This is a demo store. No orders will be fulfilled.

Tucatinib (Irbinitinib, ONT-380) - 10mM in DMSO, high purity , CAS No.937263-43-9(DMSO), Receptor protein-tyrosine kinase erbB-2 inhibitor

In stock
Item Number
T408502
Grouped product items
SKU Size
Availability
Price Qty
T408502-1ml
1ml
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$302.90

HER2/ErbB2 Selective Inhibitors

View related series
Compound libraries (12325)

Basic Description

Synonyms ARRY-380 | 4,​6-​Quinazolinediamine, N6-​(4,​5-​dihydro-​4,​4-​dimethyl-​2-​oxazolyl)​-​N4-​[3-​methyl-​4-​([1,​2,​4]​triazolo[1,​5-​a]​pyridin-​7-​yloxy)​phenyl]​-
Specifications & Purity Moligand™, 10mM in DMSO
Biochemical and Physiological Mechanisms Tucatinib (Irbinitinib, ONT-380, ARRY-380) is an oral, potent, selective, reversible and ATP-competitive small-molecule inhibitor of ErbB-2 (also called HER2) with IC50s of 8 nM and 7 nM for ErbB-2 and p95 HER2, respectively in cell-based assays, showing
Storage Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Moligand™
Action Type INHIBITOR
Mechanism of action Receptor protein-tyrosine kinase erbB-2 inhibitor
Product Description

Information

Tucatinib (Irbinitinib, ONT-380, ARRY-380) is an oral, potent, selective, reversible and ATP-competitive small-molecule inhibitor ofErbB-2(also called HER2) with IC50s of 8 nM and 7 nM for ErbB-2 and p95 HER2, respectively in cell-based assays, showing ~5
In vitro

The compound is a reversible, ATP-competitive inhibitor with nanomolar potency against ErbB2 in both in vitro and in cell-based assays. Incell-based assays, ARRY-380 is ~500-fold selective for HER2 vs. EGFR and is equipotent against truncated p95-HER2.

In vivo

In vivo, ARRY-380 significantly inhibits tumor growth in multiple HER2-dependent tumor xenograft models. It shows excellent activity in numerous mouse tumor models including breast (BT-474, MDA-MB-453), ovarian (SKOV-3) and gastric (N87) carcinoma models. In the BT-474 model, ARRY-380 demonstrated significant dose-related tumor growth inhibition (TGI; 50% at 50 mg/kg/d and 96% at 100 mg/kg/d) with numerous partial regressions (>50% reduction from baseline size).
Cell Data

cell lines:Human vascular endothelial cells (HUVECs)

Concentrations:

Incubation Time:

Powder Purity:≥97%

Associated Targets(Human)

MYH14 Tchem Myosin-14 (1 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)

Names and Identifiers

Smiles CC1=CC(=CC=C1OC2=CC3=NC=N[N]3C=C2)NC4=NC=NC5=CC=C(NC6=NC(C)(C)CO6)C=C45
Molecular Weight 480.52

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Solubility Solubility (25°C) In vitro DMSO: 51 mg/mL (200.65 mM); Ethanol: 51 mg/mL (200.65 mM); Water: Insoluble;

Solution Calculators

Reviews

Customer Reviews

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.