id | C00029788 |
---|---|
Name | Barbatic acid |
CAS RN | 17636-16-7 |
Standard InChI | InChI=1S/C19H20O7/c1-8-7-13(11(4)16(20)14(8)18(22)23)26-19(24)15-9(2)6-12(25-5)10(3)17(15)21/h6-7,20-21H,1-5H3,(H,22,23) |
Standard InChI (Main Layer) | InChI=1S/C19H20O7/c1-8-7-13(11(4)16(20)14(8)18(22)23)26-19(24)15-9(2)6-12(25-5)10(3)17(15)21/h6-7,20-21H,1-5H3,(H,22,23) |
Phytochemical cluster | |
---|---|
KCF-S cluster | No. 3861 |
By standard InChI | CHEMBL1902081 |
---|---|
By standard InChI Main Layer | CHEMBL1902081 |
By LinkDB |
---|
By CAS RN |
---|
class name | count |
---|
family name | count |
---|---|
Parmeliaceae | 1 |
Cladoniaceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Alectoria ochroleuca | 111641 | Parmeliaceae | Fungi | |
Cladonia rangiferina | 111670 | Cladoniaceae | Fungi |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
P37840 | Alpha-synuclein | Unclassified protein | CHEMBL1902081 |
CHEMBL2354282
(1)
|
4 / 2 |
P11473 | Vitamin D3 receptor | NR1I1 | CHEMBL1902081 |
CHEMBL1794311
(1)
|
2 / 3 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | CHEMBL1902081 |
CHEMBL1794584
(1)
|
2 / 0 |
O75496 | Geminin | Unclassified protein | CHEMBL1902081 |
CHEMBL2114843
(1)
|
0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | CHEMBL1902081 |
CHEMBL2114817
(1)
|
7 / 3 |
Q9UNA4 | DNA polymerase iota | Enzyme | CHEMBL1902081 |
CHEMBL1794483
(1)
|
0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#114500 | Colorectal cancer; crc |
P84022
|
#127750 | Dementia, lewy body; dlb |
P37840
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#174800 | Mccune-albright syndrome; mas |
P63092
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
#605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
#168600 | Parkinson disease, late-onset; pd |
P37840
|
#102200 | Pituitary adenoma, growth hormone-secreting |
P63092
|
#103580 | Pseudohypoparathyroidism, type ia; php1a |
P63092
|
#603233 | Pseudohypoparathyroidism, type ib; php1b |
P63092
|
#612462 | Pseudohypoparathyroidism, type ic; php1c |
P63092
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
KEGG | disease name | UniProt |
---|---|---|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H00057 | Parkinson's disease (PD) |
P37840
(related)
|
H00066 | Lewy body dementia (LBD) |
P37840
(related)
|
H00244 | Pseudohypoparathyroidism |
P63092
(related)
|
H00441 | Progressive osseous heteroplasia (POH) |
P63092
(related)
|
H00501 | Fibrous dysplasia, polyostotic |
P63092
(related)
|