Species

KNApSAcK Entry

Organism name Helichrysum spp.
Genus Helichrysum
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Helichrysum
Linked NCBI taxonomy ID 59430
Linked level genus

Family

Family in NCBI taxonomy Asteraceae
ID 4210

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (15)

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
C00004588 External link 512 3,5-Dihydroxy-6,7,8-trimethoxyflavone
/ 3,5-Dihydroxy-6,7,8-trimethoxy-2-phenyl-4H-1-benzopyran-4-one
CHEMBL1416487
8 / 13 / 7 No. 3 No. 15
C00004684 External link 512 Axillarin
/ Quercetagetin 3,6-dimethyl ether
/ 3,6-Dimethoxy-5,7,3',4'-tetrahydroxyflavone
/ 2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3,6-dimethoxy-4H-1-benzopyran-4-one
CHEMBL487810
C056669
1 / 1 / 1 No. 3 No. 15
C00003879 External link 512 Xanthomicrol
/ 5-Hydroxy-2-(4-hydroxyphenyl)-6,7,8-trimethoxy-4H-1-benzopyran-4-one
CHEMBL476121
C462036
No. 3 No. 15
C00003926 External link 512 5,7,3',4'-Tetrahydroxy-6,8-dimethoxyflavone
No. 3 No. 15
C00004585 External link 512 3,5,7-Trihydroxy-6,8-dimethoxyflavone
/ 3,5,7-Trihydroxy-6,8-dimethoxy-2-phenyl-4H-1-benzopyran-4-one
No. 3 No. 15
C00004544 External link 512 3-O-Methylalnusin
/ Alnusin 3-methyl ether
/ 5,7-Dihydroxy-3,6-dimethoxyflavone
/ 5,7-Dihydroxy-3,6-dimethoxy-2-phenyl-4H-1-benzopyran-4-one
No. 3 No. 15
C00003927 External link 512 Sideritiflavone
/ 5,3',4'-Trihydroxy-6,7,8-trimethoxyflavone
/ 2-(3,4-Dihydroxyphenyl)-5-hydroxy-6,7,8-trimethoxy-4H-1-benzopyran-4-one
CHEMBL312790
No. 3 No. 15
C00004793 External link 512 5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone
/ 5,4',5'-Trihydroxy-3,6,7,8-tetramethoxyflavone
/ 2-(3,4-Dihydroxyphenyl)-5-hydroxy-3,6,7,8-tetramethoxy-4H-1-benzopyran-4-one
CHEMBL471084
C037412
No. 8 No. 15
C00008204 External link 512 Floribundoside
CHEMBL2152489
CHEMBL2152490
No. 12 No. 14
C00000992 External link 512 Pinocembrin
CHEMBL70518
CHEMBL399910
CHEMBL399249
C016063
18 / 23 / 23 5 / 0 No. 25 No. 14
C00008143 External link 512 Alpinetin
/ (-)-Alpinetin
CHEMBL427218
CHEMBL254825
No. 25 No. 14
C00008171 External link 512 Isoglabranin
/ 6-Prenylpinocembrin
/ 5,7-Dihydroxy-6-C-prenylflavanone
CHEMBL2143430
CHEMBL2165236
1 / 0 / 0 No. 28 No. 14
C00006935 External link 512 Cardamomin
CHEMBL378104
13 / 18 / 14 No. 92 No. 13
C00006934 External link 512 Pinostrobin chalcone
/ 2',6'-Dihydroxy-4'-methoxychalcone
CHEMBL317221
CHEMBL1705800
3 / 1 / 2 No. 92 No. 13
C00002399 External link 512 6-Hydroxytremetone
No. 1831

Human Protein / Gene in interactions

33 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10636 Microtubule-associated protein tau Unclassified protein C00000992 C00004588 C00006935 4 / 3
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000992 C00004588 C00006935 7 / 3
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000992 C00006934 1 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000992 C00006934 0 / 0
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000992 C00006935 1 / 2
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000992 C00004588 0 / 0
O00255 Menin Unclassified protein C00000992 C00006935 2 / 5
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00004588 C00008171 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000992 C00006934 0 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00000992 0 / 0
P11309 Serine/threonine-protein kinase pim-1 Pim C00000992 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00004588 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00006935 2 / 0
O75496 Geminin Unclassified protein C00006935 0 / 0
P47989 Xanthine dehydrogenase/oxidase Oxidoreductase C00004684 1 / 1
P08047 Transcription factor Sp1 Unclassified protein C00000992 0 / 0
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00000992 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00006935 0 / 0
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00000992 4 / 4
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000992 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000992 3 / 3
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00000992 0 / 0
P10253 Lysosomal alpha-glucosidase Hydrolase C00004588 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000992 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00006935 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00006935 1 / 0
O75164 Lysine-specific demethylase 4A Enzyme C00006935 0 / 0
P22001 Potassium voltage-gated channel subfamily A member 3 KCNA, Kv1.x (Shaker) C00006935 0 / 0
Q99700 Ataxin-2 Unclassified protein C00006935 1 / 1
B2RXH2 Lysine-specific demethylase 4E Enzyme C00004588 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00004588 1 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00006935 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000992 1 / 0

5 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
5594 MAPK1, ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk mitogen-activated protein kinase 1 (EC:2.7.11.24) C00000992
5595 MAPK3, ERK-1, ERK1, ERT2, HS44KDAP, HUMKER1A, P44ERK1, P44MAPK, PRKM3, p44-ERK1, p44-MAPK mitogen-activated protein kinase 3 (EC:2.7.11.24) C00000992
6817 SULT1A1, HAST1/HAST2, P-PST, PST, ST1A1, ST1A3, STP, STP1, TSPST1 sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (EC:2.8.2.1) C00000992
6818 SULT1A3, HAST, HAST3, M-PST, ST1A3/ST1A4, ST1A5, STM, TL-PST sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3 (EC:2.8.2.1) C00000992
7052 TGM2, G-ALPHA-h, GNAH, TG2, TGC transglutaminase 2 (EC:2.3.2.13) C00000992

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (30)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#600274 Frontotemporal dementia; ftd P10636
#137750 Glaucoma 1, open angle, a; glc1a Q16678
#231300 Glaucoma 3, primary congenital, a; glc3a Q16678
#137760 Glaucoma, primary open angle; poag Q16678
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#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
#166350 Osseous heteroplasia, progressive; poh P63092
#260540 Parkinson-dementia syndrome P10636
#604229 Peters anomaly Q16678
#172700 Pick disease of brain P10636
#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
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#278300 Xanthinuria, type i P47989

KEGG DISEASE (26)

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)
H00036 Osteosarcoma P08684 (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)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00192 Xanthinuria P47989 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)
H00612 Primary open angle glaucoma Q16678 (related)
H01075 Peters anomaly Q16678 (related)
H01159 Anterior segment dysgenesis (ASD) Q16678 (related)
H01203 Primary congenital glaucoma (PCG) Q16678 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (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)