Substance

ID:1833101

Names and Identifiers
IUPAC name
2,3,6,7-tetrahydro-1H-purine-2,6-dione
IUPAC Traditional name
xanthine
Synonyms
Xanthine7H-xanthine
Registration numbers
Beilstein Number
CAS Number
PubChem CID
KEGG ID
PubMed Citation Links
ACToR Database
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UniProt Database
Q46509P18892Q13410Q62556A1A4Q9Q96DE0Q6P3D0Q2V8X7Q6TEC1P20035P07833Q26997P51900Q4WV19A4RPM5A2R3H4Q2TWN3A1DED8Q0CFD4A7F582Q46821Q07307A1CAZ7O59954B0Y0P7D7REY3O32146Q8X6C7Q46799Q8X6C5O32145O32144Q46814O32143P80457P08793P47990Q54FB7P10351P22811P91711Q12553F4JLI5Q46800Q8X6C4Q46801Q8XD64P0AGN0Q8GUQ8O32147P0AGN1P0AGM9P0AGN2P67446P67445P67444O34598Q9RYX4Q86AW9P76641Q9Y2T3Q9R111Q5RAV9Q9WTT6O14057Q07729Q41760O33819Q4QMM6A3MYX7Q72D63A1VES8P0A9M5B7N8G9B6I018Q65QN6Q11IP4A6VKR2A7ZHZ7B1LHT4Q9MYW6A0KNR2A4SJF2B7UJC6B7MC88Q1RFT3Q1QK75P47989Q8UEM6B7L3Z0C5B9M4Q3SQJ9B6EIE9P0A9M6A4W6X0A6X0U5Q00519Q89IM4B5Z1I2B2VHN3Q9CL73Q2YQ27A9MB59B7NK87B7LNG2Q5FUI1Q6AUV1Q8YH64B7MQ74Q7VKP2P22985B0CGJ6Q8G0P3B7M267P43859P57339C4ZT95B1XDY1Q0I1C0Q8K9R8A7ZWK1B0UWV5Q89AN2Q1QVR0A1A7U9Q5QW45A8AKQ0Q0TL78Q28PG8A7MEN2Q8FKM7B5Y1E0Q311U1B1J0Z6Q4QMP2Q6AQG4A6T532A4WRD6Q163Y8Q5LRI5Q325P8Q32J21Q1CLD0A4TPK4Q1GHI7Q0T7Q9Q66DZ2B5EWK0P0A9M7B1JIH6Q6D1I0A9MNR9Q57ST7Q3Z599A6U9A2C6DCY0B5FJW9Q2NVF2Q7N7B4Q6LTX6B5R4S1A5F5Y8B4EUU7B5R5R4A7MWU9Q9KPT5Q2K9D7B4T7Q0B4SVV9C3LQ49Q1MHW9Q5PF80Q5E6W3Q87RV3Q98NH3Q92PU1A9MY09B7VJB5Q2IV51C0Q6T6Q8DF90Q7MN62Q6N7S7B5BDQ2B4TZ85A1JNY0Q212I9P0A278A7FLI5Q1C4E3Q138L1A3PIG2P0A277B2K658Q3J3Y6A8GAD0Q8ZC05A9R2X4B2U3S9B1YHS1C4L0T7Q046I4A8YXG4Q0TUB1Q8XNJ8A5I0Y0A7GCI1B7GW49B7I9E1A7GNB6B9IVT8B2TL11B8I1G1Q74LF9Q185K4B0S259Q0SW58Q0TQZ9B2HZ61B7IPE6C1ENK3Q81FL2A0Q2P2A4IN63Q9CGF0A1A190B3DSF5B0TCJ8A2RKX0A9KTA4Q02Z29Q8XKV0A3M938A6TTD6B7JHT4B7HHX2Q63DG7Q8G5W1Q891I6Q65I86Q5FMD9A8FEE7B7GSB6C1CZX7Q03Q10Q88XQ4A7FPI7Q0STE8Q73AS5Q5LEQ1C0ZJ16Q03A64A5VLG9C1DJZ2P42085Q8AAN7Q1J141A5HYL0A7Z5W2B7HL82Q64VN7Q5WI27A9WA88Q9RTY2B3WDB0B2G8U2C3P5T8A6L3C5B9LCT9A4J6I7Q1GBU9Q1WSL3A7GA73C3L8M1Q9KCQ5Q97KP4Q831Y0Q04CA6Q38VB9P47165A7FT29Q6F7W2A9VMH5B2GDT2A0RC17A6LW55C4ZA66Q81SQ5Q6HKZ0B2V327B8DUR4Q9ZPR7Q7MT44Q48QC3Q7CN84A4VGU2A7WY89Q5HRX4Q8CQR0Q1JBS4B9DS40A6VEA3A6TYN9Q4L383Q1JLQ7C1CG72C1DBA1Q03UJ4B7V5I9Q2FJM8Q49UU6Q1JGV7C1CMF7C1CT78Q92AC4Q02E64Q2G0Y9Q3K111Q1J6M6C1KWI4Q9HTQ6A5IPW7Q8E5B5A2REI4Q71YD1Q1I2W1Q2YVL8Q8DZL5B1I857Q8Y617Q4K3U3Q5HIQ9C0MBC1B8ZN87A0AJZ0C3K452A8AXD5Q48TL5B9E8Y3A4XNV9A6QE68Q99WJ1Q9ZEE3Q97P00Q2RKK1A5WAY3Q7A7I5Q99ZQ0P0DH49Q8CUP6Q3K4P7Q04IV9B2ISU6Q04GD7B0KQ69Q6GJQ9Q6GC84P0DH48B5XLI3A6LC43Q88CB6A8Z0Q8B5E1V8Q8DNL1Q03EG0Q88BA5Q7A1T6Q5XC74C0MF03B2RH69Q500M2B9DM01C1C9B2A3CMY9Q9AGS1Q5FB27G3X982O54754Q5QE80H9TB18P80456Q3TYQ9Q5QE79P48034Q9Z0U5H9TB19C4NYZ3H9TB17Q5SGK3Q06278Q5QE78P82858Q8X6J4P77489Q8X6J0P77324Q8X6I9P77165P42086Q4J6M3Q0QLF2Q0QLF1Q7G9P4Q852M2Q7G191Q6Z351Q69R21Q7G193O23887Q7XH05Q7G192O23888Q852M1Q7SEW2A7EVF4B0XYQ4B0WSW8Q4WWW9Q0V5W8A2QF55B2WKU1Q16P87B0WSX1Q0V713Q16P90Q7QFL7Q9C5X8Q9Y8C2A6R104Q2U4W2B2WBW4Q9Y8C1Q1DQS9Q2KF83A2QYG2Q16GH0A1CJM9A1D7X4Q96EN8A8X493B4H0S8A4RK48A2QIK9B4JXP7Q21657Q29GM0Q14CH1Q2UH11Q9VRA2Q2HE65B4M3C9A1CX75Q0CLW8B4L340Q5RKZ7A2VD33B4N1V2Q7SE17Q8IU29Q559G8B4PYH5Q655R6A1CHL0A6SRX6Q9UV64Q8LGM7B0Y691B3MZN7Q9N0E7Q4WPE6B3NY19
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Wikipedia Title
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EnzymePortal Database
DrugBank ID
Gmelin ID
CHEBI ID
PubChem SID
Properties
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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
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