does not inhib | ||||
16071103 | Iniparib | 160003-66-7 | 98% by HPLC | |
Iniparib, also known as BSI-201, is a small-molecule prodrug inhibitor of the nuclear | ||||
16070812 | Idasanutlin (RG7388) | 1229705-06-9 | 98% by HPLC | |
Idasanutlin; also known as RG7388 and RO5503781, is a highly potent and selective MDM | ||||
16070809 | Istradefylline | 155270-99-8 | 98% by HPLC | |
Istradefylline (KW-6002) is a selective antagonist at the A2A receptor. It has been f | ||||
16070104 | Ilomastat | 142880-36-2 | 98% by HPLC | |
Ilomastat, also known as GM6001 and galardin, is a broad-spectrum matrix metalloprote | ||||
16062116 | IRAK-1-4 Inhibitor I | 448906-42-1 | 98% by HPLC | |
IRAK-1-4 Inhibitor I | ||||
16053001 | Ivosidenib | 1448347-49-6 | 98% by HPLC | |
Ivosidenib is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1) | ||||
032405 | INCB 024360 | 1204669-58-8 | 98% | |
INCB 024360 is a potent and novel indoleamine-2,3 dioxygenase (IDO)inhibitor with an | ||||
021701 | 5-Iodo-2-isopropyl-1-methyl-1H-imidazole | 851870-28-5 | 98% | |
Coming soon! | ||||
011310 | Irbinitinib | 937263-43-9 | 98% | |
Irbinitinib is a potent and selective HER2 inhibitor with IC50 of 8 nM, equipotent ag | ||||
011121 | INK-128 | 1224844-38-5 | 98% | |
INK 128 is a potent and selective mTOR inhibitor with IC50 of 1 nM; >200-fold less | ||||
011109 | IWP L6 | 1427782-89-5 | 98% | |
IWP L6 is a Porcn inhibitor with EC50 of 0.5 nM. | ||||
011101 | Icotinib | 610798-31-7 | 98% | |
Icotinib is an orally available quinazoline-based inhibitor of epidermal growth facto | ||||
010801 | IWP-3 | 687561-60-0 | 98% | |
IWP-3 is an inhibitor of Wnt production. | ||||
010612 | Isoquinolin-7-ylboronic acid | 1092790-21-0 | 98% | |
This product is for custom synthesis. | ||||
010419 | IKK 16 | 1186195-62-9 | 98% | |
Coming soon! | ||||
123002 | IDO-IN-2 | 914471-09-3 | 98% | |
IDO-IN-2 is a potent IDO1 inhibitor(IC50=10 nM) with desirable pharmaceutical propert | ||||
122905 | INT-747 | 459789-99-2 | 98% | |
INT-747 is a potent and selective FXR agonist(EC50=99 nM) endowed with anticholestati | ||||
122801 | ICG-001 | 780757-88-2 | 98% | |
ICG-001 is a potent, specific inhibitor of the canonical Wnt signaling pathway in can | ||||
122307 | Ixabepilone | 219989-84-1 | 98% | |
Ixabepilone is an epothilone B analog and nontaxane microtubule-stabilizing compound | ||||
120801 | Isavuconazole | 241479-67-4 | 98% | |
Coming soon! | ||||
110907 | IRAK-1-4 Inhibitor I | 509093-47-4 | 98% | |
IRAK-1-4 Inhibitor I is a IRAK-4 Inhibitor with IC50 of 200 nM, and is an anti-inflam | ||||
110602 | IWP-2 | 686770-61-6 | 98% | |
IWP-2 is an inhibitor of Wnt secretion and processing. It blocks Wnt-dependent signal | ||||
102701 | Indiplon | 325715-02-4 | 98% | |
Indiplon is a pyrazolopyrimidine that acts as a high-affinity positive allosteric mod | ||||
102620 | INH6 | 1001753-24-7 | 98% | |
INH6 is a potent Hec1 inhibitor, which specifically disrupts the Hec1/Nek2 interactio | ||||
102606 | INH1 | 313553-47-8 | 98% | |
INH1 is a small molecule targeting the Hec1/Nek2 mitotic pathway suppresses tumor cel | ||||
101902 | ITD-1 | 1099644-42-4 | 98% | |
ITD-1 is a selective inhibitor of TGF- signaling, displays little or no inhibition of |
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