id | C00009616 |
---|---|
Name | Pterocarpin / 3-Methoxy-8,9-methylenedioxypterocarpan |
CAS RN | 524-97-0 |
Standard InChI | InChI=1S/C17H14O5/c1-18-9-2-3-10-13(4-9)19-7-12-11-5-15-16(21-8-20-15)6-14(11)22-17(10)12/h2-6,12,17H,7-8H2,1H3 |
Standard InChI (Main Layer) | InChI=1S/C17H14O5/c1-18-9-2-3-10-13(4-9)19-7-12-11-5-15-16(21-8-20-15)6-14(11)22-17(10)12/h2-6,12,17H,7-8H2,1H3 |
Phytochemical cluster | No. 15 |
---|---|
KCF-S cluster | No. 66 |
By standard InChI | CHEMBL21103 |
---|---|
By standard InChI Main Layer | CHEMBL21103 CHEMBL242128 CHEMBL1983713 |
By LinkDB |
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By CAS RN |
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accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P13866 | Sodium/glucose cotransporter 1 | Glucose | CHEMBL242128 |
CHEMBL892510
(1)
|
1 / 1 |
P31639 | Sodium/glucose cotransporter 2 | Glucose | CHEMBL242128 |
CHEMBL892511
(1)
|
1 / 1 |
P28482 | Mitogen-activated protein kinase 1 | Erk | CHEMBL242128 |
CHEMBL1614521
(1)
|
0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | CHEMBL242128 |
CHEMBL1614421
(1)
CHEMBL1614502
(1)
|
4 / 3 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | CHEMBL242128 |
CHEMBL1614364
(1)
|
1 / 1 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | CHEMBL242128 |
CHEMBL1613933
(1)
|
0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | CHEMBL242128 |
CHEMBL1613933
(1)
|
1 / 6 |
OMIM | preferred title | UniProt |
---|---|---|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#606824 | Glucose/galactose malabsorption; ggm |
P13866
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#233100 | Renal glucosuria; glys1 |
P31639
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
KEGG | disease name | UniProt |
---|---|---|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H01261 | Congenital glucose-galactose malabsorption (GGM) |
P13866
(related)
|
H01126 | Familial renal glucosuria (FRG) |
P31639
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q9NUW8
(related)
|