Species

KNApSAcK Entry

Organism name Isodon scoparius
Genus Isodon
Family Labiatae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Isodon scoparius
Linked NCBI taxonomy ID 662927
Linked level species

Family

Family in NCBI taxonomy Lamiaceae
ID 4136

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (22)

KNApSAcK ID name ChEMBL link CTD link # of proteins in
ChEMBL interaction
/ related OMIM
/ related KEGG DISEASE
# of genes in
CTD interaction
/ related diseases
KCF-S
cluster
phytochemical
cluster
figure
C00034946 External link 512 Phyllostachysin D
/ (+)-Phyllostachysin D
CHEMBL562426
No. 132
C00034948 External link 512 Phyllostachysin F
/ (-)-Phyllostachysin F
CHEMBL1163642
No. 132
C00034949 External link 512 Phyllostachysin G
/ (-)-Phyllostachysin G
No. 132
C00034950 External link 512 Phyllostachysin H
/ (-)-Phyllostachysin H
CHEMBL563031
No. 132
C00034956 External link 512 Rabdoinflexin B
/ (-)-Rabdoinflexin B
CHEMBL550840
No. 132
C00034957 External link 512 Rabdokunmin D
/ (-)-Rabdokunmin D
CHEMBL562046
No. 132
C00034958 External link 512 Rabdoloxin A
CHEMBL549680
No. 132
C00034959 External link 512 Rabdoloxin B
CHEMBL551178
No. 132
C00042901 External link 512 Rabdokunmin C
CHEMBL511464
CHEMBL549681
No. 132
C00047232 External link 512 Excisanin K
No. 132
C00047298 External link 512 Macrocalyxin E
No. 132
C00047260 External link 512 Kamebanin
CHEMBL472437
18 / 28 / 25 No. 132
C00047259 External link 512 Isoscoparin L
/ (-)-Isoscoparin L
CHEMBL560643
No. 132
C00047258 External link 512 Isoscoparin K
/ (-)-Isoscoparin K
No. 132
C00047256 External link 512 Isoscoparin H
/ (+)-Isoscoparin H
CHEMBL551365
No. 132
C00047257 External link 512 Isoscoparin I
/ (-)-Isoscoparin I
CHEMBL563174
No. 132
C00047253 External link 512 Isoscoparin E
/ (-)-Isoscoparin E
No. 289 No. 41
C00047254 External link 512 Isoscoparin F
/ (+)-Isoscoparin F
CHEMBL564818
No. 289 No. 41
C00047341 External link 512 Rabdokunmin A
CHEMBL564723
No. 289 No. 41
C00047266 External link 512 Lasiokaurinol
CHEMBL551554
No. 339
C00047252 External link 512 Isoscoparin D
/ (+)-Isoscoparin D
CHEMBL562598
No. 3019
C00047255 External link 512 Isoscoparin G
/ (+)-Isoscoparin G
No. 3019

Human Protein / Gene in interactions

18 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q16637 Survival motor neuron protein Unclassified protein C00047260 4 / 1
Q99700 Ataxin-2 Unclassified protein C00047260 1 / 1
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily C00047260 1 / 4
P02545 Prelamin-A/C Unclassified protein C00047260 11 / 10
P11473 Vitamin D3 receptor NR1I1 C00047260 2 / 3
P42858 Huntingtin Unclassified protein C00047260 1 / 1
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00047260 2 / 0
O75496 Geminin Unclassified protein C00047260 0 / 0
P51151 Ras-related protein Rab-9A Unclassified protein C00047260 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00047260 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00047260 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00047260 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00047260 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00047260 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00047260 4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00047260 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00047260 1 / 0
Q06710 Paired box protein Pax-8 Unclassified protein C00047260 1 / 2

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (28)

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 DISEASE (25)

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)