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Details

Stereochemistry ACHIRAL
Molecular Formula C12H9N
Molecular Weight 167.2066
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CARBAZOLE

SMILES

N1C2=C(C=CC=C2)C3=C1C=CC=C3

InChI

InChIKey=UJOBWOGCFQCDNV-UHFFFAOYSA-N
InChI=1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H

HIDE SMILES / InChI
Molecular Formula C12H9N
Molecular Weight 167.2066
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
149124
PubMed

PubMed

TitleDatePubMed
Purification of proteoglycans from mineralized tissues.
2001
Effects of polycyclic aromatic compounds on the drought tolerance of Folsomia fimetaria (Collembola, Isotomidae).
2001 Dec
Sequence-dependent binding of bis-amidine carbazole dications to DNA.
2001 Jun
Effects of eight polycyclic aromatic compounds on the survival and reproduction of the springtail Folsomia fimetaria L. (Collembola, isotomidae).
2001 Jun
Gliadin nanoparticles as carriers for the oral administration of lipophilic drugs. Relationships between bioadhesion and pharmacokinetics.
2001 Nov
X-ray diffraction and electron microscopy in the polymorphism study of ondansetron hydrochloride.
2001 Oct
Inhibition of p-cresol on aerobic biodegradation of carbazole, and sodium salicylate by Pseudomonas putida.
2002 Apr
Organization and transcriptional characterization of catechol degradation genes involved in carbazole degradation by Pseudomonas resinovorans strain CA10.
2002 Apr
Novel tricyclic-alpha-alkyloxyphenylpropionic acids: dual PPARalpha/gamma agonists with hypolipidemic and antidiabetic activity.
2002 Feb 14
Dietary exposure of finfish to aromatic contaminants and tissue distribution.
2002 May
Sphingomonas sp. strain KA1, carrying a carbazole dioxygenase gene homologue, degrades chlorinated dibenzo-p-dioxins in soil.
2002 May 21
New approaches for quantifying hyaluronic acid in pharmaceutical semisolid formulations using HPLC and CZE.
2002 Nov 7
Isolation and characterization of Sphingomonas sp. GTIN11 capable of carbazole metabolism in petroleum.
2002 Sep 20
New antimicrobial alkaloids from the roots of Polyalthia longifolia var. pendula.
2003 Apr
Degradation of carbazole, dibenzothiophene, and dibenzofuran at low temperature by Pseudomonas sp. strain C3211.
2003 Apr
[Adsorption of chondroitin sulfate-A to the surface of titanium].
2003 Dec
Determination of peptides and amino acids from wool and beer with sensitive fluorescent reagent 2-(9-carbazole)-ethyl chloroformate by reverse phase high-performance liquid chromotography and liquid chromotography mass spectrometry.
2003 Feb 1
[The synthesis and and study of cytotoxic activity of D-ribofuranosides and 2-deoxy-D-ribofuranosides of substituted bis(indolyl)furan, -pyrrole and indolo[2,3-alpha]carbazole derivatives].
2003 Mar-Apr
Purification and characterization of 2'aminobiphenyl-2,3-diol 1,2-dioxygenase from Pseudomonas sp. LD2.
2003 Nov
Polarization holographic gratings in hybrid solgel films doped with Disperse Red 1.
2003 Nov 15
High-performance blue electroluminescent devices based on 2-(4-biphenylyl)-5-(4-carbazole-9-yl)phenyl-1,3,4-oxadiazole.
2003 Nov 7
Total synthesis of carbazoquinocin C: application of the o-benzannulation of Fischer carbene complexes to carbazole-3,4-quinone alkaloids.
2004 Feb 5
Mechanism of mahanine-induced apoptosis in human leukemia cells (HL-60).
2004 Jan 1
Patents

Patents

JP2000086921A
1
JP2000229943A
1
JP2000245445A
1
JP2001220578A
1
JP2003334569A
1
JP2004071380A
1
JP2004178895A
1
JP2004277404A
1
JP2004315545A
2
JP2004363103A
1
JP2004531594A
7
JP2004534046A
7
JP2005060524A
1
JP2005113043A
1
JP2005290000A
1
JP2006191138A
1
JP2007045816A
1
JP2007112930A
1
JP2007119354A
1
JP2007142111A
1
JP2007297540A
1
JP2007308376A
1
JP2008031145A
1
JP2008085079A
1
JP2008098433A
1
JP2008127387A
1
JP2009091462A
1
JP2009294620A
1
JP2010073987A
1
JP2010189588A
1
JP2010533228A
6
JP5355421B2
2
JP5376063B2
1
JPH01108279A
1
JPH02127432A
1
JPH02165155A
1
JPH03185484A
1
JPH03251552A
1
JPH041207A
1
JPH04180923A
1
JPH04230385A
1
JPH04288057A
1
JPH04316543A
4
JPH06104470A
1
JPH0656777A
1
JPH08175991A
1
JPH09211874A
1
JPH09295969A
1
JPH0948758A
1
JPH1059939A
1
JPH11329737A
1
Substance Class Chemical
Created
by admin
on Mon Mar 31 17:45:08 GMT 2025
Edited
by admin
on Mon Mar 31 17:45:08 GMT 2025
Record UNII
0P2197HHHN
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CARBAZOLE
HSDB   MI  
Systematic Name English
CARPROFEN RELATED COMPOUND A
USP   USP-RS  
Preferred Name English
NSC-3498
Code English
DIBENZOPYRROLE
Systematic Name English
CARBAZOLE [MI]
Common Name English
CARBAZOLE [HSDB]
Common Name English
CARPROFEN RELATED COMPOUND A [USP-RS]
Common Name English
CARPROFEN RELATED COMPOUND A [USP IMPURITY]
Common Name English
CARBAZOLE [IARC]
Common Name English
9H-CARBAZOLE
Systematic Name English
Code System Code Type Description
WIKIPEDIA
CARBAZOLE
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
HSDB
2164
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
DRUG BANK
DB07301
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
CHEBI
27543
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
MERCK INDEX
m3061
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY Merck Index
CHEBI
3391
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
PUBCHEM
6854
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
RS_ITEM_NUM
1096702
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
CAS
86-74-8
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
FDA UNII
0P2197HHHN
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
NSC
3498
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
MESH
C041514
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
ECHA (EC/EINECS)
201-696-0
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID4020248
Created by admin on Mon Mar 31 17:45:08 GMT 2025 , Edited by admin on Mon Mar 31 17:45:08 GMT 2025
PRIMARY
Related Record Type Details
Structure of CARPROFEN
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
NIH
NCATS
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