id | C00017751 |
---|---|
Name | MH 435A / Erbstatin / Antibiotic MH 435A |
CAS RN | 100827-28-9 |
Standard InChI | InChI=1S/C9H9NO3/c11-6-10-4-3-7-5-8(12)1-2-9(7)13/h1-6,12-13H,(H,10,11)/b4-3+ |
Standard InChI (Main Layer) | InChI=1S/C9H9NO3/c11-6-10-4-3-7-5-8(12)1-2-9(7)13/h1-6,12-13H,(H,10,11) |
Phytochemical cluster | No. 6 |
---|---|
KCF-S cluster | No. 3417 |
By standard InChI | CHEMBL47986 |
---|---|
By standard InChI Main Layer | CHEMBL47986 CHEMBL2001273 |
By LinkDB |
---|
By CAS RN | C048212 |
---|
class name | count |
---|
family name | count |
---|---|
Streptomycetaceae | 1 |
KNApSAcK organism | *ID | *family | *plant class | *kingdom |
---|---|---|---|---|
Streptomyces No. NH435-hF3 | 1883 | Streptomycetaceae | Bacteria |
accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|---|
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | CHEMBL47986 |
CHEMBL1738312
(1)
|
0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | CHEMBL47986 |
CHEMBL2114784
(1)
|
1 / 1 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | CHEMBL47986 |
CHEMBL1794499
(1)
|
2 / 0 |
P14618 | Pyruvate kinase PKM | Enzyme | CHEMBL47986 |
CHEMBL1613996
(1)
CHEMBL1614428
(1)
|
0 / 0 |
P06746 | DNA polymerase beta | Enzyme | CHEMBL47986 |
CHEMBL1614079
(1)
|
0 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | CHEMBL47986 |
CHEMBL1614076
(1)
|
1 / 1 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | CHEMBL47986 |
CHEMBL1794585
(1)
|
0 / 0 |
P00533 | Epidermal growth factor receptor | TK tyrosine-protein kinase EGFR subfamily | CHEMBL47986 |
CHEMBL674029
(1)
CHEMBL674643
(1)
CHEMBL674699 (1) CHEMBL674706 (1) CHEMBL1012122 (1) CHEMBL941412 (1) |
1 / 11 |
P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL47986 |
CHEMBL1614458
(1)
|
0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | CHEMBL47986 |
CHEMBL1794486
(1)
|
0 / 0 |
O75496 | Geminin | Unclassified protein | CHEMBL47986 |
CHEMBL2114843
(1)
CHEMBL2114780
(1)
|
0 / 0 |
P07711 | Cathepsin L1 | C1A | CHEMBL47986 |
CHEMBL1614088
(1)
|
0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | CHEMBL47986 |
CHEMBL1794569
(1)
|
1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | CHEMBL47986 |
CHEMBL1614280
(1)
|
0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | CHEMBL47986 |
CHEMBL1794401
(1)
|
0 / 0 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | CHEMBL47986 |
CHEMBL1963863
(1)
|
0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | CHEMBL47986 |
CHEMBL1794483
(1)
|
0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | CHEMBL47986 |
CHEMBL1737991
(1)
|
0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | CHEMBL47986 |
CHEMBL1614211
(1)
|
0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | CHEMBL47986 |
CHEMBL1614250
(1)
CHEMBL1614421
(1)
CHEMBL1614502 (1) |
4 / 3 |
Q9GZV3 | High affinity choline transporter 1 | Choline Na-symporter | CHEMBL47986 |
CHEMBL1794362
(1)
CHEMBL1794546
(1)
|
1 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | CHEMBL47986 |
CHEMBL1794536
(1)
|
0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | CHEMBL47986 |
CHEMBL1613914
(1)
|
0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | CHEMBL47986 |
CHEMBL1738442
(1)
|
0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | CHEMBL47986 |
CHEMBL1614364
(1)
|
1 / 1 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | CHEMBL47986 |
CHEMBL2114738
(1)
|
0 / 0 |
OMIM | preferred title | UniProt |
---|---|---|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#232300 | Glycogen storage disease ii |
P10253
|
#211980 | Lung cancer |
P00533
|
#158580 | Neuronopathy, distal hereditary motor, type viia; hmn7a |
Q9GZV3
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#604906 | Schizophrenia 9; sczd9 |
P49798
|
#181500 | Schizophrenia; sczd |
P49798
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | disease name | UniProt |
---|---|---|
H00016 | Oral cancer |
P00533
(related)
P00533 (marker) |
H00017 | Esophageal cancer |
P00533
(related)
|
H00018 | Gastric cancer |
P00533
(related)
|
H00022 | Bladder cancer |
P00533
(related)
|
H00028 | Choriocarcinoma |
P00533
(related)
|
H00030 | Cervical cancer |
P00533
(related)
|
H00042 | Glioma |
P00533
(related)
P00533 (marker) |
H00055 | Laryngeal cancer |
P00533
(related)
P00533 (marker) |
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|