Catalog No | Chemical Name | CAS Number | Purity | Chemical Structure |
---|---|---|---|---|
184214 | OSS-128167 | 887686-02-4 | >98% | |
OSS-128167, 也称为SIRT6-IN-1, 是一种有效且具有选择性的SIRT 6 抑制剂 | ||||
1712154 | Osimertinib mesylate | 1421373-66-1 | >98% | |
Osimertinib,也被称为Mereletinib和AZD- 9291,是第三代EGFR抑制剂,为晚 | ||||
1791513 | Oxytocin acetate | 6233-83-6 | 98.0% | |
Oxytocin is a medication and hormone. As a medication, it is used to cause contractio | ||||
1791319 | ON1231320 | 131247-39-8 | 98.0% | |
ON1231320, also known as GBO-006, is a Polo-like kinase 2 (PLK2) inhibitor. | ||||
179824 | Olodaterol HCl | 869477-96-3 | 98.0% | |
Olodaterol, also known as BI 1744, is a long acting beta-adrenoceptor agonist used as | ||||
110902 | Ozanimod | 1306760-87-1 | 98% | |
Ozanimod is a selective sphingosine 1 phosphate receptor modulators and methods which | ||||
011103 | Olmutinib | 1353550-13-6 | 98% | |
Olmutinib is a potent small molecule inhibitor of Bruton's tyrosine kinase (BTK). | ||||
178308 | OXi-4503 sodium | 288847-34-7 | 98.0% | |
OXi-4503 is the diphosphate prodrug of the stilbenoid combretastatin A1, originally i | ||||
20177315 | 6-Oxaspiro[4.5]decan-9-ol | 855398-58-2 | 96.0% | |
6-Oxaspiro[4.5]decan-9-ol|15080-A1 | ||||
732801 | Olumacostat Glasaretil | 1261491-89-7 | 98% by HPLC | |
Olumacostat glasaretil is a novel topical sebum inhibitor in the treatment of acne vu | ||||
17031015 | OTS514 | 1338540-63-8 | 98% | |
OTS514 is a highly potent TOPK(T-LAK cell-originated protein kinase) inhibitor with | ||||
17030903 | Omapatrilat | 167305-00-2 | 98% | |
Omapatrilat is a novel antihypertensive agent that inhibits both neutral endopeptidas | ||||
17030902 | ON-013100 | 865783-95-5 | 98% | |
ON-013100 is a cell cycle inhibitor and is potentially useful for the treatment of ma | ||||
17030901 | ONT-093 | 216227-54-2 | 98% | |
ONT-093, also known as OC-144-093, is an orally bioavailable P-glycoprotein pump inhi | ||||
17030805 | Oxytocin | 50-56-6 | 98% | |
Oxytocin is a medication and hormone. As a medication, it is used to cause contractio | ||||
17030610 | Orteronel (racemic) | 426219-18-3 | 98% | |
Orteronel (racemic) is a mixture of S-Orteronel and R-Orteronel isomers. Orteronel, a | ||||
17022707 | Obatoclax | 803712-79-0 | 98% | |
Obatoclax (GX15-070) is Bcl-2 homology domain-3 (BH3) mimetic, antagonize all antia | ||||
17021328 | Org-26576 | 1026791-61-6;100044-96-0 | 98% | |
Org-26576 is an AMPA glutamate receptor modulator potentially for the treatment of de | ||||
17021324 | Oxyresveratrol | 29700-22-9 | 98% | |
Oxyresveratrol, a naturally occurring compound particularly found in Morus alba L., e | ||||
16122724 | ONO-7300243 | 638132-34-0 | 98% | |
ONO-7300243 is a novel, potent LPA1(Lysophosphatidic Acid Receptor) antagonist with a | ||||
16122720 | Oxolinic acid | 14698-29-4 | 98% | |
Oxolinic acid is a quinolone antibiotic, inhibiting the enzyme DNA gyrase and DNA syn | ||||
16122712 | ON123300 | 1357470-29-1 | 98% | |
ON123300 is a potent and multi-targeted kinase inhibitor with IC50 of 3.9 nM, 5 nM, 2 | ||||
16122705 | Oclacitinib | 1640292-55-2 | 98% | |
Oclacitinib is a novel inhibitor of JAK family members with IC50 ranging from 10 to 9 | ||||
6111514 | Opicapone | 923287-50-7 | 98% | |
Opicapone(BIA 9-1067) is a long-acting, peripherally selective inhibitor of catechol- | ||||
6111010 | OICR-9429 | 1801787-56-3 | 98% | |
OICR-9429 is a novel small-molecule antagonist of the Wdr5-MLL interaction with IC50 | ||||
611901 | ON 146040 | 1404231-34-0 | 98% | |
ON 146040 is the first dual PI3K and BCR-ABL inhibitor that targets the STAT3 and STA | ||||
161009007 | OSI-027 HCl salt | 936890-98-1 | 98% by HPLC | |
mTOR kinase inhibitor OSI-027 binds to and inhibits both the raptor-mTOR (TOR complex | ||||
16070915 | OtaMixaban | 193153-04-7 | 98% by HPLC | |
OtaMixaban | ||||
16070815 | Oritavancin | 171099-57-3 | 98% by HPLC | |
Oritavancin, also known as LY333328, is a novel semisynthetic glycopeptide antibiotic | ||||
1662310 | ON-01911.Na | 1330633-98-1(free base) | 98% by HPLC/HNMR | |
ON-01911.Na is a non-ATP-competitive inhibitor ofPLK1. |
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