Species

KNApSAcK Entry

Organism name Helichrysum forskahlii
Genus Helichrysum
Family Asteraceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Helichrysum forskahlii
Linked NCBI taxonomy ID 630302
Linked level species

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 (20)

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
C00004632 External link 512 Quercetin 3-methyl ether
/ Quercetin 3-O-methyl ether
CHEMBL163316
32 / 21 / 21 No. 3 No. 15
C00019064 External link 512 Oleanolic acid
/ Astrantiagenin C
/ Virgaureagenin B
/ 3beta-Hydroxyolean-12-en-28-oic acid
CHEMBL56615
CHEMBL168
CHEMBL180553
CHEMBL365375
CHEMBL486382
CHEMBL1413646
CHEMBL1436454
D009828
30 / 8 / 12 21 / 15 No. 13 No. 51
C00003738 External link 512 beta-Amyrin
/ beta-Amirin
/ beta-Amyrine
/ beta-Amyrenol
C036380
0 / 4 No. 23 No. 51
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
C00000965 External link 512 Glabranin
CHEMBL253998
CHEMBL488888
5 / 2 / 3 No. 28 No. 14
C00033902 External link 512 Helichrysone C
/ (+)-Helichrysone C
No. 28 No. 14
C00008189 External link 512 7-O-Prenylpinocembrin
No. 28 No. 14
C00008171 External link 512 Isoglabranin
/ 6-Prenylpinocembrin
/ 5,7-Dihydroxy-6-C-prenylflavanone
CHEMBL2143430
CHEMBL2165236
1 / 0 / 0 No. 28 No. 14
C00033901 External link 512 Helichrysone B
No. 90 No. 13
C00006935 External link 512 Cardamomin
CHEMBL378104
13 / 18 / 14 No. 92 No. 13
C00006933 External link 512 2',4',6'-Trihydroxychalcone
CHEMBL129371
2 / 0 / 3 No. 92 No. 13
C00007086 External link 512 2',6'-Dihydroxy-4'-prenyloxychalcone
No. 133 No. 13
C00007087 External link 512 2'-Hydroxy-6'-methoxy-4'-prenyloxychalcone
No. 133 No. 13
C00033900 External link 512 Helichrysone A
No. 133 No. 13
C00033565 External link 512 Acetyloleanolic acid
/ Oleanolic acid acetate
/ 3-O-Acetyloleanolic acid
/ (+)-Acetyloleanolic acid
/ (+)-Oleanolic acid acetate
/ (+)-3-O-Acetyloleanolic acid
/ 3beta-Acetoxyolean-12-en-28-oic acid
CHEMBL486822
CHEMBL494653
CHEMBL1315416
C052658
1 / 0 / 0 No. 177
C00033563 External link 512 3'',3''-Dimethyl-5',6'-pyrano-2',4'-dihydroxychalcone
No. 337
C00033772 External link 512 Desmethylhelichromanochalcone
No. 337
C00007983 External link 512 3',4',6'-Trihydroxy-2'-oxo-3',5'-diprenyldihydrochalcone
No. 2813
C00007984 External link 512 Helihumulone
No. 2813

Human Protein / Gene in interactions

70 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00000992 C00004632 C00006935 1 / 2
O75496 Geminin Unclassified protein C00004632 C00006935 C00019064 0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000992 C00004632 C00019064 0 / 0
Q9UNA4 DNA polymerase iota Enzyme C00004632 C00006935 C00019064 0 / 0
O00255 Menin Unclassified protein C00000992 C00004632 C00006935 2 / 5
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000992 C00004632 C00019064 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000992 C00004632 C00006935 4 / 3
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000965 C00000992 1 / 1
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00006933 C00019064 0 / 3
O75164 Lysine-specific demethylase 4A Enzyme C00004632 C00006935 0 / 0
Q99700 Ataxin-2 Unclassified protein C00004632 C00006935 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000965 C00000992 0 / 1
P06746 DNA polymerase beta Enzyme C00004632 C00019064 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00019064 C00033565 0 / 0
Q9UIF8 Bromodomain adjacent to zinc finger domain protein 2B Unclassified protein C00004632 C00006935 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00000992 C00004632 3 / 3
P11309 Serine/threonine-protein kinase pim-1 Pim C00000965 C00000992 0 / 0
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00004632 C00006935 0 / 0
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00006933 C00019064 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000992 C00006935 7 / 3
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000965 C00000992 0 / 1
P15121 Aldose reductase Enzyme C00004632 C00019064 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000965 C00000992 1 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00004632 C00006935 2 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000992 C00019064 0 / 0
P39748 Flap endonuclease 1 Enzyme C00004632 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00019064 0 / 0
P42858 Huntingtin Unclassified protein C00004632 1 / 1
Q9NR56 Muscleblind-like protein 1 Unclassified protein C00004632 1 / 0
P54132 Bloom syndrome protein Enzyme C00004632 1 / 2
P04792 Heat shock protein beta-1 Unclassified protein C00004632 2 / 1
P49841 Glycogen synthase kinase-3 beta Gsk C00019064 0 / 0
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00008171 0 / 0
P10586 Receptor-type tyrosine-protein phosphatase F Receptor tyrosine-protein phosphatase C00019064 0 / 0
Q9Y253 DNA polymerase eta Enzyme C00004632 1 / 1
P51452 Dual specificity protein phosphatase 3 Ser_Thr_Tyr C00019064 0 / 0
P04798 Cytochrome P450 1A1 Cytochrome P450 1A1 C00000992 0 / 0
P11021 78 kDa glucose-regulated protein Unclassified protein C00004632 0 / 0
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00019064 2 / 2
Q16678 Cytochrome P450 1B1 Cytochrome P450 1B1 C00000992 4 / 4
Q96RI1 Bile acid receptor NR1H4 C00019064 0 / 0
P18433 Receptor-type tyrosine-protein phosphatase alpha Receptor tyrosine-protein phosphatase C00019064 0 / 0
P35236 Tyrosine-protein phosphatase non-receptor type 7 Tyr C00019064 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000992 0 / 0
P07550 Beta-2 adrenergic receptor Adrenergic receptor C00004632 0 / 1
P08047 Transcription factor Sp1 Unclassified protein C00000992 0 / 0
P35228 Nitric oxide synthase, inducible Enzyme C00019064 1 / 1
Q8TDU6 G-protein coupled bile acid receptor 1 Steroid-like ligand receptor C00019064 0 / 0
P24666 Low molecular weight phosphotyrosine protein phosphatase Tyr C00019064 0 / 0
Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 Enzyme C00000992 0 / 0
Q6W5P4 Neuropeptide S receptor Neuropeptide receptor C00006935 1 / 0
Q06124 Tyrosine-protein phosphatase non-receptor type 11 Tyr C00019064 4 / 2
P10253 Lysosomal alpha-glucosidase Hydrolase C00004632 1 / 1
P22001 Potassium voltage-gated channel subfamily A member 3 KCNA, Kv1.x (Shaker) C00006935 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00004632 0 / 0
P17706 Tyrosine-protein phosphatase non-receptor type 2 Tyr C00019064 0 / 1
P29350 Tyrosine-protein phosphatase non-receptor type 6 Tyr C00019064 0 / 0
P04054 Phospholipase A2 Enzyme C00019064 0 / 0
P23469 Receptor-type tyrosine-protein phosphatase epsilon Receptor tyrosine-protein phosphatase C00019064 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00004632 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00004632 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00004632 0 / 0
Q8IUX4 DNA dC->dU-editing enzyme APOBEC-3F Enzyme C00004632 0 / 0
O60218 Aldo-keto reductase family 1 member B10 Enzyme C00019064 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00019064 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00019064 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00019064 1 / 4
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00004632 0 / 0
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00004632 0 / 0
Q14191 Werner syndrome ATP-dependent helicase Enzyme C00004632 2 / 1

24 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 C00019064
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 C00019064
3065 HDAC1, GON-10, HD1, RPD3, RPD3L1 histone deacetylase 1 (EC:3.5.1.98) C00019064
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
177 AGER, RAGE advanced glycosylation end product-specific receptor C00019064
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00019064
841 CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) C00019064
847 CAT catalase (EC:1.11.1.6) C00019064
595 CCND1, BCL1, D11S287E, PRAD1, U21B31 cyclin D1 C00019064
1544 CYP1A2, CP12, P3-450, P450(PA) cytochrome P450, family 1, subfamily A, polypeptide 2 (EC:1.14.14.1) C00019064
1576 CYP3A4, CP33, CP34, CYP3A, CYP3A3, CYPIIIA3, CYPIIIA4, HLP, NF-25, P450C3, P450PCN1 cytochrome P450, family 3, subfamily A, polypeptide 4 (EC:1.14.13.67 1.14.13.97 1.14.13.32 1.14.13.157) C00019064
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
3146 HMGB1, HMG1, HMG3, SBP-1 high mobility group box 1 C00019064
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00019064
4233 MET, AUTS9, HGFR, RCCP2, c-Met met proto-oncogene (EC:2.7.10.1) C00019064
4780 NFE2L2, NRF2 nuclear factor, erythroid 2-like 2 C00019064
5052 PRDX1, MSP23, NKEF-A, NKEFA, PAG, PAGA, PAGB, PRX1, PRXI, TDPX2 peroxiredoxin 1 (EC:1.11.1.15) C00019064
5728 PTEN, 10q23del, BZS, CWS1, DEC, GLM2, MHAM, MMAC1, PTEN1, TEP1 phosphatase and tensin homolog (EC:3.1.3.67 3.1.3.16 3.1.3.48) C00019064
6401 SELE, CD62E, ELAM, ELAM1, ESEL, LECAM2 selectin E C00019064
7124 TNF, DIF, TNF-alpha, TNFA, TNFSF2 tumor necrosis factor C00019064
7150 TOP1, TOPI topoisomerase (DNA) I (EC:5.99.1.2) C00019064
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00019064
7412 VCAM1, CD106, INCAM-100 vascular cell adhesion molecule 1 C00019064

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (43)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#608584 Asthma-related traits, susceptibility to, 2 Q6W5P4
#210900 Bloom syndrome; blm P54132
#606595 Charcot-marie-tooth disease, axonal, type 2f; cmt2f P04792
#114500 Colorectal cancer; crc P84022
Q14191
#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
#232300 Glycogen storage disease ii P10253
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#143100 Huntington disease; hd P42858
#145000 Hyperparathyroidism 1; hrpt1 O00255
#607785 Juvenile myelomonocytic leukemia; jmml Q06124
#151100 Leopard syndrome 1 Q06124
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#611162 Malaria, susceptibility to P35228
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#156250 Metachondromatosis; metcds Q06124
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#160900 Myotonic dystrophy 1; dm1 Q9NR56
#608634 Neuronopathy, distal hereditary motor, type iib; hmn2b P04792
#163950 Noonan syndrome 1; ns1 Q06124
#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
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#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
#277700 Werner syndrome; wrn Q14191
#278750 Xeroderma pigmentosum, variant type; xpv Q9Y253

KEGG DISEASE (42)

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)
H00856 Distal hereditary motor neuropathies (dHMN) P04792 (related)
H00079 Asthma P07550 (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)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P11511 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00408 Type I diabetes mellitus P17706 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00017 Esophageal cancer P35228 (related)
P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00059 Huntington's disease (HD) P42858 (related)
H00094 DNA repair defects P54132 (related)
H00296 Defects in RecQ helicases P54132 (related)
Q14191 (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) 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)
H00523 Noonan syndrome and related disorders Q06124 (related)
H01018 Metachondromatosis Q06124 (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)
H00403 Disorders of nucleotide excision repair Q9Y253 (related)

Diseases related to CTD interactions

18 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D007249 Inflammation C00003738
C00019064
D007674 Kidney Diseases C00019064
D005157 Facial Pain C00003738
D010146 Pain C00003738
D002252 Carbon Tetrachloride Poisoning C00019064
D056486 Drug-Induced Liver Injury C00019064
D050171 Dyslipidemias C00019064
D018149 Glucose Intolerance C00019064
D006949 Hyperlipidemias C00019064
D006930 Hyperalgesia C00003738
D008103 Liver Cirrhosis C00019064
D008106 Liver Cirrhosis, Experimental C00019064
D008107 Liver Diseases C00019064
D017202 Myocardial Ischemia C00019064
D009369 Neoplasms C00019064
D009765 Obesity C00019064
D011041 Poisoning C00019064
D011230 Precancerous Conditions C00019064