SBI-0206965 - 98%, high purity , CAS No.1884220-36-3, Inhibitor of unc-51 like autophagy activating kinase 1

Item Number
S413863
Grouped product items
SKUSizeAvailabilityPrice Qty
S413863-5mg
5mg
Available within 1-2 weeks(?)
Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$75.90
S413863-10mg
10mg
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Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$129.90
S413863-25mg
25mg
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Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$292.90
S413863-50mg
50mg
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Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$380.90
S413863-100mg
100mg
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Item is derived from our semi-finished stock and is processed in 1-2 weeks.
$597.90

ULK Inhibitors

Basic Description

SynonymsAS-56287 | GTPL11339 | 2-(5-Bromo-2-(3,4,5-trimethoxyphenylamino)pyrimidin-4-yloxy)-N-methylbenzamide | 4-oxocyclohexylcarboxylic acid ethyl ester | HY-16966 | NSC784816 | NSC-784816 | SBI 0206965 | US10266549, Example 171a | US10266549, Example 88 | CCG-
Specifications & PurityMoligand™, ≥98%
Biochemical and Physiological MechanismsSBI-0206965 is a highly selective autophagy kinase ULK1 inhibitor with IC50 of 108 nM, about 7-fold selectivity over ULK2. SBI-0206965 inhibits autophagy and enhances apoptosis in human glioblastoma and lung cancer cells.
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of unc-51 like autophagy activating kinase 1
Product Description

Information

SBI-0206965 SBI-0206965 is a highly selective autophagy kinase ULK1 inhibitor with IC50 of 108 nM, about 7-fold selectivity over ULK2. SBI-0206965 inhibits autophagy and enhances apoptosis in human glioblastoma and lung cancer cells.


Targets

ULK1 (Cell-free assay); ULK2 (Cell-free assay) 108 nM; 711 nM


In vitro

In HEK293T transfected with WT or KI Myc-tagged ULK1 and WT Vps34, SBI-0206965 inhibits Ser249 phosphorylation of overexpressed Vps34 and Beclin1 Ser15 phosphorylation. SBI-0206965 suppresses autophagy induced by mTOR inhibition in A549 cells, and prevents ULK1-dependent cell survival in WT MEFs. In addition, SBI-0206965 also synergizes with mTOR inhibition to induce cancer cell death.

Product Properties

ALogP4.128
HBD Count2
Rotatable Bond8

Associated Targets(Human)

ULK1 Tchem Serine/threonine-protein kinase ULK1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ULK2 Tchem Serine/threonine-protein kinase ULK2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
HL-60 (67320 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MCF7 (126967 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MDA-MB-468 (9477 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
U-937 (7138 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ULK2 Tchem Serine/threonine-protein kinase ULK2 (652 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 2-[5-bromo-2-(3,4,5-trimethoxyanilino)pyrimidin-4-yl]oxy-N-methylbenzamide
INCHI InChI=1S/C21H21BrN4O5/c1-23-19(27)13-7-5-6-8-15(13)31-20-14(22)11-24-21(26-20)25-12-9-16(28-2)18(30-4)17(10-12)29-3/h5-11H,1-4H3,(H,23,27)(H,24,25,26)
InChi Key NEXGBSJERNQRSV-UHFFFAOYSA-N
Canonical SMILES CNC(=O)C1=CC=CC=C1OC2=NC(=NC=C2Br)NC3=CC(=C(C(=C3)OC)OC)OC
Isomeric SMILES CNC(=O)C1=CC=CC=C1OC2=NC(=NC=C2Br)NC3=CC(=C(C(=C3)OC)OC)OC
PubChem CID 92044402
Molecular Weight 489.32

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

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10 results found

Lot NumberCertificate TypeDateItem
D2312677Certificate of AnalysisMar 02, 2023 S413863
D2313474Certificate of AnalysisMar 02, 2023 S413863
D2313476Certificate of AnalysisMar 02, 2023 S413863
D2313477Certificate of AnalysisMar 02, 2023 S413863
D2313478Certificate of AnalysisMar 02, 2023 S413863
D2313479Certificate of AnalysisMar 02, 2023 S413863
D2313481Certificate of AnalysisMar 02, 2023 S413863
D2313482Certificate of AnalysisMar 02, 2023 S413863
D2313483Certificate of AnalysisMar 02, 2023 S413863
D2313484Certificate of AnalysisMar 02, 2023 S413863

Chemical and Physical Properties

SolubilitySolubility (25°C) In vitro DMSO: 97 mg/mL (198.23 mM); Ethanol: 20 mg/mL warmed with 50ºC Water: bath (40.87 mM); Water: Insoluble;
DMSO(mg / mL) Max Solubility97
DMSO(mM) Max Solubility198.2342843
Water(mg / mL) Max Solubility<1

Safety and Hazards(GHS)

Pictogram(s) GHS07
Signal Warning
Hazard Statements

H315:Causes skin irritation

H319:Causes serious eye irritation

H335:May cause respiratory irritation

Precautionary Statements

P261:Avoid breathing dust/fume/gas/mist/vapors/spray.

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352:IF ON SKIN: wash with plenty of water.

P321:Specific treatment (see ... on this label).

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P271:Use only outdoors or in a well-ventilated area.

P304+P340:IF INHALED: Remove person to fresh air and keep comfortable for breathing.

P403+P233:Store in a well-ventilated place. Keep container tightly closed.

P362+P364:Take off contaminated clothing and wash it before reuse.

P264+P265:Wash hands [and …] thoroughly after handling. Do not touch eyes.

P337+P317:If eye irritation persists: Get medical help.

P332+P317:If skin irritation occurs: Get medical help.

P319:Get medical help if you feel unwell.

Related Documents

References

1. Egan DF, Chun MG, Vamos M, Zou H, Rong J, Miller CJ, Lou HJ, Raveendra-Panickar D, Yang CC, Sheffler DJ et al..  (2015)  Small Molecule Inhibition of the Autophagy Kinase ULK1 and Identification of ULK1 Substrates..  Mol Cell,  59  (2): (285-97).  [PMID:26118643] [10.1021/op500134e]

Solution Calculators