Results for:
chemical Classification: quinazolines

Quinazoline

Compound Details

Synonymous names
QUINAZOLINE
253-82-7
Phenmiazine
1,3-Benzodiazine
1,3-Diazanaphthalene
5,6-Benzopyrimidine
Chinazolin
Benzo[a]pyrimidine
Benzopyrimidine
Benzo(a)pyrimidine
MFCD00006712
UB9QUR18NL
CHEMBL301359
CHEBI:36621
NSC-72372
Quinazolines
Quinazoline 98%
UNII-UB9QUR18NL
Benzo(e)pyrimidine
NSC72372
EINECS 205-965-3
NSC 72372
Quinazoline, 99%
4.5-Benzopyrimidine
QUINAZOLINE [MI]
SCHEMBL5920
NCIOpen2_000549
WLN: T66 BN DNJ
BIDD:GT0070
DTXSID7075214
BDBM50049572
AKOS015900554
CS-W002010
GS-3258
MCULE-5560290670
PB47603
AC-18352
SY006075
DB-046688
NS00027881
Q0055
EN300-84601
A817834
AC-907/25014195
Q426278
CU-00000000401-1
J-015972
J-524172
Z1251332997
InChI=1/C8H6N2/c1-2-4-8-7(3-1)5-9-6-10-8/h1-6
QUZ
Microorganism:

Yes

IUPAC namequinazoline
SMILESC1=CC=C2C(=C1)C=NC=N2
InchiInChI=1S/C8H6N2/c1-2-4-8-7(3-1)5-9-6-10-8/h1-6H
FormulaC8H6N2
PubChem ID9210
Molweight130.15
LogP1
Atoms10
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationquinazolines aromatic compounds benzenoids heterocyclic compounds nitrogen compounds
CHEBI-ID36621
Supernatural-IDSN0177425

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaEscherichia ColiNANADevaraj et al. 2018
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaEscherichia ColiTSATD/GC-MSno


7-bromo-6-chloro-3-[3-[(2R,3S)-3-hydroxypiperidin-2-yl]-2-oxopropyl]quinazolin-4-one

Compound Details

Synonymous names
Halofuginone
(+)-Halofuginone
Halocur
Halofuginone, (+)-
55837-20-2
6-Chloro-7-bromo-(+)-febrifugine
Halofuginon
Halofuginonum
H84E4Y7HC9
L31MM1385E
(+/-)-trans-7-bromo-6-chloro-3-(3-(3-hydroxy-2-piperidyl)-acetonyl)-4(3H)-quinazolinone
Halofuginone [INN:BAN]
7-Bromo-6-chloro-3-(3-((2R,3S)-3-hydroxy-2-piperidinyl)-2-oxopropyl)-4(3H)-quinazolinone
868851-54-1
Halofunginone
7-Bromo-6-Chloro-3-{3-[(2r,3s)-3-Hydroxypiperidin-2-Yl]-2-Oxopropyl}quinazolin-4(3h)-One
4(3H)-Quinazolinone, 7-bromo-6-chloro-3-(3-((2R,3S)-3-hydroxy-2-piperidinyl)-2-oxopropyl)-
rel-7-Bromo-6-chloro-3-(3-((2R,3S)-3-hydroxypiperidin-2-yl)-2-oxopropyl)quinazolin-4(3H)-one
NSC713205
HALOFUGINONE [INN]
Halofuginonum [INN-Latin]
Halofuginona [INN-Spanish]
UNII-L31MM1385E
HalocurTM
HT-100
7-bromo-6-chloro-3-[3-[(2R,3S)-3-hydroxy-2-piperidyl]-2-oxo-propyl]quinazolin-4-one
HFG
HALOFUGINONE [MI]
UNII-H84E4Y7HC9
SCHEMBL9541147
CHEMBL1199540
7-Bromo-6-chloro-3-[3-[(2R,3S)-3-hydroxy-2-piperidyl]-2-oxopropyl]-4(3H)-Quinazolinone
DTXSID301339439
s8144
AKOS022185424
CCG-268823
DB04866
(+-)-trans-7-Brom-6-chlor-3-(3-(3-hydroxy-2-piperidyl)acetonyl-4(3H)-chinazolinon
(+-)-trans-7-Bromo-6-chloro-3-(3-(3-hydroxy-2-piperidyl)acetonyl-4(3H)-quinazolinone
7-bromo-6-chloro-3-[3-[(2R,3S)-3-hydroxypiperidin-2-yl]-2-oxopropyl]quinazolin-4-one
trans-7-Bromo-6-chloro-3-(3-(3-hydroxy-2-piperidinyl)-2-oxopropyl)-4(3H)-quinazolinone
4(3H4(3H)-Quinazolinone, 7-bromo-6-chloro-3-(3-(3-hydroxy-2-piperidinyl)-2-oxopropyl)-, trans-(+/-)-
HALOFUGINONE [EMA EPAR VETERINARY]
rel-7-Bromo-6-chloro-3-[3-[(2R,3S)-3-hydroxy-2-piperidinyl]-2-oxopropyl]-4(3H)-quinazolinone
NS00017223
Q4132745
(+/-)-trans-7-Bromo-6-chloro-3-[3-(3-hydroxy-2-piperidinyl)-2-oxopropyl]-4(3H)-quinazolinone hydrobromide
4(3H)-Quinazolinone, 7-bromo-6-chloro-3-(3-((2R,3S)-3-hydroxy-2-piperidinyl)-2-oxopropyl)-, rel-
4(3H)-Quinazolinone, 7-bromo-6-chloro-3-(3-(3-hydroxy-2-piperidinyl)-2-oxopropyl)-, trans-
4(3H)-Quinazolinone, 7-bromo-6-chloro-3-(3-(3-hydroxy-2-piperidinyl)-2-oxopropyl)-, trans-(+-)-
4(3H)-QUINAZOLINONE, 7-BROMO-6-CHLORO-3-(3-(3-HYDROXY-2-PIPERIDINYL)-2-OXOPROPYL)-, TRANS-(+/-)-
7-bromo-6-chloro-3-{3-[(2R,3S)-3-hydroxypiperidin-2-yl]-2-oxopropyl}-3,4-dihydroquinazolin-4-one
Microorganism:

Yes

IUPAC name7-bromo-6-chloro-3-[3-[(2R,3S)-3-hydroxypiperidin-2-yl]-2-oxopropyl]quinazolin-4-one
SMILESC1CC(C(NC1)CC(=O)CN2C=NC3=CC(=C(C=C3C2=O)Cl)Br)O
InchiInChI=1S/C16H17BrClN3O3/c17-11-6-13-10(5-12(11)18)16(24)21(8-20-13)7-9(22)4-14-15(23)2-1-3-19-14/h5-6,8,14-15,19,23H,1-4,7H2/t14-,15+/m1/s1
FormulaC16H17BrClN3O3
PubChem ID456390
Molweight414.7
LogP1.4
Atoms24
Bonds4
H-bond Acceptor5
H-bond Donor2
Chemical Classificationamines quinazolines alcohols aromatic compounds halogenated compounds benzenoids bromides chlorides heterocyclic compounds ketones nitrogen compounds
Supernatural-IDSN0216206-01

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBurkholderia ArborisNANAZhu et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBurkholderia Arborisnutrient agar (NA) mediumUPLC-QTOF/MSno


6-nitro-1H-quinazoline-2,4-dione

Compound Details

Synonymous names
32618-85-2
2,4-Dihydroxy-6-nitroquinazoline
6-nitroquinazoline-2,4-diol
6-Nitro-1H-quinazoline-2,4-dione
6-nitroquinazoline-2,4(1H,3H)-dione
2,4(1H,3H)-Quinazolinedione, 6-nitro-
CHEMBL3914224
MFCD07437915
6-Nitrobenzoyleneurea
6-nitro-1,3-dihydroquinazoline-2,4-dione
SCHEMBL3025195
TWJZVXRMXVNSIE-UHFFFAOYSA-
DTXSID20355721
BCP21039
CS-D0571
BDBM50207545
STL432929
STL507399
AKOS000266271
AKOS016012995
AB05985
AC-5759
DS-5071
MCULE-4122790772
6-nitroquinazoline-2,4 (1H,3H)-dione
AM806717
BP-20257
SY046074
DB-081094
6-NITRO-2,4(1H,3H)-QUINAZOLINEDIONE
A18638
F14747
I12004
SR-01000323049
SR-01000323049-1
6-Nitroquinazoline-2,4-diol;6-Nitro-1H-quinazoline-2,4-dione
InChI=1/C8H5N3O4/c12-7-5-3-4(11(14)15)1-2-6(5)9-8(13)10-7/h1-3H,(H2,9,10,12,13)
Microorganism:

Yes

IUPAC name6-nitro-1H-quinazoline-2,4-dione
SMILESC1=CC2=C(C=C1[N+](=O)[O-])C(=O)NC(=O)N2
InchiInChI=1S/C8H5N3O4/c12-7-5-3-4(11(14)15)1-2-6(5)9-8(13)10-7/h1-3H,(H2,9,10,12,13)
FormulaC8H5N3O4
PubChem ID816982
Molweight207.14
LogP0.6
Atoms15
Bonds0
H-bond Acceptor4
H-bond Donor2
Chemical Classificationquinazolines heterocyclic compounds benzenoids nitrogen compounds aromatic compounds carbamides

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
EukaryotaSaccharomyces CerevisiaeNANAHarris et al. 2021
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
EukaryotaSaccharomyces Cerevisiaemalt extract brothHS-SPME with GC-MSno


4-methylquinazoline

Compound Details

Synonymous names
4-Methylquinazoline
700-46-9
Quinazoline, 4-methyl-
NSC-48974
NSC48974
4-methyl-quinazoline
DA8Y3UW6XP
4-Methyl-1,3-quinazoline
SCHEMBL637552
DTXSID60287113
CHEBI:207118
AMY28897
MFCD05982001
AKOS022174732
DS-11613
CS-0085114
C76230
A866693
Microorganism:

Yes

IUPAC name4-methylquinazoline
SMILESCC1=NC=NC2=CC=CC=C12
InchiInChI=1S/C9H8N2/c1-7-8-4-2-3-5-9(8)11-6-10-7/h2-6H,1H3
FormulaC9H8N2
PubChem ID241520
Molweight144.17
LogP1.4
Atoms11
Bonds0
H-bond Acceptor2
H-bond Donor0
Chemical Classificationnitrogen compounds benzenoids heterocyclic compounds aromatic compounds quinazolines
CHEBI-ID207118
Supernatural-IDSN0176939

mVOC Specific Details


Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPseudomonas AeruginosaNANABean et al. 2012
ProkaryotaPseudomonas Sp.antifungal activity against Thielaviopsis ethacetica mycelial growthBrazilian Biorenewables National Laboratory – LNBR/CNPEM Microorganism Collection, Campinas, SP; isolatedfrom soil and roots of highly productive sugarcane-producing regions; BrazilFreitas et al. 2022
ProkaryotaStreptomyces Sp.n/aNASchulz and Dickschat 2007
ProkaryotaLoktanella Sp.n/aNADickschat et al. 2005_4
ProkaryotaDinoroseobacter Shibaen/aNADickschat et al. 2005_4
ProkaryotaAchromobacter Sp.NANAAlmeida et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas Aeruginosalysogeny brothSPME/GCxGC-MSno
ProkaryotaPseudomonas Sp.DYGS mediaHS-SPME/GC-MSno
ProkaryotaStreptomyces Sp.n/an/ano
ProkaryotaLoktanella Sp.n/an/ano
ProkaryotaDinoroseobacter Shibaen/an/ano
ProkaryotaAchromobacter Sp.LB broth supplemented with cryoprotectant solution (25 g L−1 gelatin, 50 g L−1 lactose, 10 g L−1 peptone, and 250 g L−1 glycerol)SPME with gas chromatograph (Agilent 7890A, Agilent Technologies) connected to a mass spectrometer (Pegasus® HT TOFMS, LECO Corporation)no