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Substance
ID:1833101
Structure
Similarity
Functional Group
Text
ID:1894
7H-xanthine
Chemical Entities of Biological Interest
ID: CHEBI:48517
Names and Identifiers
IUPAC name
2,3,6,7-tetrahydro-1H-purine-2,6-dione
IUPAC Traditional name
xanthine
Synonyms
Xanthine
7H-xanthine
Registration numbers
Beilstein Number
8733
CAS Number
69-89-6
PubChem CID
1188
KEGG ID
C00385
PubMed Citation Links
22770225
ACToR Database
16819-86-6
CHEMBL
CHEMBL1424
CompTox Database
DTXSID4035120
Protein Data Bank
1a96
1yr3
2uz9
2w3s
3eub
3gao
3l8w
3odg
5grk
5h9i
5i6c
5ruy
6oha
7elp
7elq
7elr
SABIO-RK Database
194
7776
16172
3547
6745
6764
6721
10986
196
197
323
12908
192
127
SureChEMBL Database
SCHEMBL4965
UniProt Database
Q46509
P18892
Q13410
Q62556
A1A4Q9
Q96DE0
Q6P3D0
Q2V8X7
Q6TEC1
P20035
P07833
Q26997
P51900
Q4WV19
A4RPM5
A2R3H4
Q2TWN3
A1DED8
Q0CFD4
A7F582
Q46821
Q07307
A1CAZ7
O59954
B0Y0P7
D7REY3
O32146
Q8X6C7
Q46799
Q8X6C5
O32145
O32144
Q46814
O32143
P80457
P08793
P47990
Q54FB7
P10351
P22811
P91711
Q12553
F4JLI5
Q46800
Q8X6C4
Q46801
Q8XD64
P0AGN0
Q8GUQ8
O32147
P0AGN1
P0AGM9
P0AGN2
P67446
P67445
P67444
O34598
Q9RYX4
Q86AW9
P76641
Q9Y2T3
Q9R111
Q5RAV9
Q9WTT6
O14057
Q07729
Q41760
O33819
Q4QMM6
A3MYX7
Q72D63
A1VES8
P0A9M5
B7N8G9
B6I018
Q65QN6
Q11IP4
A6VKR2
A7ZHZ7
B1LHT4
Q9MYW6
A0KNR2
A4SJF2
B7UJC6
B7MC88
Q1RFT3
Q1QK75
P47989
Q8UEM6
B7L3Z0
C5B9M4
Q3SQJ9
B6EIE9
P0A9M6
A4W6X0
A6X0U5
Q00519
Q89IM4
B5Z1I2
B2VHN3
Q9CL73
Q2YQ27
A9MB59
B7NK87
B7LNG2
Q5FUI1
Q6AUV1
Q8YH64
B7MQ74
Q7VKP2
P22985
B0CGJ6
Q8G0P3
B7M267
P43859
P57339
C4ZT95
B1XDY1
Q0I1C0
Q8K9R8
A7ZWK1
B0UWV5
Q89AN2
Q1QVR0
A1A7U9
Q5QW45
A8AKQ0
Q0TL78
Q28PG8
A7MEN2
Q8FKM7
B5Y1E0
Q311U1
B1J0Z6
Q4QMP2
Q6AQG4
A6T532
A4WRD6
Q163Y8
Q5LRI5
Q325P8
Q32J21
Q1CLD0
A4TPK4
Q1GHI7
Q0T7Q9
Q66DZ2
B5EWK0
P0A9M7
B1JIH6
Q6D1I0
A9MNR9
Q57ST7
Q3Z599
A6U9A2
C6DCY0
B5FJW9
Q2NVF2
Q7N7B4
Q6LTX6
B5R4S1
A5F5Y8
B4EUU7
B5R5R4
A7MWU9
Q9KPT5
Q2K9D7
B4T7Q0
B4SVV9
C3LQ49
Q1MHW9
Q5PF80
Q5E6W3
Q87RV3
Q98NH3
Q92PU1
A9MY09
B7VJB5
Q2IV51
C0Q6T6
Q8DF90
Q7MN62
Q6N7S7
B5BDQ2
B4TZ85
A1JNY0
Q212I9
P0A278
A7FLI5
Q1C4E3
Q138L1
A3PIG2
P0A277
B2K658
Q3J3Y6
A8GAD0
Q8ZC05
A9R2X4
B2U3S9
B1YHS1
C4L0T7
Q046I4
A8YXG4
Q0TUB1
Q8XNJ8
A5I0Y0
A7GCI1
B7GW49
B7I9E1
A7GNB6
B9IVT8
B2TL11
B8I1G1
Q74LF9
Q185K4
B0S259
Q0SW58
Q0TQZ9
B2HZ61
B7IPE6
C1ENK3
Q81FL2
A0Q2P2
A4IN63
Q9CGF0
A1A190
B3DSF5
B0TCJ8
A2RKX0
A9KTA4
Q02Z29
Q8XKV0
A3M938
A6TTD6
B7JHT4
B7HHX2
Q63DG7
Q8G5W1
Q891I6
Q65I86
Q5FMD9
A8FEE7
B7GSB6
C1CZX7
Q03Q10
Q88XQ4
A7FPI7
Q0STE8
Q73AS5
Q5LEQ1
C0ZJ16
Q03A64
A5VLG9
C1DJZ2
P42085
Q8AAN7
Q1J141
A5HYL0
A7Z5W2
B7HL82
Q64VN7
Q5WI27
A9WA88
Q9RTY2
B3WDB0
B2G8U2
C3P5T8
A6L3C5
B9LCT9
A4J6I7
Q1GBU9
Q1WSL3
A7GA73
C3L8M1
Q9KCQ5
Q97KP4
Q831Y0
Q04CA6
Q38VB9
P47165
A7FT29
Q6F7W2
A9VMH5
B2GDT2
A0RC17
A6LW55
C4ZA66
Q81SQ5
Q6HKZ0
B2V327
B8DUR4
Q9ZPR7
Q7MT44
Q48QC3
Q7CN84
A4VGU2
A7WY89
Q5HRX4
Q8CQR0
Q1JBS4
B9DS40
A6VEA3
A6TYN9
Q4L383
Q1JLQ7
C1CG72
C1DBA1
Q03UJ4
B7V5I9
Q2FJM8
Q49UU6
Q1JGV7
C1CMF7
C1CT78
Q92AC4
Q02E64
Q2G0Y9
Q3K111
Q1J6M6
C1KWI4
Q9HTQ6
A5IPW7
Q8E5B5
A2REI4
Q71YD1
Q1I2W1
Q2YVL8
Q8DZL5
B1I857
Q8Y617
Q4K3U3
Q5HIQ9
C0MBC1
B8ZN87
A0AJZ0
C3K452
A8AXD5
Q48TL5
B9E8Y3
A4XNV9
A6QE68
Q99WJ1
Q9ZEE3
Q97P00
Q2RKK1
A5WAY3
Q7A7I5
Q99ZQ0
P0DH49
Q8CUP6
Q3K4P7
Q04IV9
B2ISU6
Q04GD7
B0KQ69
Q6GJQ9
Q6GC84
P0DH48
B5XLI3
A6LC43
Q88CB6
A8Z0Q8
B5E1V8
Q8DNL1
Q03EG0
Q88BA5
Q7A1T6
Q5XC74
C0MF03
B2RH69
Q500M2
B9DM01
C1C9B2
A3CMY9
Q9AGS1
Q5FB27
G3X982
O54754
Q5QE80
H9TB18
P80456
Q3TYQ9
Q5QE79
P48034
Q9Z0U5
H9TB19
C4NYZ3
H9TB17
Q5SGK3
Q06278
Q5QE78
P82858
Q8X6J4
P77489
Q8X6J0
P77324
Q8X6I9
P77165
P42086
Q4J6M3
Q0QLF2
Q0QLF1
Q7G9P4
Q852M2
Q7G191
Q6Z351
Q69R21
Q7G193
O23887
Q7XH05
Q7G192
O23888
Q852M1
Q7SEW2
A7EVF4
B0XYQ4
B0WSW8
Q4WWW9
Q0V5W8
A2QF55
B2WKU1
Q16P87
B0WSX1
Q0V713
Q16P90
Q7QFL7
Q9C5X8
Q9Y8C2
A6R104
Q2U4W2
B2WBW4
Q9Y8C1
Q1DQS9
Q2KF83
A2QYG2
Q16GH0
A1CJM9
A1D7X4
Q96EN8
A8X493
B4H0S8
A4RK48
A2QIK9
B4JXP7
Q21657
Q29GM0
Q14CH1
Q2UH11
Q9VRA2
Q2HE65
B4M3C9
A1CX75
Q0CLW8
B4L340
Q5RKZ7
A2VD33
B4N1V2
Q7SE17
Q8IU29
Q559G8
B4PYH5
Q655R6
A1CHL0
A6SRX6
Q9UV64
Q8LGM7
B0Y691
B3MZN7
Q9N0E7
Q4WPE6
B3NY19
HMDB Database
HMDB0000292
PDBeChem Database
XAN
VirtualMetabolicHuman Database
xan
NMRShiftDB Database
20191749
BindingDB Database
82009
50227193
BPDB Database
2,153
KNApSAcK Database
C00019660
MetaCyc Database
XANTHINE
Reaxys Registry
8733
BRENDA Database
3.5.4.3
5.6.1.6
6.3.4.2
2.3.1.1
4.4.1.5
3.1.2.6
1.4.1.14
1.7.3.3
1.17.3.1
2.4.2.1
2.4.2.22
2.4.2.7
2.4.2.8
2.4.2.4
2.5.1.6
2.4.2.16
1.17.1.4
1.17.3.2
2.4.2.64
1.14.11.48
1.2.3.1
3.2.2.21
3.2.2.28
1.14.13.128
1.14.13.179
3.2.2.2
3.2.2.8
3.2.2.1
3.5.4.2
3.5.4.4
3.5.4.32
3.2.2.3
1.14.13.178
3.2.2.15
3.2.2.27
2.4.2.20
2.4.2.6
2.4.2.5
MetaboLights Database
MTBLS816
MTBLS106
MTBLS1040
MTBLS136
MTBLS2274
Wikipedia Title
Xanthine
Patent number
EP1669074
EnzymePortal Database
P82858
DrugBank ID
DB02134
Gmelin ID
142613
CHEBI ID
CHEBI:48517
PubChem SID
49658808
Properties
No Data Available
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Molecule Details
An oxopurine in which the purine ring is substituted by oxo groups at positions 2 and 6 and N-7 is protonated.
Molecular Spectra
No Data Available
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References
No Data Available
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Names and Identifiers
Registration numbers
Properties
Molecule Details
Molecular Spectra
References