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Details

Stereochemistry ACHIRAL
Molecular Formula C18H15ClN6OS2
Molecular Weight 430.934
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SNS-314

SMILES

ClC1=CC(NC(=O)NC2=NC=C(CCNC3=C4SC=CC4=NC=N3)S2)=CC=C1

InChI

InChIKey=FAYAUAZLLLJJGH-UHFFFAOYSA-N
InChI=1S/C18H15ClN6OS2/c19-11-2-1-3-12(8-11)24-17(26)25-18-21-9-13(28-18)4-6-20-16-15-14(5-7-27-15)22-10-23-16/h1-3,5,7-10H,4,6H2,(H,20,22,23)(H2,21,24,25,26)

HIDE SMILES / InChI

Molecular Formula C18H15ClN6OS2
Molecular Weight 430.934
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

SNS 314 is a selective small molecule inhibitor of Aurora kinases A, B and C. The compound was being developed by Sunesis Pharmaceuticals for the treatment of cancer. Proliferating cells treated with SNS-314 bypass the mitotic spindle checkpoint and fail to undergo cytokinesis, leading to multiple rounds of endoreduplication and eventually cell death. SNS-314 inhibits tumor growth in a variety of preclinical models, and it was being tested in single agent Phase 1 studies in patients with advanced solid tumours.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: O14965
Gene ID: 6790.0
Gene Symbol: AURKA
Target Organism: Homo sapiens (Human)
9.0 nM [IC50]
Target ID: Q96GD4|||O60446
Gene ID: 9212.0
Gene Symbol: AURKB
Target Organism: Homo sapiens (Human)
31.0 nM [IC50]
Target ID: Q9UQB9
Gene ID: 6795.0
Gene Symbol: AURKC
Target Organism: Homo sapiens (Human)
3.4 nM [IC50]
Target ID: P04629|||Q7Z5C3
Gene ID: 4914.0
Gene Symbol: NTRK1
Target Organism: Homo sapiens (Human)
12.0 nM [IC50]
Target ID: Q16620
Gene ID: 4915.0
Gene Symbol: NTRK2
Target Organism: Homo sapiens (Human)
5.0 nM [IC50]
AUC

AUC

ValueDoseCo-administeredAnalytePopulation
2090 ng × h/mL
5 mg/kg single, intravenous
dose: 5 mg/kg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
SNS-314 plasma
Rattus norvegicus
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
3650 ng × h/mL
10 mg/kg single, oral
dose: 10 mg/kg
route of administration: Oral
experiment type: SINGLE
co-administered:
SNS-314 plasma
Rattus norvegicus
population: HEALTHY
age: ADULT
sex: MALE
food status: UNKNOWN
T1/2

T1/2

ValueDoseCo-administeredAnalytePopulation
1.4 h
5 mg/kg single, intravenous
dose: 5 mg/kg
route of administration: Intravenous
experiment type: SINGLE
co-administered:
SNS-314 plasma
Mus musculus
population: HEALTHY
age: ADULT
sex: UNKNOWN
food status: UNKNOWN
PubMed

PubMed

TitleDatePubMed
Targeting high Aurora kinases expression as an innovative therapy for hepatocellular carcinoma.
2017-04-25
SNS-314, a pan-Aurora kinase inhibitor, shows potent anti-tumor activity and dosing flexibility in vivo.
2010-03
Discovery of a potent and selective aurora kinase inhibitor.
2008-09-01
Patents

Patents

Sample Use Guides

Mice: In the HCT116 human colon cancer xenograft model, administration of 50 and 100 mg/kg SNS-314 led to dose-dependent inhibition of histone H3 phosphorylation for at least 10 h, indicating effective Aurora-B inhibition in vivo.
Route of Administration: Intraperitoneal
SNS-314 Mesylate is a potent and selective inhibitor of Aurora A, Aurora B and Aurora C with IC50 of 9 nM, 31 nM, and 3 nM, respectively and less potent to Trk A/B, Flt4, Fms, Axl, c-Raf and DDR2.
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:24:08 GMT 2025
Edited
by admin
on Mon Mar 31 18:24:08 GMT 2025
Record UNII
802IFJ0Z8X
Record Status Validated (UNII)
Record Version
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Name Type Language
SNS-314
Common Name English
SNS 314 [WHO-DD]
Preferred Name English
UREA, N-(3-CHLOROPHENYL)-N'-(5-(2-(THIENO(3,2-D)PYRIMIDIN-4-YLAMINO)ETHYL)-2-THIAZOLYL)-
Systematic Name English
Code System Code Type Description
NCI_THESAURUS
C70655
Created by admin on Mon Mar 31 18:24:08 GMT 2025 , Edited by admin on Mon Mar 31 18:24:08 GMT 2025
PRIMARY
ChEMBL
CHEMBL482767
Created by admin on Mon Mar 31 18:24:08 GMT 2025 , Edited by admin on Mon Mar 31 18:24:08 GMT 2025
PRIMARY
PUBCHEM
24995524
Created by admin on Mon Mar 31 18:24:08 GMT 2025 , Edited by admin on Mon Mar 31 18:24:08 GMT 2025
PRIMARY
FDA UNII
802IFJ0Z8X
Created by admin on Mon Mar 31 18:24:08 GMT 2025 , Edited by admin on Mon Mar 31 18:24:08 GMT 2025
PRIMARY
DRUG BANK
DB06134
Created by admin on Mon Mar 31 18:24:08 GMT 2025 , Edited by admin on Mon Mar 31 18:24:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID20147269
Created by admin on Mon Mar 31 18:24:08 GMT 2025 , Edited by admin on Mon Mar 31 18:24:08 GMT 2025
PRIMARY
CAS
1057249-41-8
Created by admin on Mon Mar 31 18:24:08 GMT 2025 , Edited by admin on Mon Mar 31 18:24:08 GMT 2025
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY