class name | count |
---|---|
asterids | 51 |
class name | count |
---|---|
Lamiaceae | 51 |
br08003 Category | # of metabolite |
---|
br08003 Category | KEGG ID | KNApSAcK ID |
---|
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 |
---|---|---|---|---|---|---|
C00032524
![]() |
Xindongnin I
/ (-)-Xindongnin I |
![]() |
||||
C00032525
![]() |
Xindongnin J
|
![]() |
||||
C00034946
![]() |
Phyllostachysin D
/ (+)-Phyllostachysin D |
CHEMBL562426
|
![]() |
|||
C00034948
![]() |
Phyllostachysin F
/ (-)-Phyllostachysin F |
CHEMBL1163642
|
![]() |
|||
C00034949
![]() |
Phyllostachysin G
/ (-)-Phyllostachysin G |
![]() |
||||
C00034950
![]() |
Phyllostachysin H
/ (-)-Phyllostachysin H |
CHEMBL563031
|
![]() |
|||
C00034956
![]() |
Rabdoinflexin B
/ (-)-Rabdoinflexin B |
CHEMBL550840
|
![]() |
|||
C00034957
![]() |
Rabdokunmin D
/ (-)-Rabdokunmin D |
CHEMBL562046
|
![]() |
|||
C00034958
![]() |
Rabdoloxin A
|
CHEMBL549680
|
![]() |
|||
C00034959
![]() |
Rabdoloxin B
|
CHEMBL551178
|
![]() |
|||
C00038398
![]() |
Alboatisin A
/ (-)-Alboatisin A |
CHEMBL376585
|
![]() |
|||
C00038399
![]() |
Alboatisin B
/ (-)-Alboatisin B |
CHEMBL228664
|
![]() |
|||
C00038400
![]() |
Alboatisin C
/ (-)-Alboatisin C |
CHEMBL388775
|
![]() |
|||
C00039416
![]() |
Inflexarabdonin I
|
CHEMBL224372
|
![]() |
|||
C00039996
![]() |
Phyllostachysin A
|
CHEMBL250051
|
![]() |
|||
C00040684
![]() |
Xerophilusin F
/ (+)-Xerophilusin F |
CHEMBL401393
|
![]() |
|||
C00040685
![]() |
Xerophilusin II
/ (+)-Xerophilusin II |
CHEMBL401391
|
![]() |
|||
C00042211
![]() |
Albopilosin E
/ (+)-Albopilosin E |
CHEMBL456312
|
![]() |
|||
C00042212
![]() |
Albopilosin F
/ (-)-Albopilosin F |
CHEMBL456523
|
![]() |
|||
C00042214
![]() |
Albopilosin H
/ (-)-Albopilosin H |
CHEMBL458481
|
![]() |
|||
C00042215
![]() |
Albopilosin I
/ (-)-Albopilosin I |
CHEMBL458479
|
![]() |
|||
C00042225
![]() |
Amethystonoic acid
/ (-)-Amethystonoic acid |
CHEMBL516840
|
![]() |
|||
C00042404
![]() |
Coetsanoic acid
|
CHEMBL518072
|
![]() |
|||
C00042716
![]() |
Macrocalyxin C
/ (-)-Amethystonal |
CHEMBL463149
|
C077959
|
![]() |
||
C00042901
![]() |
Rabdokunmin C
|
CHEMBL511464
CHEMBL549681 |
![]() |
|||
C00047232
![]() |
Excisanin K
|
![]() |
||||
C00047256
![]() |
Isoscoparin H
/ (+)-Isoscoparin H |
CHEMBL551365
|
![]() |
|||
C00047257
![]() |
Isoscoparin I
/ (-)-Isoscoparin I |
CHEMBL563174
|
![]() |
|||
C00047258
![]() |
Isoscoparin K
/ (-)-Isoscoparin K |
![]() |
||||
C00047259
![]() |
Isoscoparin L
/ (-)-Isoscoparin L |
CHEMBL560643
|
![]() |
|||
C00047260
![]() |
Kamebanin
|
CHEMBL472437
|
18 / 28 / 25 |
![]() |
||
C00047298
![]() |
Macrocalyxin E
|
![]() |
||||
C00047363
![]() |
3-Epipseurata B
/ (-)-3-Epipseurata B |
CHEMBL564375
CHEMBL557031 |
![]() |
|||
C00047479
![]() |
Kamebanin
|
CHEMBL472437
|
18 / 28 / 25 |
![]() |
||
C00047517
![]() |
Minheryin G
/ (-)-Minheryin G |
CHEMBL562256
|
![]() |
|||
C00047547
![]() |
Pseurata A
|
CHEMBL2021467
CHEMBL2021470 |
![]() |
|||
C00047548
![]() |
Pseurata B
|
CHEMBL564375
CHEMBL557031 |
![]() |
|||
C00047616
![]() |
Wangzaozin A
|
CHEMBL2021467
CHEMBL2021470 |
![]() |
|||
C00050357
![]() |
Excisanin F
/ (+)-Excisanin F |
![]() |
||||
C00050358
![]() |
Excisanin G
/ (-)-Excisanin G |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q16637 | Survival motor neuron protein | Unclassified protein | C00047260 C00047479 | 4 / 1 |
Q99700 | Ataxin-2 | Unclassified protein | C00047260 C00047479 | 1 / 1 |
Q13315 | Serine-protein kinase ATM | Atypical serine/threonine protein kinase PIKK subfamily | C00047260 C00047479 | 1 / 4 |
P02545 | Prelamin-A/C | Unclassified protein | C00047260 C00047479 | 11 / 10 |
P11473 | Vitamin D3 receptor | NR1I1 | C00047260 C00047479 | 2 / 3 |
P42858 | Huntingtin | Unclassified protein | C00047260 C00047479 | 1 / 1 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00047260 C00047479 | 2 / 0 |
O75496 | Geminin | Unclassified protein | C00047260 C00047479 | 0 / 0 |
P51151 | Ras-related protein Rab-9A | Unclassified protein | C00047260 C00047479 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00047260 C00047479 | 0 / 0 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00047260 C00047479 | 0 / 0 |
Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00047260 C00047479 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00047260 C00047479 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00047260 C00047479 | 0 / 0 |
P10636 | Microtubule-associated protein tau | Unclassified protein | C00047260 C00047479 | 4 / 3 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00047260 C00047479 | 0 / 0 |
O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00047260 C00047479 | 1 / 0 |
Q06710 | Paired box protein Pax-8 | Unclassified protein | C00047260 C00047479 | 1 / 2 |
OMIM | preferred title | UniProt |
---|---|---|
#208900 | Ataxia-telangiectasia; at |
Q13315
|
#115200 | Cardiomyopathy, dilated, 1a; cmd1a |
P02545
|
#212112 | Cardiomyopathy, dilated, with hypergonadotropic hypogonadism |
P02545
|
#605588 | Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 |
P02545
|
#114500 | Colorectal cancer; crc |
P84022
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#600274 | Frontotemporal dementia; ftd |
P10636
|
#137800 | Glioma susceptibility 1; glm1 |
O75874
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#143100 | Huntington disease; hd |
P42858
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
#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
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#260540 | Parkinson-dementia syndrome |
P10636
|
#172700 | Pick disease of brain |
P10636
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#253300 | Spinal muscular atrophy, type i; sma1 |
Q16637
|
#253550 | Spinal muscular atrophy, type ii; sma2 |
Q16637
|
#253400 | Spinal muscular atrophy, type iii; sma3 |
Q16637
|
#271150 | Spinal muscular atrophy, type iv; sma4 |
Q16637
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
KEGG | name | UniProt |
---|---|---|
H00264 | Charcot-Marie-Tooth disease (CMT) |
P02545
(related)
|
H00294 | Dilated cardiomyopathy (DCM) |
P02545
(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)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H00059 | Huntington's disease (HD) |
P42858
(related)
|
H00032 | Thyroid cancer |
Q06710
(related)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
Q06710
(related)
|
H00005 | Chronic lymphocytic leukemia (CLL) |
Q13315
(related)
|
H00064 | Ataxia telangiectasia (AT) |
Q13315
(related)
|
H00094 | DNA repair defects |
Q13315
(related)
|
H00848 | Ataxia with ocular apraxia (AOA) |
Q13315
(related)
|
H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|