Results for:
chemical Classification: Flavonoides

3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one

Compound Details

Synonymous names
Pelargidenolon
Pelargidenon
Rhamnolutein
kaempferol
Kaempherol
Nimbecetin
Populnetin
Rhamnolutin
Trifolitin
Campherol
IYRMWMYZSQPJKC-UHFFFAOYSA-N
Kaemferol
Kaempferol, primary pharmaceutical reference standard
Kampcetin
Kampferol
Kampherol
Kempferol
Robigenin
Swartziol
Indigo Yellow
Kaempferol-Supplied by Selleck Chemicals
Kaempferol, analytical standard
4det
AC1NQXP1
5,4'-Trihydroxyflavonol
CHEMBL150
Pelargidenolon 1497
BDBM7462
CCRIS 41
CK0011
GP7425
SCHEMBL18817
HMDB05801
K0018
N1719
S2314_Selleck
W1682
3,5,7-Tetrahydroxyflavone
5,7,4'-Trihydroxyflavonol
AC-544
BIDD:ER0134
BIDD:PXR0073
DB01852
Kaempferol, United States Pharmacopeia (USP) Reference Standard
LS-176
TNP00039
731P2LE49E
C05903
DSSTox_CID_768
HMS1571K18
HMS2098K18
HMS2267I09
HMS3656M03
HSDB 7703
J10449
BC215517
BT000416
CS-1273
DNC006613
DTXSID7020768
GS-3570
HE004319
HE279342
HE347988
NSC407289
NSC656277
SBB066091
ST030560
A828886
CHEBI:28499
UNII-731P2LE49E
W-2776
ZINC3869768
AB0010534
AN-15750
BSPBio_001176
CC-29746
DSSTox_GSID_20768
HY-14590
KB-79581
SC-17291
3,4',5,7-Tetrahydroxyflavone
C-18018
DSSTox_RID_75781
LMPK12110003
MFCD00016938
Prestwick0_001098
Prestwick1_001098
Prestwick2_001098
Prestwick3_001098
SPBio_003058
ZINC03869768
3,4,5,7-Tetrahydroxyflavone
AB00514046
AI3-36096
CCG-202823
NSC 407289
NSC 656277
NSC-407289
NSC-656277
TR-018501
3,4′,5,7-Tetrahydroxyflavone
ACon1_001867
AKOS015895240
BPBio1_001294
Flavone,4',5,7-tetrahydroxy-
HSCI1_000027
I06-0240
MEGxp0_001283
Oprea1_650954
Q-100584
BRN 0304401
cid_5280863
FT-0614420
MLS000697730
MLS001055391
MLS001074884
MLS006010737
SMR000112585
Tox21_201165
Tox21_303363
520-18-3
C.I. 75640
Kaempferol, >=90% (HPLC), powder
Kaempferol, >=97.0% (HPLC)
MCULE-8965218413
NCGC00016480-01
NCGC00016480-02
NCGC00016480-03
NCGC00016480-04
NCGC00016480-05
NCGC00016480-06
NCGC00016480-07
NCGC00016480-09
NCGC00091036-01
NCGC00091036-02
NCGC00164322-01
NCGC00179275-01
NCGC00179275-02
NCGC00257464-01
NCGC00258717-01
CAS-520-18-3
EINECS 208-287-6
KAEMPFEROL ROBIGENIN; 3,4',5,7-TETRAHYDRO-XY-FLAVONE
Flavone, 3,4',5,7-tetrahydroxy-
MolPort-001-741-568
3,4',5,7-tetrahydroxy-Flavone (7CI,8CI)
3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one
5-18-05-00251 (Beilstein Handbook Reference)
Kaempferol|Kempferol|3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-chromen-4-one
BRD-K12807006-001-05-2
2-(4-hydroxyphenyl)-3,5,7-tris(oxidanyl)chromen-4-one
3,?5,?7-?TRIHYDROXY-?2-?(4-?HYDROXYPHENYL)-?4H-?1-?BENZOPYRAN-?4-?ONE
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-1-benzopyran-4-one
Flavone, 3,4',5,7-tetrahydroxy- (7CI,8CI)
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one
4H-1-Benzopyran-4-one,5,7-trihydroxy-2-(4-hydroxyphenyl)-
A91A6666-86C8-4B33-B3EF-F74CD3CD7F47
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one #
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
3,5,7-trihydroxy-2-(4-hydroxyphenyl)-4H-1- benzopyran-4-one
3,5,7-Trihydroxy-2-[4-hydroxy-phenyl]-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one,3,5,7-trihydroxy-2-(4-hydroxyphenyl)-
3,5,7-Trihydroxy-2-[4-hydroxy- phenyl]-4H-1-benzopyran-4-one
4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-
4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)-5,7,4'-Trihydroxyflavonol
4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(4-hydroxyphenyl)- (9CI)
Microorganism:

Yes

IUPAC name3,5,7-trihydroxy-2-(4-hydroxyphenyl)chromen-4-one
SMILESC1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O
InchiInChI=1S/C15H10O6/c16-8-3-1-7(2-4-8)15-14(20)13(19)12-10(18)5-9(17)6-11(12)21-15/h1-6,16-18,20H
FormulaC15H10O6
PubChem ID5280863
Molweight286.239
LogP2.46
Atoms31
Bonds33
H-bond Acceptor6
H-bond Donor4
Chemical ClassificationFlavonoides alcohols benzenoids ethers

mVOC Specific Details

Solubility
Soluble in hot alcohol, ether or alkalies
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 2006., p. 913
Literature: #Insoluble in benzene; slightly soluble in chloroform; soluble in acetic acid, alkalies; very soluble in ethanol, ethyl ether, acetone
Literature: Lide, D.R., G.W.A. Milne (eds.). Handbook of Data on Organic Compounds. Volume I. 3rd ed. CRC Press, Inc. Boca Raton ,FL. 1994., p. V2: 1583
Literature: #In water, 440 mg/L at 25 deg C (est)
Literature: US EPA; Estimation Program Interface (EPI) Suite. Ver.3.20. February, 2007. Available from, as of January 22, 2009: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
Vapor Pressure
PressureReference
1.1X10-13mm Hg at 25 deg C (est)US EPA; Estimation Program Interface (EPI) Suite. Ver.3.20. February, 2007. Available from, as of Jan 19, 2009: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
MS-Links
MS-MS Spectrum 6076 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Negative
MS-MS Spectrum 2449 - Quattro_QQQ 25V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 6077 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Negative
MS-MS Spectrum 6073 - EI-B (JEOL JMS-06-H) Positive
MS-MS Spectrum 201967
MS-MS Spectrum 179923
MS-MS Spectrum 201962
MS-MS Spectrum 2448 - Quattro_QQQ 10V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 182258
MS-MS Spectrum 201966
MS-MS Spectrum 6082 - LC-ESI-ITTOF (LCMS-IT-TOF) Negative
MS-MS Spectrum 201964
MS-MS Spectrum 6079 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Positive
MS-MS Spectrum 201961
MS-MS Spectrum 6081 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Negative
MS-MS Spectrum 179922
MS-MS Spectrum 179924
MS-MS Spectrum 2450 - Quattro_QQQ 40V Positive delivery=Flow_Injection analyzer=Triple_Quad
MS-MS Spectrum 201965
MS-MS Spectrum 201963
MS-MS Spectrum 182256
MS-MS Spectrum 6075 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) 5V Positive
MS-MS Spectrum 6080 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Positive
MS-MS Spectrum 6078 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Positive
MS-MS Spectrum 182257
1D-NMR-Links

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiGanoderma LucidumnaKoreaKim et al., 2008
FungiInonotus ObliquusnaKoreaKim et al., 2008
FungiSparassis CrispanaKoreaKim et al., 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiGanoderma LucidumnaHPLCYes
FungiInonotus ObliquusnaHPLCYes
FungiSparassis CrispanaHPLCYes


3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one

Compound Details

Synonymous names
Cannabiscetin
IKMDFBPHZNJCSN-UHFFFAOYSA-N
myricetin
Myricetol
Myricitin
Myricetin, primary pharmaceutical reference standard
MYC
Myricetin-Supplied by Selleck Chemicals
Myricetin, analytical standard
4gqr
AC1NQYV4
CHEMBL164
76XC01FTOJ
Myricetin from Myrica cerifera leaf and bark
2o63
Prestwick_342
BS0289
CM0160
GL5441
SCHEMBL19302
UNII-76XC01FTOJ
BDBM15236
HMDB02755
M2131
Myricetin, Cannabiscetin, Myricetol, Myricitin)
N1850
S2326_Selleck
AN-939
BIDD:ER0142
BIDD:PXR0079
DB02375
LP00740
TNP00286
C10107
CCRIS 5838
HMS1569M12
HMS2096M12
HMS2231L04
HMS3262C22
HMS3656I05
HSDB 7682
S00115
AC-4533
AK111247
BBL023468
BC201817
Bio-0838
BT000486
CS-6221
DR001388
DTXSID8022400
HE280297
HE349008
KS-5268
NSC407290
ST057235
STL284709
A829320
CHEBI:18152
M 6760
M-1214
SpecPlus_000531
Spectrum_001501
ZINC3874317
4CN-1085
AB0149714
AJ-46397
AX8140581
BSPBio_000570
HY-15097
KBioGR_001884
KBioSS_001981
Lopac-M-6760
LS-69005
LMPK12110001
MFCD00006827
Prestwick0_000465
Prestwick1_000465
Prestwick2_000465
Prestwick3_000465
SPBio_002509
Spectrum4_001272
Spectrum5_000692
ZINC03874317
CCG-204825
Myricetin, >=96.0%, crystalline
NSC 407290
NSC-407290
ST24041172
TR-018746
ACon1_000267
AKOS015903103
BPBio1_000628
DivK1c_006627
KBio1_001571
KBio2_001981
KBio2_004549
KBio2_007117
Lopac0_000740
MEGxp0_000357
Q-100601
BRN 0332331
cid_5281672
EU-0100740
FT-0672573
MLS002153825
MLS006010718
SMR001233193
I14-19097
NCI60_003870
Tox21_500740
3,7,3',4',5'-Hexahydroxyflavone
529-44-2
REGID_for_CID_5281672
MCULE-6299186219
Myricetin, >=96.0% (HPLC)
NCGC00015697-01
NCGC00015697-02
NCGC00015697-03
NCGC00015697-04
NCGC00015697-05
NCGC00015697-06
NCGC00015697-07
NCGC00015697-08
NCGC00015697-09
NCGC00015697-10
NCGC00015697-11
NCGC00015697-12
NCGC00015697-13
NCGC00094083-01
NCGC00094083-02
NCGC00094083-03
NCGC00094083-04
NCGC00179517-01
NCGC00179517-02
NCGC00261425-01
CAS-529-44-2
EINECS 208-463-2
3,3',4',5,5',7-Hexahydroxyflavone
3,5,7,3',4',5'-Hexahydroxyflavone
MolPort-001-740-532
Flavone,3',4',5,5',7-hexahydroxy-
3,3',4',5,5',7-hexOH-Flavone
C07E0ED2-ABF6-4BD3-A2B2-A98CAEF20FD1
FLAVONE, 3,3',4',5,5',7-HEXAHYDROXY-
3,3 ,4 ,5,5 ,7-Hexahydroxyflavone
BRD-K43149758-001-04-5
3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one
3,3',4',5,5',7-hexahydroxy-(8CI)- flavone
3,3',4,4',5',7-Hexahydro-2-phenyl-4H-chromen-4-one
3,?5,?7-?TRIHYDROXY-?2-?(3,?4,?5-?TRIHYDROXYPHENYL)-?4H-?1-?BENZOPYRAN-?4-?ONE
3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-1-benzopyran-4-one
3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one
4H-1-Benzopyran-4-one,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-
3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-chromen-4-one #
2-(3,4,5-TRIHYDROXYPHENYL)-3,5,7-TRIHYDROXY-4H-1-BENZOPYRAN-4-ONE
3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one
3,5,7-tris(oxidanyl)-2-[3,4,5-tris(oxidanyl)phenyl]chromen-4-one
4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-
4H-1-Benzopyran-4-one, 3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)- (9CI)
Microorganism:

Yes

IUPAC name3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one
SMILESC1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O
InchiInChI=1S/C15H10O8/c16-6-3-7(17)11-10(4-6)23-15(14(22)13(11)21)5-1-8(18)12(20)9(19)2-5/h1-4,16-20,22H
FormulaC15H10O8
PubChem ID5281672
Molweight318.237
LogP1.85
Atoms33
Bonds35
H-bond Acceptor8
H-bond Donor6
Chemical ClassificationFlavonoides alcohols benzenoids ethers

mVOC Specific Details

Solubility
Sparingly soluble in boiling water; soluble in alcohol. Practically insoluble in chloroform, acetic acid
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 2006., p. 1095
Literature: #In water, 54.9 mg/L at 25 deg C (est)
Literature: US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.0. Jan, 2009. Available from, as of Feb 4, 2009: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
Vapor Pressure
PressureReference
6.84X10-17 mm Hg at 25 deg C (est)US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.0. Jan, 2009. Available from, as of Feb 4, 2009: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
MS-Links
MS-MS Spectrum 202028
MS-MS Spectrum 202031
MS-MS Spectrum 20797
MS-MS Spectrum 20795
MS-MS Spectrum 22346
MS-MS Spectrum 202033
MS-MS Spectrum 6372 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) 5V Positive
MS-MS Spectrum 202030
MS-MS Spectrum 202036
MS-MS Spectrum 6377 - LC-ESI-ITTOF (LCMS-IT-TOF) Positive
MS-MS Spectrum 202027
MS-MS Spectrum 22348
MS-MS Spectrum 6378 - LC-ESI-ITTOF (LCMS-IT-TOF) Negative
MS-MS Spectrum 6376 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Positive
MS-MS Spectrum 202029
MS-MS Spectrum 22347
MS-MS Spectrum 6373 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Negative
MS-MS Spectrum 6374 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Negative
MS-MS Spectrum 20796
MS-MS Spectrum 202037
MS-MS Spectrum 202032
MS-MS Spectrum 202026
MS-MS Spectrum 202035
MS-MS Spectrum 202034
MS-MS Spectrum 6375 - LC-ESI-QTOF (UPLC Q-Tof Premier, Waters) Positive

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAgaricus BisporusnaKoreaKim et al., 2008
FungiAgaricus BlazeinaKoreaKim et al., 2008
FungiGanoderma LucidumnaKoreaKim et al., 2008
FungiPleurotus OstreatusnaKoreaKim et al., 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiAgaricus BisporusnaHPLCYes
FungiAgaricus BlazeinaHPLCYes
FungiGanoderma LucidumnaHPLCYes
FungiPleurotus OstreatusnaHPLCYes


5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one

Mass-Spectra

Compound Details

Synonymous names
naringenin
Naringenine
naringetol
salipurpol
FTVWIRXFELQLPI-UHFFFAOYSA-N
NARIGENIN
Narngenn
Salipurol
rac Naringenin
AC1L1ACN
AC1Q6KJD
4',7-Trihydroxyflavanone
naringenin-7-sulfate
K702
Naringenin (NAR)
pelargidanon 1602
Prestwick_531
( inverted exclamation markA)-Naringenin
(S)-Naringenin
BN0800
CHEMBL32571
CN0031
Naringenin, 90%
SCHEMBL20571
4',5,7-Trihydroxyflavanone
5,7,4'-Trihydroxyflavanone
BDBM19461
CTK7J9188
N0072
NSC11855
NSC34875
RL05877
(R,S)-Naringenin
CCRIS 8135
HMS1569M14
HMS2096M14
HMS2231O18
HMS3352B08
HMS3373N07
HMS3656G15
S00279
(-)-Naringenin
AK122638
DR000876
Flavanone,5,7-trihydroxy-
HE279447
KS-5142
LS-5089
Opera_ID_106
SBB006461
SCHEMBL1934259
ST057236
CHEBI:50202
M-7677
4 ,5,7-Trihydroxyflavanone
4CN-0924
AB1003941
AB1009825
AC-20273
AN-45184
ANW-43843
AX8246816
BE 14348A
BE-14348A
BSPBio_000572
DTXSID50274239
LS-39547
NSC 11855
NSC 34875
NSC-11855
NSC-34875
SC-18078
ST2418556
Prestwick0_000466
Prestwick1_000466
Prestwick2_000466
Prestwick3_000466
SPBio_002511
ZX-AT026530
KB-187979
KB-196356
TR-017609
TR-037462
ACon1_000582
AKOS015895052
BPBio1_000630
I06-0445
I06-0536
J-523457
MEGxp0_000358
Oprea1_194140
Q-100521
4CH-012369
FT-0082287
FT-0630981
MLS000028739
MLS000738094
MLS001146907
SMP1_000060
SMR000059039
(+/-)-Naringenin
480-41-1
Flavanone, 4',5,7-trihydroxy-
(+/-)-Naringenin, analytical standard
MCULE-5489217450
Naringenin, natural (US), 98%
NCGC00017346-02
NCGC00017346-03
NCGC00017346-04
NCGC00095963-01
NCGC00095963-02
NCGC00095963-03
EINECS 207-550-2
EINECS 266-769-1
67604-48-2
93602-28-9
MolPort-000-861-091
AE-848/32605045
(+/-)-Naringenin, >=95%
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one
(+/-)-5,7,4'-Trihydroxyflavanone
5,7-Dihydroxy-2-(4-hydroxy-phenyl)-chroman-4-one
(+/-)-Naringenin, ~95% (HPCE)
BRD-A94669766-001-02-6
BRD-A94669766-001-04-2
5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one
2S,?3-?DIHYDRO-?5,?7-?DIHYDROXY-?2-?(4-?HYDROXYPHENYL)-?4H-?1-?BENZOPYRAN-?4-?ONE
5,7-Dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one
(S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-4-benzopyrone
4H-1-Benzopyran-4-one,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-
( )-Naringenin; 4?,5,7-Trihydroxyflavanone; H-1-benzopyran-4-one
2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one
EC19096C-4404-4A16-9BF9-92F9F358E005
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-
4H-1-Benzopyran-4-one,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-, (S)-
5,7-Dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one, (S)- #
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-, (S)-
( inverted exclamation markA)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one; 4 inverted exclamation marka,5,7-Trihydroxyflavanone
Microorganism:

Yes

IUPAC name5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one
SMILESC1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O
InchiInChI=1S/C15H12O5/c16-9-3-1-8(2-4-9)13-7-12(19)15-11(18)5-10(17)6-14(15)20-13/h1-6,13,16-18H,7H2
FormulaC15H12O5
PubChem ID932
Molweight272.256
LogP2.84
Atoms32
Bonds34
H-bond Acceptor5
H-bond Donor3
Chemical ClassificationFlavonoides alcohols benzenoids ethers

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiSparassis CrispanaKoreaKim et al., 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiSparassis CrispanaHPLCYes


(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one

Compound Details

Synonymous names
Naringenine-7-rhamnosidoglucoside
Naringoside
naringin
aurantiin
Naringin hydrate
Naringenin 7-Rhamnoglucoside
Naringenin-7-beta-neohesperidoside
Naringin-Supplied by Selleck Chemicals
Naringenin 7-O-neohesperidoside
AC1L9CSZ
Naringin, Naringoside, Naringenine-7-rhamnosidoglucoside
yphenyl)chroman-4-one
GTPL4738
SCHEMBL23432
N2371
N7TD9J649B
S2329_Selleck
HMS500M09
HMDB02927
BIDD:ER0262
CHEMBL451532
HMS2231M18
J10148
C09789
UNII-N7TD9J649B
(2S)-Naringin
CA006180
DTXSID6022478
DR003314
HY-N0153
CS-5632
C27H32O14
BT000958
ST072162
ZINC8143604
CHEBI:28819
cid_25075
CC-32461
BSPBio_000574
STOCK1N-40898
4'5-diOH-Flavone-7-rhgluc
NINDS_000247
SPBio_002513
C-23277
Prestwick3_000467
BDBM50241582
Prestwick2_000467
Prestwick1_000467
Prestwick0_000467
CCG-208591
cid_442428
AI3-19008
KBio1_000247
MEGxp0_001877
DivK1c_000247
BPBio1_000632
AKOS016034302
ACon1_000139
IDI1_000247
MLS000069459
SMR000059108
NCGC00142617-01
NCGC00142617-03
MCULE-5348711723
NCGC00142617-02
EINECS 233-566-4
11032-31-8
17784-35-9
30174-44-8
30552-25-1
10236-47-2
10236-69-8
38664-96-9
109010-50-6
MolPort-001-742-592
Naringoside, Naringenine-7-rhamnosidoglucoside, 10236-47-2
Naringenin 7-O-alpha-L-rhamnosyl-(1->2)-beta-D-glucoside
Naringenin 7-O-[alpha-L-rhamnosyl-(1->2)-beta-D-glucoside]
naringenin 7-O-(alpha-L-rhamnosyl-(1,2)-beta-D-glucoside)
BRD-K02953697-002-03-3
5-Hydroxy-2-(4-hydroxyphenyl)-7-(2-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyloxy)-4-chromanon
7-(2-O-(6-Deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyloxy)-2,3-dihydro-4',5,7-trihydroxyflavone
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-betaD-glucopyranoside
(2S)-5-hydroxy-2-(4-hydroxyphenyl)-4-oxo-3,4-dihydro-2H-chromen-7-yl 2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside
4H-1-Benzopyran-4-one, 7-((2-O-(6-deoxy-alpha-L-mannapyranosyl)-beta-D-glucopyranosyl)oxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl), (S)-
4H-1-Benzopyran-4-one, 7-((2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (2S)-
(S)-7-((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydro-2H-pyran-2-yloxy)-tetrahydro-2H-pyran-2-yloxy)-5-hydroxy-2-(4-hydroxyphenyl)chroman-4-one
(S)-7-(((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-5-hydroxy-2-(4-hydroxyphenyl)chroman-4-one
(S)-7-(((2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-(((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-5-hydroxy-2-(4-hydroxyphenyl)
(2S)-7-{[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-{[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy}oxan-2-yl]oxy}-5-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one
7-[[2-O-(6-Deoxy-.alpha.-L-mannopyranosyl)-.beta.-D-glucopyranosyl]oxy]-5-hydroxy-2(S)-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
(2S)-7-[(2S,4S,5S,3R,6R)-3-((2S,6S,3R,4R,5R)-3,4,5-trihydroxy-6-methyl(2H-3,4, 5,6-tetrahydropyran-2-yloxy))-4,5-dihydroxy-6-(hydroxymethyl)(2H-3,4,5,6-tetra hydropyran-2-yloxy)]-5-hydroxy-2-(4-hydroxyphenyl)chroman-4-one
(2S)-7-[(2S,4S,5S,3R,6R)-3-((2S,6S,3R,4R,5R)-3,4,5-trihydroxy-6-methyl(2H-3,4, 5,6-tetrahydropyran-2-yloxy))-4,5-dihydroxy-6-(hydroxymethyl)(2H-3,4,5,6-tetra hydropyran-2-yloxy)]-5-hydroxy-2-(4-hydrox
(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chroman-4-one
(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one
(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-tetrahydropyran-2-yl]oxy-tetrahydropyran-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)chroman-4-one
Microorganism:

Yes

IUPAC name(2S)-7-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one
SMILESCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O
InchiInChI=1S/C27H32O14/c1-10-20(32)22(34)24(36)26(37-10)41-25-23(35)21(33)18(9-28)40-27(25)38-13-6-14(30)19-15(31)8-16(39-17(19)7-13)11-2-4-12(29)5-3-11/h2-7,10,16,18,20-30,32-36H,8-9H2,1H3/t10-,16-,18+,20-,21+,22+,23-,24+,25+,26-,27+/m0/s1
FormulaC27H32O14
PubChem ID442428
Molweight580.539
LogP-0.16
Atoms73
Bonds77
H-bond Acceptor14
H-bond Donor8
Chemical ClassificationFlavonoides alcohols benzenoids ethers

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAgaricus BisporusnaKoreaKim et al., 2008
FungiGanoderma LucidumnaKoreaKim et al., 2008
FungiInonotus ObliquusnaKoreaKim et al., 2008
FungiPleurotus EryngiinaKoreaKim et al., 2008
FungiPleurotus OstreatusnaKoreaKim et al., 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiAgaricus BisporusnaHPLCYes
FungiGanoderma LucidumnaHPLCYes
FungiInonotus ObliquusnaHPLCYes
FungiPleurotus EryngiinaHPLCYes
FungiPleurotus OstreatusnaHPLCYes