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Details

Stereochemistry ACHIRAL
Molecular Formula C30H28N2O3.ClH
Molecular Weight 501.016
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of AH-1058

SMILES

Cl.COC1=C(C(\C=C\CN2CCC(CC2)=C3C4=CC=CC=C4C=CC5=CC=CC=C35)=CC=C1)[N+]([O-])=O

InChI

InChIKey=HUGNVHKJRQLOAZ-RVDQCCQOSA-N
InChI=1S/C30H28N2O3.ClH/c1-35-28-14-6-10-25(30(28)32(33)34)11-7-19-31-20-17-24(18-21-31)29-26-12-4-2-8-22(26)15-16-23-9-3-5-13-27(23)29;/h2-16H,17-21H2,1H3;1H/b11-7+;

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C30H28N2O3
Molecular Weight 464.5549
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 1
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Effects of AH-1058, a new antiarrhythmic drug, on experimental arrhythmias and cardiac membrane currents.
1999 Apr
Antiarrhythmic and cardiohemodynamic effects of a novel Ca(2+) channel blocker, AH-1058, assessed in canine arrhythmia models.
2000 Jun 9
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 09:00:28 GMT 2023
Edited
by admin
on Sat Dec 16 09:00:28 GMT 2023
Record UNII
Z3XPW9JWMU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AH-1058
Common Name English
PIPERIDINE, 4-(5H-DIBENZO(A,D)CYCLOHEPTEN-5-YLIDENE)-1-((2E)-3-(3-METHOXY-2-NITROPHENYL)-2-PROPEN-1-YL)-, HYDROCHLORIDE (1:1)
Systematic Name English
PIPERIDINE, 4-(5H-DIBENZO(A,D)CYCLOHEPTEN-5-YLIDENE)-1-((2E)-3-(3-METHOXY-2-NITROPHENYL)-2-PROPENYL)-, MONOHYDROCHLORIDE
Systematic Name English
Code System Code Type Description
FDA UNII
Z3XPW9JWMU
Created by admin on Sat Dec 16 09:00:28 GMT 2023 , Edited by admin on Sat Dec 16 09:00:28 GMT 2023
PRIMARY
CAS
228123-15-7
Created by admin on Sat Dec 16 09:00:28 GMT 2023 , Edited by admin on Sat Dec 16 09:00:28 GMT 2023
PRIMARY
PUBCHEM
9848860
Created by admin on Sat Dec 16 09:00:28 GMT 2023 , Edited by admin on Sat Dec 16 09:00:28 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY