class name | count |
---|---|
rosids | 2 |
eudicotyledons | 1 |
class name | count |
---|---|
Fabaceae | 2 |
Polygonaceae | 1 |
br08003 Category | # of metabolite |
---|---|
Anthrone type | 1 |
br08003 Category | KEGG ID | KNApSAcK ID |
---|---|---|
Anthrone type | C10404 | C00002863 |
KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
---|---|---|---|---|---|---|
C00002863
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Sennoside A
|
CHEMBL54481
CHEMBL448894 CHEMBL445268 CHEMBL1314924 CHEMBL1356785 CHEMBL1362935 CHEMBL1644069 |
58 / 59 / 53 |
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accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00002863 | 0 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00002863 | 1 / 1 |
P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00002863 | 2 / 0 |
P35354 | Prostaglandin G/H synthase 2 | Oxidoreductase | C00002863 | 0 / 3 |
P29466 | Caspase-1 | C14 | C00002863 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00002863 | 0 / 0 |
O75604 | Ubiquitin carboxyl-terminal hydrolase 2 | Enzyme | C00002863 | 0 / 0 |
P02545 | Prelamin-A/C | Unclassified protein | C00002863 | 11 / 10 |
P10828 | Thyroid hormone receptor beta | NR1A2 | C00002863 | 3 / 1 |
P54132 | Bloom syndrome protein | Enzyme | C00002863 | 1 / 2 |
P11473 | Vitamin D3 receptor | NR1I1 | C00002863 | 2 / 3 |
O15296 | Arachidonate 15-lipoxygenase B | Enzyme | C00002863 | 0 / 0 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00002863 | 2 / 2 |
P39748 | Flap endonuclease 1 | Enzyme | C00002863 | 0 / 0 |
Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00002863 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00002863 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00002863 | 0 / 0 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00002863 | 0 / 0 |
P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00002863 | 4 / 2 |
Q9Y253 | DNA polymerase eta | Enzyme | C00002863 | 1 / 1 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00002863 | 0 / 0 |
P11308 | Transcriptional regulator ERG | Unclassified protein | C00002863 | 1 / 2 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00002863 | 0 / 0 |
O94782 | Ubiquitin carboxyl-terminal hydrolase 1 | Enzyme | C00002863 | 0 / 0 |
P06280 | Alpha-galactosidase A | Enzyme | C00002863 | 1 / 1 |
P28482 | Mitogen-activated protein kinase 1 | Erk | C00002863 | 0 / 0 |
Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | C00002863 | 3 / 3 |
P15428 | 15-hydroxyprostaglandin dehydrogenase [NAD(+)] | Enzyme | C00002863 | 2 / 2 |
O15118 | Niemann-Pick C1 protein | Unclassified protein | C00002863 | 1 / 1 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00002863 | 0 / 0 |
P16050 | Arachidonate 15-lipoxygenase | Enzyme | C00002863 | 0 / 0 |
P55210 | Caspase-7 | C14 | C00002863 | 0 / 0 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002863 | 0 / 1 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00002863 | 0 / 0 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00002863 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00002863 | 4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002863 | 0 / 0 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00002863 | 0 / 0 |
B2RXH2 | Lysine-specific demethylase 4E | Enzyme | C00002863 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00002863 | 0 / 0 |
O00167 | Eyes absent homolog 2 | Enzyme | C00002863 | 0 / 0 |
Q2TB90 | Putative hexokinase HKDC1 | Enzyme | C00002863 | 0 / 0 |
Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00002863 | 0 / 0 |
Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00002863 | 1 / 1 |
O00255 | Menin | Unclassified protein | C00002863 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002863 | 1 / 2 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00002863 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00002863 | 1 / 4 |
Q92731 | Estrogen receptor beta | NR3A2 | C00002863 | 0 / 1 |
P03372 | Estrogen receptor | NR3A1 | C00002863 | 1 / 1 |
P19429 | Troponin I, cardiac muscle | Unclassified protein | C00002863 | 4 / 4 |
P45379 | Troponin T, cardiac muscle | Unclassified protein | C00002863 | 3 / 5 |
P63316 | Troponin C, slow skeletal and cardiac muscles | Other cytosolic protein | C00002863 | 2 / 2 |
P63165 | Small ubiquitin-related modifier 1 | Unclassified protein | C00002863 | 1 / 1 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00002863 | 0 / 0 |
Q9H0H5 | Rac GTPase-activating protein 1 | Unclassified protein | C00002863 | 0 / 0 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00002863 | 2 / 1 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00002863 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#210900 | Bloom syndrome; blm |
P54132
|
#114480 | Breast cancer |
P38398
|
#604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 |
P38398
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#601494 | Cardiomyopathy, dilated, 1d; cmd1d |
P45379
|
#613286 | Cardiomyopathy, dilated, 1ff; cmd1ff |
P19429
|
#611879 | Cardiomyopathy, dilated, 1z; cmd1z |
P63316
|
#611880 | Cardiomyopathy, dilated, 2a; cmd2a |
P19429
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#613243 | Cardiomyopathy, familial hypertrophic, 13; cmh13 |
P63316
|
#115195 | Cardiomyopathy, familial hypertrophic, 2; cmh2 |
P45379
|
#613690 | Cardiomyopathy, familial hypertrophic, 7; cmh7 |
P19429
|
#115210 | Cardiomyopathy, familial restrictive, 1; rcm1 |
P19429
|
#612422 | Cardiomyopathy, familial restrictive, 3; rcm3 |
P45379
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#114500 | Colorectal cancer; crc |
P84022
Q14191 |
#119900 | Digital clubbing, isolated congenital |
P15428
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#615363 | Estrogen resistance; estrr |
P03372
|
#612219 | Ewing sarcoma; es |
P11308
|
#301500 | Fabry disease |
P06280
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#145000 | Hyperparathyroidism 1; hrpt1 |
O00255
|
#259100 | Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 |
P15428
|
#151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
#613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
#248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
#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
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
#613705 | Orofacial cleft 10; ofc10 |
P63165
|
#167000 | Ovarian cancer |
P38398
|
#614320 | Pancreatic cancer, susceptibility to, 4; pnca4 |
P38398
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#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
|
#188570 | Thyroid hormone resistance, generalized, autosomal dominant; grth |
P10828
|
#274300 | Thyroid hormone resistance, generalized, autosomal recessive; grth |
P10828
|
#145650 | Thyroid hormone resistance, selective pituitary; prth |
P10828
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | 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)
|
H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(related)
P19429 (related) P45379 (related) P63316 (related) |
H00420 | Familial partial lipodystrophy (FPL) |
P02545
(related)
|
H00563 | Emery-Dreifuss muscular dystrophy |
P02545
(related)
|
H00590 | Congenital muscular dystrophies (CMD/MDC) |
P02545
(related)
|
H00593 | Limb-girdle muscular dystrophy (LGMD) |
P02545
(related)
|
H00601 | Hutchinson-Gilford progeria syndrome |
P02545
(related)
|
H00663 | Restrictive dermopathy |
P02545
(related)
|
H00665 | Mandibuloacral dysplasia |
P02545
(related)
|
H01216 | Left ventricular noncompaction (LVNC) |
P02545
(related)
P45379 (related) |
H00026 | Endometrial Cancer |
P03372
(marker)
Q92731 (marker) |
H00125 | Fabry disease |
P06280
(related)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
Q13148 (related) |
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00249 | Thyroid hormone resistance syndrome |
P10828
(related)
|
H00024 | Prostate cancer |
P11308
(related)
|
H00035 | Ewing's sarcoma |
P11308
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H00457 | Primary hypertrophic osteoarthropathy (PHO) |
P15428
(related)
|
H01246 | Isolated congenital nail clubbing (ICNC) |
P15428
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H00292 | Hypertrophic cardiomyopathy (HCM) |
P19429
(related)
P45379 (related) P63316 (related) |
H01219 | Restrictive cardiomyopathy (RCM) |
P19429
(related)
P45379 (related) |
H00295 | Viral myocarditis |
P19429
(marker)
P45379 (marker) |
H00017 | Esophageal cancer |
P35354
(related)
|
H00025 | Penile cancer |
P35354
(related)
|
H00046 | Cholangiocarcinoma |
P35354
(related)
|
H00027 | Ovarian cancer |
P38398
(related)
|
H00031 | Breast cancer |
P38398
(related)
|
H00094 | DNA repair defects |
P54132
(related)
|
H00296 | Defects in RecQ helicases |
P54132
(related)
Q14191 (related) |
H00516 | Isolated orofacial clefts |
P63165
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) Q03164 (related) Q03164 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
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)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|