U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C13H22N6
Molecular Weight 262.354
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ADRIFORANT

SMILES

CN[C@@H]1CCN(C1)C2=NC(N)=NC(NCC3CC3)=C2

InChI

InChIKey=ISBHYKVAFKTATD-SNVBAGLBSA-N
InChI=1S/C13H22N6/c1-15-10-4-5-19(8-10)12-6-11(17-13(14)18-12)16-7-9-2-3-9/h6,9-10,15H,2-5,7-8H2,1H3,(H3,14,16,17,18)/t10-/m1/s1

HIDE SMILES / InChI

Molecular Formula C13H22N6
Molecular Weight 262.354
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:22:17 UTC 2023
Edited
by admin
on Sat Dec 16 10:22:17 UTC 2023
Record UNII
D65H9YE9VU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ADRIFORANT
USAN   INN  
Official Name English
ZPL389-NX
Code English
NVP-ZPL389-NX
Code English
N4-(Cyclopropylmethyl)-6-[(3R)-3-(methylamino)pyrrolidin-1-yl]pyrimidine-2,4-diamine
Systematic Name English
ZPL-389-NX
Code English
PF-3893787
Code English
Adriforant [WHO-DD]
Common Name English
PF-03893787
Code English
ADRIFORANT [USAN]
Common Name English
adriforant [INN]
Common Name English
2,4-PYRIMIDINEDIAMINE, N4-(CYCLOPROPYLMETHYL)-6-((3R)-3-(METHYLAMINO)-1-PYRROLIDINYL)-
Systematic Name English
ZPL-3893787
Code English
ZPL-389
Code English
Code System Code Type Description
EVMPD
SUB194074
Created by admin on Sat Dec 16 10:22:17 UTC 2023 , Edited by admin on Sat Dec 16 10:22:17 UTC 2023
PRIMARY
FDA UNII
D65H9YE9VU
Created by admin on Sat Dec 16 10:22:17 UTC 2023 , Edited by admin on Sat Dec 16 10:22:17 UTC 2023
PRIMARY
PUBCHEM
24745335
Created by admin on Sat Dec 16 10:22:18 UTC 2023 , Edited by admin on Sat Dec 16 10:22:18 UTC 2023
PRIMARY
NCI_THESAURUS
C169765
Created by admin on Sat Dec 16 10:22:17 UTC 2023 , Edited by admin on Sat Dec 16 10:22:17 UTC 2023
PRIMARY
USAN
HI-100
Created by admin on Sat Dec 16 10:22:18 UTC 2023 , Edited by admin on Sat Dec 16 10:22:18 UTC 2023
PRIMARY
ChEMBL
CHEMBL1915540
Created by admin on Sat Dec 16 10:22:17 UTC 2023 , Edited by admin on Sat Dec 16 10:22:17 UTC 2023
PRIMARY
INN
10855
Created by admin on Sat Dec 16 10:22:17 UTC 2023 , Edited by admin on Sat Dec 16 10:22:17 UTC 2023
PRIMARY
CAS
943057-12-3
Created by admin on Sat Dec 16 10:22:17 UTC 2023 , Edited by admin on Sat Dec 16 10:22:17 UTC 2023
PRIMARY
DRUG BANK
DB15027
Created by admin on Sat Dec 16 10:22:17 UTC 2023 , Edited by admin on Sat Dec 16 10:22:17 UTC 2023
PRIMARY
SMS_ID
100000178346
Created by admin on Sat Dec 16 10:22:18 UTC 2023 , Edited by admin on Sat Dec 16 10:22:18 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY
Originator: Pfizer; Developer: Pfizer, Ziarco; Class: Anti-inflammatory, Antiasthmatic, Pyrimidine, Pyrrolidine, Small molecule; Mechanism of Action: Histamine H4 receptor antagonist; Highest Development Phases: Phase II for Atopic dermatitis, Plaque psoriasis, Discontinued for Asthma; Most Recent Event: 13 Jun 2016 Final efficacy data from a phase IIb trial in Atopic dermatitis released by Ziarco Pharma, 16 May 2016 Ziarco Pharma plans a phase IIb trial in Atopic dermatitis, 16 May 2016 Top-line efficacy and adverse events data from a phase IIa trial in Atopic dermatitis released by Ziarco Pharma