| id | C00002503 |
|---|---|
| Name | Umbelliferon / Umbelliferone / 7-Hydroxycoumarin |
| CAS RN | 93-35-6 |
| Standard InChI | InChI=1S/C9H6O3/c10-7-3-1-6-2-4-9(11)12-8(6)5-7/h1-5,10H |
| Standard InChI (Main Layer) | InChI=1S/C9H6O3/c10-7-3-1-6-2-4-9(11)12-8(6)5-7/h1-5,10H |
| Phytochemical cluster | No. 25 |
|---|---|
| KCF-S cluster | No. 1030 |
| By standard InChI | CHEMBL51628 |
|---|---|
| By standard InChI Main Layer | CHEMBL51628 |
| By LinkDB | C09315 |
|---|
| By CAS RN | C031477 |
|---|
| class name | count |
|---|---|
| rosids | 40 |
| asterids | 29 |
| eudicotyledons | 2 |
| Spermatophyta | 1 |
| family name | count |
|---|---|
| Apiaceae | 19 |
| Rutaceae | 15 |
| Fabaceae | 11 |
| Moraceae | 5 |
| Thymelaeaceae | 4 |
| Hydrangeaceae | 4 |
| Asteraceae | 4 |
| Picramniaceae | 3 |
| Solanaceae | 2 |
| Biebersteiniaceae | 1 |
| accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|---|
| P22310 | UDP-glucuronosyltransferase 1-4 | Enzyme | CHEMBL51628 |
CHEMBL1908081
(1)
CHEMBL1908082
(1)
|
3 / 0 |
| Q9HAW8 | UDP-glucuronosyltransferase 1-10 | Enzyme | CHEMBL51628 |
CHEMBL1908087
(2)
|
0 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | CHEMBL51628 |
CHEMBL2114784
(1)
|
1 / 1 |
| P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | CHEMBL51628 |
CHEMBL1014033
(1)
|
0 / 3 |
| P04062 | Glucosylceramidase | Enzyme | CHEMBL51628 |
CHEMBL1613818
(1)
|
6 / 4 |
| P10253 | Lysosomal alpha-glucosidase | Hydrolase | CHEMBL51628 |
CHEMBL1614175
(1)
|
1 / 1 |
| P29466 | Caspase-1 | C14 | CHEMBL51628 |
CHEMBL1614158
(1)
|
0 / 0 |
| P04406 | Glyceraldehyde-3-phosphate dehydrogenase | Enzyme | CHEMBL51628 |
CHEMBL684062
(1)
|
0 / 0 |
| P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | CHEMBL51628 |
CHEMBL892636
(1)
|
1 / 1 |
| P00918 | Carbonic anhydrase 2 | Lyase | CHEMBL51628 |
CHEMBL1212359
(1)
CHEMBL1290838
(1)
CHEMBL1941822 (1) |
1 / 2 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL51628 |
CHEMBL1614458
(1)
|
0 / 0 |
| P28845 | Corticosteroid 11-beta-dehydrogenase isozyme 1 | Enzyme | CHEMBL51628 |
CHEMBL1656573
(1)
CHEMBL1656574
(1)
|
1 / 1 |
| O43570 | Carbonic anhydrase 12 | Lyase | CHEMBL51628 |
CHEMBL1212361
(1)
CHEMBL1941824
(1)
|
1 / 2 |
| P39748 | Flap endonuclease 1 | Enzyme | CHEMBL51628 |
CHEMBL1794486
(1)
|
0 / 0 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | CHEMBL51628 |
CHEMBL1738606
(1)
|
0 / 0 |
| O75496 | Geminin | Unclassified protein | CHEMBL51628 |
CHEMBL2114843
(1)
|
0 / 0 |
| P54855 | UDP-glucuronosyltransferase 2B15 | Enzyme | CHEMBL51628 |
CHEMBL1908090
(1)
|
0 / 0 |
| P18405 | 3-oxo-5-alpha-steroid 4-dehydrogenase 1 | Oxidoreductase | CHEMBL51628 |
CHEMBL816490
(1)
|
0 / 0 |
| P15121 | Aldose reductase | Enzyme | CHEMBL51628 |
CHEMBL1260797
(1)
|
0 / 0 |
| P00915 | Carbonic anhydrase 1 | Lyase | CHEMBL51628 |
CHEMBL1212358
(1)
CHEMBL1290837
(1)
CHEMBL1941821 (1) |
0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | CHEMBL51628 |
CHEMBL1794401
(1)
|
0 / 0 |
| P14679 | Tyrosinase | Oxidoreductase | CHEMBL51628 |
CHEMBL1780390
(1)
|
4 / 2 |
| P06280 | Alpha-galactosidase A | Enzyme | CHEMBL51628 |
CHEMBL1614217
(1)
CHEMBL1614369
(1)
|
1 / 1 |
| P56817 | Beta-secretase 1 | A1A | CHEMBL51628 |
CHEMBL1936881
(1)
CHEMBL1936882
(1)
|
0 / 0 |
| Q16790 | Carbonic anhydrase 9 | Lyase | CHEMBL51628 |
CHEMBL1212360
(1)
CHEMBL1290839
(1)
CHEMBL1941823 (1) |
0 / 1 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | CHEMBL51628 |
CHEMBL1613910
(1)
|
3 / 3 |
| P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | CHEMBL51628 |
CHEMBL1614038
(1)
|
2 / 2 |
| Q9HAW9 | UDP-glucuronosyltransferase 1-8 | Enzyme | CHEMBL51628 |
CHEMBL1908085
(2)
|
0 / 0 |
| Q9Y4X1 | UDP-glucuronosyltransferase 2A1 | Enzyme | CHEMBL51628 |
CHEMBL1908088
(1)
|
0 / 0 |
| P22303 | Acetylcholinesterase | Hydrolase | CHEMBL51628 |
CHEMBL1003053
(1)
|
1 / 0 |
| Q00796 | Sorbitol dehydrogenase | Enzyme | CHEMBL51628 |
CHEMBL1260799
(1)
|
0 / 0 |
| P55210 | Caspase-7 | C14 | CHEMBL51628 |
CHEMBL1613779
(1)
|
0 / 0 |
| P22309 | UDP-glucuronosyltransferase 1-1 | Enzyme | CHEMBL51628 |
CHEMBL1908080
(1)
|
5 / 1 |
| P80365 | Corticosteroid 11-beta-dehydrogenase isozyme 2 | Enzyme | CHEMBL51628 |
CHEMBL1656575
(1)
CHEMBL1656576
(1)
|
1 / 1 |
| B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL51628 |
CHEMBL1613914
(1)
|
0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | CHEMBL51628 |
CHEMBL1614364
(1)
|
1 / 1 |
| O00255 | Menin | Unclassified protein | CHEMBL51628 |
CHEMBL1614531
(1)
|
2 / 5 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | CHEMBL51628 |
CHEMBL1614531
(1)
|
1 / 3 |
| O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | CHEMBL51628 |
CHEMBL2114738
(1)
|
0 / 0 |
| compound | gene | gene name | gene description | interaction | interaction type | form |
reference
pmid |
|---|---|---|---|---|---|---|---|
| C031477 | 8644 |
AKR1C3
DD3 DDX HA1753 HAKRB HAKRe HSD17B5 PGFS hluPGFS |
aldo-keto reductase family 1, member C3 (EC:1.3.1.20 1.1.1.188 1.1.1.239 1.1.1.64 1.1.1.112 1.1.1.357) | 7-hydroxycoumarin inhibits the reaction [AKR1C3 mutant form results in increased susceptibility to 4-hydroxy-2-nonenal] |
decreases reaction
/ increases response to substance |
mutant form |
22964423
|
| C031477 | 8644 |
AKR1C3
DD3 DDX HA1753 HAKRB HAKRe HSD17B5 PGFS hluPGFS |
aldo-keto reductase family 1, member C3 (EC:1.3.1.20 1.1.1.188 1.1.1.239 1.1.1.64 1.1.1.112 1.1.1.357) | 7-hydroxycoumarin inhibits the reaction [AKR1C3 mutant form results in increased susceptibility to Hydrogen Peroxide] |
decreases reaction
/ increases response to substance |
mutant form |
22964423
|
| C031477 | 8644 |
AKR1C3
DD3 DDX HA1753 HAKRB HAKRe HSD17B5 PGFS hluPGFS |
aldo-keto reductase family 1, member C3 (EC:1.3.1.20 1.1.1.188 1.1.1.239 1.1.1.64 1.1.1.112 1.1.1.357) | 7-hydroxycoumarin results in increased expression of AKR1C3 protein |
increases expression
|
protein |
22964423
|
| C031477 | 8574 |
AKR7A2
AFAR AFAR1 AFB1-AR1 AKR7 |
aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) (EC:1.1.1.n11) | 7-hydroxycoumarin affects the reaction [AKR7A2 mutant form results in increased susceptibility to 4-hydroxy-2-nonenal] |
affects reaction
/ increases response to substance |
mutant form |
22964423
|
| C031477 | 8574 |
AKR7A2
AFAR AFAR1 AFB1-AR1 AKR7 |
aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) (EC:1.1.1.n11) | 7-hydroxycoumarin results in increased expression of AKR7A2 protein |
increases expression
|
protein |
22964423
|
| C031477 | 581 |
BAX
BCL2L4 |
BCL2-associated X protein | 7-hydroxycoumarin results in increased expression of BAX protein |
increases expression
|
protein |
15964220
|
| C031477 | 596 |
BCL2
Bcl-2 PPP1R50 |
B-cell CLL/lymphoma 2 | 7-hydroxycoumarin results in decreased expression of BCL2 protein |
decreases expression
|
protein |
15964220
|
| C031477 | 595 |
CCND1
BCL1 D11S287E PRAD1 U21B31 |
cyclin D1 | 7-hydroxycoumarin results in decreased expression of CCND1 protein |
decreases expression
|
protein |
11679177
|
| C031477 | 1548 |
CYP2A6
CPA6 CYP2A CYP2A3 CYPIIA6 P450C2A P450PB |
cytochrome P450, family 2, subfamily A, polypeptide 6 (EC:1.14.14.1) | CYP2A6 protein results in increased chemical synthesis of 7-hydroxycoumarin |
increases chemical synthesis
|
protein |
11376561
11393269 11927840 12401345 15155557 |
| C031477 | 6817 |
SULT1A1
HAST1/HAST2 P-PST PST ST1A1 ST1A3 STP STP1 TSPST1 |
sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (EC:2.8.2.1) | SULT1A1 protein results in increased sulfation of 7-hydroxycoumarin |
increases sulfation
|
protein |
11181495
|
| C031477 | 54600 |
UGT1A9
HLUGP4 LUGP4 UDPGT UDPGT_1-9 UGT-1I UGT1-09 UGT1-9 UGT1.9 UGT1AI UGT1I |
UDP glucuronosyltransferase 1 family, polypeptide A9 (EC:2.4.1.17) | UGT1A9 protein results in increased glucuronidation of 7-hydroxycoumarin |
increases glucuronidation
|
protein |
15044611
|
| C031477 | 7366 |
UGT2B15
HLUG4 UDPGT_2B8 UDPGT2B15 UDPGTH3 UGT2B8 |
UDP glucuronosyltransferase 2 family, polypeptide B15 (EC:2.4.1.17) | UGT2B15 protein results in increased metabolism of 7-hydroxycoumarin |
increases metabolic processing
|
protein |
7835232
|
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
| #203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
| #606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
| #218030 | Apparent mineralocorticoid excess; ame |
P80365
|
| #601816 | Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 |
P22309
|
| #604931 | Cortisone reductase deficiency 1; cortrd1 |
P28845
|
| #218800 | Crigler-najjar syndrome, type i |
P22309
P22310 |
| #606785 | Crigler-najjar syndrome, type ii |
P22309
P22310 |
| #119900 | Digital clubbing, isolated congenital |
P15428
|
| #301500 | Fabry disease |
P06280
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #143500 | Gilbert syndrome |
P22309
P22310 |
| #232300 | Glycogen storage disease ii |
P10253
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #237900 | Hyperbilirubinemia, transient familial neonatal; hblrtfn |
P22309
|
| #143860 | Hyperchlorhidrosis, isolated |
O43570
|
| #145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
| #259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
| #259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| #601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #278300 | Xanthinuria, type i |
P47989
|
| #112100 | Yt blood group antigen |
P22303
|
| KEGG | disease name | UniProt |
|---|---|---|
| H00033 | Adrenal carcinoma |
O00255
(related)
|
| H00034 | Carcinoid |
O00255
(related)
|
| H00045 | Malignant islet cell carcinoma |
O00255
(related)
|
| H00246 | Primary hyperparathyroidism |
O00255
(related)
|
| H01102 | Pituitary adenomas |
O00255
(related)
|
| H01302 | Hyperchlorhidrosis isolated (HCHLH) |
O43570
(related)
|
| H00021 | Renal cell carcinoma |
O43570
(marker)
Q16790 (marker) |
| H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
| H00436 | Osteopetrosis |
P00918
(related)
|
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00125 | Fabry disease |
P06280
(related)
|
| H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
| H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
| H00038 | Malignant melanoma |
P14679
(marker)
|
| H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
| H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
| H00208 | Hyperbilirubinemia |
P22309
(related)
|
| H01111 | Cortisone reductase deficiency (CRD) |
P28845
(related)
|
| H00017 | Esophageal cancer |
P35354
(related)
|
| H00025 | Penile cancer |
P35354
(related)
|
| H00046 | Cholangiocarcinoma |
P35354
(related)
|
| H00192 | Xanthinuria |
P47989
(related)
|
| H00259 | Apparent mineralocorticoid excess syndrome |
P80365
(related)
|
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
| H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
| H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|