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Details

Stereochemistry ACHIRAL
Molecular Formula C5H6N2
Molecular Weight 94.1145
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DALFAMPRIDINE

SMILES

NC1=CC=NC=C1

InChI

InChIKey=NUKYPUAOHBNCPY-UHFFFAOYSA-N
InChI=1S/C5H6N2/c6-5-1-3-7-4-2-5/h1-4H,(H2,6,7)

HIDE SMILES / InChI
Molecular Formula C5H6N2
Molecular Weight 94.1145
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:58:16 UTC 2023
Edited
by admin
on Sat Dec 16 16:58:16 UTC 2023
Record UNII
BH3B64OKL9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DALFAMPRIDINE
DASH   HSDB   II   MI   ORANGE BOOK   USAN   USP-RS   VANDF  
USAN  
Official Name English
fampridine [INN]
Common Name English
DALFAMPRIDINE [HSDB]
Common Name English
FAMPRIDINE
EMA EPAR   INN   MART.   VANDF   WHO-DD  
INN  
Official Name English
DALFAMPRIDINE [II]
Common Name English
DALFAMPRIDINE [MI]
Common Name English
4-AP
Common Name English
FAMPRIDINE [JAN]
Common Name English
FAMPRIDINE [MART.]
Common Name English
DALFAMPRIDINE [ORANGE BOOK]
Common Name English
AMPYRA
Brand Name English
DALFAMPRIDINE [USAN]
Common Name English
DALFAMPRIDINE [VANDF]
Common Name English
PYRIDIN-4-AMINE
Systematic Name English
Fampridine [WHO-DD]
Common Name English
DALFAMPRIDINE [USP MONOGRAPH]
Common Name English
FAMPRIDINE (4-AMINOPYRIDINE) [VANDF]
Common Name English
DALFAMPRIDINE [USP-RS]
Common Name English
4-PYRIDINAMINE
Systematic Name English
FAMPRIDINE [VANDF]
Common Name English
FAMPRIDINE [EMA EPAR]
Common Name English
4-Aminopyridine
Systematic Name English
EL-970
Code English
NSC-15041
Code English
FAMPYRA
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C93038
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
FDA ORPHAN DRUG 18186
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
FDA ORPHAN DRUG 214205
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
FDA ORPHAN DRUG 104497
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
EMA ASSESSMENT REPORTS FAMPYRA (AUTHORIZED: MULTIPLE SCLEROSIS)
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
EU-Orphan Drug EU/3/07/458
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
NDF-RT N0000192795
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
FDA ORPHAN DRUG 713019
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
LIVERTOX NBK548455
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
WHO-ATC N07XX07
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
WHO-VATC QN07XX07
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
EPA PESTICIDE CODE 69201
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
Code System Code Type Description
RS_ITEM_NUM
1162454
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
INN
7283
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
PUBCHEM
1727
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
DAILYMED
BH3B64OKL9
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
MERCK INDEX
m4072
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY Merck Index
HSDB
6037
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
ALANWOOD
4-aminopyridine
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
IUPHAR
2416
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
SMS_ID
100000081574
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
DRUG CENTRAL
4163
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
NCI_THESAURUS
C76777
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
USAN
FF-74
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
EPA CompTox
DTXSID0023870
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
NSC
15041
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
LACTMED
Dalfampridine
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
CAS
504-24-5
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
ECHA (EC/EINECS)
207-987-9
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
MESH
D015761
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
FDA UNII
BH3B64OKL9
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
EVMPD
SUB07505MIG
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
CHEBI
34385
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
DRUG BANK
DB06637
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
WIKIPEDIA
4-AMINOPYRIDINE
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
ChEMBL
CHEMBL284348
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY
RXCUI
897018
Created by admin on Sat Dec 16 16:58:19 UTC 2023 , Edited by admin on Sat Dec 16 16:58:19 UTC 2023
PRIMARY RxNorm
Related Record Type Details
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY B MEMBER 1
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY D MEMBER 1
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY C MEMBER 1
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY C MEMBER 2
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY A MEMBER 5
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY C MEMBER 3
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY D MEMBER 3
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY A MEMBER 2
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY A MEMBER 4
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY A MEMBER 6
TARGET -> AGONIST
Structure of 4-Aminopyridine hydrochloride
SALT/SOLVATE -> PARENT
Structure of DALFAMPRIDINE
EXCRETED UNCHANGED
URINE
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY A MEMBER 3
TARGET -> AGONIST
CYTOCHROME P450 2E1
METABOLIC ENZYME -> SUBSTRATE
MAJOR
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY A MEMBER 1
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY D MEMBER 2
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY A MEMBER 10
TARGET -> AGONIST
POTASSIUM VOLTAGE-GATED CHANNEL SUBFAMILY B MEMBER 2
TARGET -> AGONIST
Related Record Type Details
Structure of (4-AMINO-3-PYRIDYL) HYDROGEN SULFATE
METABOLITE INACTIVE -> PARENT
MAJOR
Structure of 4-AMINO-3-HYDROXYPYRIDINE
METABOLITE INACTIVE -> PARENT
MAJOR
URINE
Related Record Type Details
Structure of PYRIDIN-4-AMINE 1-OXIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
Structure of DALFAMPRIDINE
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Tmax PHARMACOKINETIC
Volume of Distribution PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
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