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Substance
ID:1822742
Structure
Similarity
Functional Group
Text
ID:1738
trans-urocanic acid
Chemical Entities of Biological Interest
ID: CHEBI:30817
Names and Identifiers
IUPAC name
(2E)-3-(1H-imidazol-4-yl)prop-2-enoic acid
IUPAC Traditional name
urocanic acid
Synonyms
trans-urocanic acid
(2E)-3-(1H-imidazol-4-yl)acrylic acid
(E)-3-(1H-imidazol-4-yl)-2-propenoic acid
Urocanic acid
trans-urocanic acid
Registration numbers
Beilstein Number
81405
81403
CAS Number
104-98-3
3465-72-3
Wikipedia Title
Urocanic_acid
PubChem CID
736715
KEGG ID
C00785
PubMed Citation Links
9724745
Reaxys Registry
81403
ACToR Database
7699-35-6
BKMS React Database
30496
2876
149164
6622
BRENDA Database
3.5.1.68
4.1.1.22
4.3.1.3
1.14.17.3
4.2.1.49
1.3.99.33
BRENDA Ligand Database
2876
149164
6622
30496
CHEMBL
CHEMBL1236602
CompTox Database
DTXSID5041148
MetaboLights Database
MTBLS527
MTBLS440
MTBLS630
MTBLS670
MTBLS673
MTBLS926
MTBLS2295
MTBLS2274
MTBLS1693
MTBLS2394
MTBLS287
MTBLS2559
MTBLS138
MTBLS135
MTBLS1267
MTBLS1572
MTBLS159
MTBLS179
MTBLS204
MTBLS2081
MTBLS201
MTBLS3306
MTBLS406
MTBLS407
MTBLS1906
MTBLS220
Protein Data Bank
1uwk
1w1u
6t87
7ned
SABIO-RK Database
11319
1406
SureChEMBL Database
SCHEMBL15417
UniProt Database
Q556V9
Q5NZX8
A7ZAE4
C3P4M2
B1JV50
B9LLY0
Q7P188
B5XZ79
Q02ER8
Q5LRD8
Q1GSH0
A6TXF8
A2RGS5
P0DB75
B5XIY2
A1JSW6
Q8ZA10
Q664B8
C3L982
A0RH39
Q81Y45
A0K8U6
B4EDX5
Q0BDK6
A8AJ15
A6T6L1
Q1IRT8
Q9HU85
Q8VMR3
Q3KJE6
B5F069
A9MJE9
Q2FKP8
Q2G2P7
A3CL24
B7JI80
Q733H8
A9AGP7
Q891Q1
C1CWB4
Q5X5I5
Q88CZ7
Q57RG6
A5INP9
Q2YUR3
Q67JH4
B7ISJ2
C1EN93
B7HCD0
A3MLT7
Q9RZ06
A5IBM2
P21310
Q87UM1
B5FP58
Q5HJY8
A6QD47
P64415
Q9HLI6
Q8RBH4
Q8YD09
B7HKJ1
A7GR00
A2SA96
Q6AKP3
Q5ZVR0
Q1Q9E4
B5QX62
P64416
Q978N8
B9IUH0
Q81AC6
Q637H8
Q62LJ6
A3NXA3
Q54JI7
Q5WWW8
B9E7E0
A1STQ3
A5WDR1
B5R758
Q6GKT7
Q73Q56
Q9KBE6
Q6HFE9
A3NBH0
A4W8B5
Q0AP92
Q8XW29
B4TC45
B4SZJ4
Q6GD82
A8YYT1
Q9KSQ4
Q5WAZ6
P10944
Q5L310
Q11E18
Q5PG61
Q8NYY3
Q4A173
Q93TX3
Q5E0C6
A9VPT8
Q6G3U8
Q6FZP9
B2T2Y2
Q63SH6
C5D4K1
B8II08
P21213
A9MTJ1
C0PWX9
Q82I33
B5ETN1
Q8RFC2
A9IVW5
A7YWP4
Q39EP0
A4IK90
Q7NCB3
B0UQ15
P35492
Q1D6R1
Q983I0
B5BC34
Q9EWW1
Q87Q77
Q8RDU4
Q89GV3
A5EQB7
A4YNK7
A9H863
O31197
B4TQT6
A8AZ70
Q8DA21
A1TRE4
A5FZB9
B2SD96
Q2YIL6
A4JG46
Q20502
Q5FRR8
B2A3D9
A6WYU8
B6IWC6
Q8Z896
Q8ZQQ9
P24221
Q7MK58
Q9KWE4
B9JDC0
Q579E8
A9MCL0
B8H2S1
B0R544
A1AZX9
Q2RUU3
Q8EKJ4
P58083
Q8PLZ8
Q8U8Z7
B9K288
A5VVJ6
A9WVU3
P58082
B0SYU6
Q9HQD5
B4RED8
A3PK23
Q3J289
A8HA91
B8CGY5
P0DB74
Q4UTB9
A6TSX0
A8MF64
B8J950
Q8FVB4
A9WHT8
P42357
Q0BZK2
Q7N296
Q6LQ56
Q15X40
B9KSW6
A8G1S5
B1KP55
Q5X9K4
B0RUX3
Q2IIV4
B4UC43
B1YT80
Q1BHY5
Q5QV30
B7V3J1
Q162E2
A9GFW6
Q8NZ46
Q8PAA7
Q07W36
B0TM56
Q8EKJ5
A8HA92
A4Y1I2
A5F1X6
Q81Y46
B7JI79
Q733H9
B7ISJ1
Q86AX3
A4W8B4
P12381
P25080
B1J2Q5
Q87UM6
B8CGY4
A7MVK1
C1EN92
B7HCC9
B7HKJ0
A7HN21
Q5L084
Q9AGU4
Q4ZLW7
A0KRC6
A8G1S6
Q9KSQ3
C3LLP9
A7GQZ9
B9IUG9
C5DA19
Q2SEP6
B0R541
Q0HP37
Q0I0K5
Q87Q76
B7VMU2
Q81AC7
Q637H9
Q9HQD8
A9AW39
A1RQ57
B1KP56
Q8DA20
Q7MK59
Q9KBE5
Q6HFF0
Q96N76
Q0BZK0
Q5QV29
Q1GSG8
A5VFA2
P58987
Q3BV06
P58988
Q5WCP7
P25503
B5XZ80
A6T6L0
Q8XW28
Q983H8
Q5HDM6
A1JSW8
A7FP52
A9VPT7
Q6MJM2
C5C4W6
Q0AP94
Q11E20
B8II06
Q92V80
Q2RUU0
Q1AYH3
A4FNF1
Q931G1
P67417
Q1C0F6
B2K6P6
Q8ZA09
Q1CDD8
B7GUU5
B7I271
Q89GV4
Q8VC12
B5F068
A9MJF0
Q6GEA4
Q6G6Y9
B2I2C4
B0VPV2
A5EQB6
A0QRN3
B2A3D8
Q57RG7
B5FP57
P67418
Q49ZQ7
B0V9X6
A5FZC1
A4YNK8
B2SD94
A1SQ09
A6WYU6
B4REE0
B5QX61
Q82HL2
Q9KZ75
B1VUR5
B4SP57
B9JDB9
Q2YIL8
Q579F0
Q7N295
Q6LQ57
B5R757
B4TC44
B2FKG1
Q67JH5
Q8U8Z9
B9K286
A9MCL2
C0RM77
Q8YD12
A5VVJ8
Q48CE0
A6VDL7
B4SZJ3
A9MTJ2
C0PWX8
B4TQT5
B7IF30
B6ERX7
A9WVU5
Q8FVB2
Q9NAE2
B7V3J3
Q02ER6
Q9HU83
Q8Z897
B8E3L7
Q9HLI9
A6LP75
C1DJM5
A7ZAE5
B8H2R9
Q1I3Q8
C3K803
Q3IJC7
A3DAF4
A6WHI0
B0KCB9
Q8RCH9
A4TS44
Q664B7
B1JH60
C3P4M1
C3L983
Q9A9M1
B0SYU4
Q7P190
A5WA67
B0KM58
A9KV80
Q978N4
P53385
A0RH38
A8AJ16
Q9RZ02
Q88CZ6
Q8CVD0
HMDB Database
HMDB0034174
PDBeChem Database
URO
Golm Database
cf9f18ab-cc8d-49c7-908f-0fe265e9f567
c0d3fc9c-1f06-40b4-90d9-b1df046bc0ef
Patent number
RU2445307
DrugBank ID
DB01971
Reactom Database
R-HSA-70899
R-HSA-70903
CHEBI ID
CHEBI:30817
CHEBI:46392
CHEBI:9899
PubChem SID
8145216
Properties
No Data Available
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Molecule Details
A urocanic acid in which the double bond of the carboxyethene moiety has E configuration.
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