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Details

Stereochemistry ACHIRAL
Molecular Formula C19H19N5O4S
Molecular Weight 413.45
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of R-306465

SMILES

ONC(=O)C1=CN=C(N=C1)N2CCN(CC2)S(=O)(=O)C3=CC=C4C=CC=CC4=C3

InChI

InChIKey=MUTBJZVSRNUIHA-UHFFFAOYSA-N
InChI=1S/C19H19N5O4S/c25-18(22-26)16-12-20-19(21-13-16)23-7-9-24(10-8-23)29(27,28)17-6-5-14-3-1-2-4-15(14)11-17/h1-6,11-13,26H,7-10H2,(H,22,25)

HIDE SMILES / InChI

Molecular Formula C19H19N5O4S
Molecular Weight 413.45
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

R-306465 is a sulfonyl-derivative patented by Janssen Pharmaceutica N.V. as class I histone deacetylase inhibitor with broad-spectrum antitumoral activity against solid and hematological malignancies. R-306465 rapidly induced histone 3 (H3) acetylation and strongly upregulated expression of p21waf1,cip1, a downstream component of HDAC1 signaling, in A2780 ovarian carcinoma cells. R306465 showed class I HDAC isotype selectivity as evidenced by poor inhibition of HDAC6 (class IIb) confirmed by the absence of downregulation of Hsp90 chaperone c-RAF protein expression and tubulin acetylation. R306465 potently inhibited cell proliferation of all main solid tumor indications, including ovarian, lung, colon, breast and prostate cancer cell lines. Hematological cell lines, including acute lymphoblastic leukemia, acute myeloid leukemia, chronic lymphoblastic leukemia, chronic myeloid leukemia, lymphoma, and myeloma, were potently inhibited at a similar concentration range. R306465 induced apoptosis and inhibited angiogenesis in cell-based assays and had potent oral in vivo antitumoral activity in xenograft models.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
2.5 nM [IC50]
4.6 nM [IC50]
7.1 nM [IC50]
4.3 nM [IC50]
2.1 nM [IC50]
PubMed

PubMed

TitleDatePubMed
R306465 is a novel potent inhibitor of class I histone deacetylases with broad-spectrum antitumoral activity against solid and haematological malignancies.
2007 Nov 19
Patents

Sample Use Guides

The starting dose level will be 100mg/day for 21 days followed by a 1-week rest period, which constitutes a 28-day treatment cycle.
Route of Administration: Oral
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:40:09 GMT 2023
Edited
by admin
on Sat Dec 16 08:40:09 GMT 2023
Record UNII
5WD7KK1IIQ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
R-306465
Common Name English
R306465
Code English
JNJ-16241199
Code English
5-PYRIMIDINECARBOXAMIDE, N-HYDROXY-2-(4-(2-NAPHTHALENYLSULFONYL)-1-PIPERAZINYL)-
Systematic Name English
Code System Code Type Description
FDA UNII
5WD7KK1IIQ
Created by admin on Sat Dec 16 08:40:09 GMT 2023 , Edited by admin on Sat Dec 16 08:40:09 GMT 2023
PRIMARY
EPA CompTox
DTXSID00209218
Created by admin on Sat Dec 16 08:40:09 GMT 2023 , Edited by admin on Sat Dec 16 08:40:09 GMT 2023
PRIMARY
CAS
604769-01-9
Created by admin on Sat Dec 16 08:40:09 GMT 2023 , Edited by admin on Sat Dec 16 08:40:09 GMT 2023
PRIMARY
DRUG BANK
DB12382
Created by admin on Sat Dec 16 08:40:09 GMT 2023 , Edited by admin on Sat Dec 16 08:40:09 GMT 2023
PRIMARY
PUBCHEM
10309899
Created by admin on Sat Dec 16 08:40:09 GMT 2023 , Edited by admin on Sat Dec 16 08:40:09 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY