| Organism name | Dittrichia graveolens (L.) GREUTER |
|---|---|
| Genus | Dittrichia |
| Family | Asteraceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Dittrichia |
|---|---|
| Linked NCBI taxonomy ID | 56524 |
| Linked level | genus |
| Family in NCBI taxonomy | Asteraceae |
|---|---|
| ID | 4210 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | asterids |
|---|---|
| ID | 71274 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00029526
|
4-epi-Isoinuviscolide
|
No. 69 | No. 38 |
|
||||
|
C00012947
|
Graveolide
/ (+)-Graveolide / 2,3-Dihydroaromaticin / [3aR-(3aalpha,4abeta,7aalpha,8alpha,9abeta)]-Decahydro-4a,8-dimethyl-3-methyleneazuleno[6,5-b]furan-2,5-dione |
CHEMBL359555
CHEMBL1911138 CHEMBL1911140 |
3 / 0 / 0 | No. 340 | No. 38 |
|
||
|
C00012852
|
Ilicic acid
/ Vachanic acid |
CHEMBL365824
CHEMBL408129 CHEMBL1434009 CHEMBL1562054 |
6 / 5 / 3 | No. 398 | No. 38 |
|
||
|
C00021118
|
Bigelovin
|
CHEMBL312003
CHEMBL270297 CHEMBL486196 CHEMBL486997 |
C099796
|
22 / 17 / 18 | No. 470 | No. 38 |
|
|
|
C00021117
|
8-epi-Helenalin
|
CHEMBL338474
CHEMBL354946 CHEMBL486996 CHEMBL1728820 CHEMBL1911137 |
37 / 36 / 29 | No. 495 | No. 38 |
|
||
|
C00012726
|
Isocostic acid
/ (+/-)-Isocostic acid / cis-1,2,3,4,4a,5,6,7-Octahydro-4a,8-dimethyl-alpha-methylene-2-naphthaleneacetic acid |
CHEMBL371833
|
No. 748 |
|
||||
|
C00003376
|
Tomentosin
/ Xanthalongin |
CHEMBL257513
CHEMBL483219 CHEMBL1164483 |
No. 857 | No. 38 |
|
|||
|
C00012727
|
Costic acid
/ Costus acid |
CHEMBL486398
|
No. 978 |
|
||||
|
C00012731
|
Viscic acid
/ 3alpha-Hydroxycostic acid / [2R-(2alpha,4aalpha,7beta,8abeta)]-Decahydro-7-hydroxy-4a-methyl-alpha,8-bis(methylene)-2-naphthaleneacetic acid |
No. 978 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q9UNA4 | DNA polymerase iota | Enzyme | C00012852 C00021117 C00021118 | 0 / 0 |
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00012852 C00021117 C00021118 | 0 / 0 |
| O75496 | Geminin | Unclassified protein | C00021117 C00021118 | 0 / 0 |
| P19838 | Nuclear factor NF-kappa-B p105 subunit | Transcription Factor | C00012947 C00021117 | 0 / 0 |
| P06746 | DNA polymerase beta | Enzyme | C00012852 C00021117 | 0 / 0 |
| Q00653 | Nuclear factor NF-kappa-B p100 subunit | Transcription Factor | C00012947 C00021117 | 0 / 0 |
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00021117 C00021118 | 1 / 0 |
| P30556 | Type-1 angiotensin II receptor | Angiotensin receptor | C00021117 C00021118 | 1 / 1 |
| P11473 | Vitamin D3 receptor | NR1I1 | C00021117 C00021118 | 2 / 3 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00021117 C00021118 | 0 / 0 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00021117 C00021118 | 0 / 0 |
| P42858 | Huntingtin | Unclassified protein | C00021117 C00021118 | 1 / 1 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00021117 C00021118 | 2 / 0 |
| Q99700 | Ataxin-2 | Unclassified protein | C00021117 C00021118 | 1 / 1 |
| P51151 | Ras-related protein Rab-9A | Unclassified protein | C00021117 C00021118 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00021117 C00021118 | 4 / 3 |
| Q9Y2T6 | G-protein coupled receptor 55 | Lysophosphatidylinositol receptor | C00021117 C00021118 | 0 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00021117 C00021118 | 0 / 0 |
| Q04206 | Transcription factor p65 | Transcription Factor | C00012947 C00021117 | 0 / 0 |
| Q9Y253 | DNA polymerase eta | Enzyme | C00021117 C00021118 | 1 / 1 |
| Q16637 | Survival motor neuron protein | Unclassified protein | C00012852 C00021117 | 4 / 1 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00021117 C00021118 | 0 / 0 |
| P17861 | X-box-binding protein 1 | Unclassified protein | C00021117 C00021118 | 1 / 0 |
| O15118 | Niemann-Pick C1 protein | Unclassified protein | C00021117 C00021118 | 1 / 1 |
| P28482 | Mitogen-activated protein kinase 1 | Erk | C00021117 C00021118 | 0 / 0 |
| Q00987 | E3 ubiquitin-protein ligase Mdm2 | Other nuclear protein | C00021117 C00021118 | 1 / 5 |
| P11308 | Transcriptional regulator ERG | Unclassified protein | C00012852 | 1 / 2 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00021117 | 0 / 0 |
| P06280 | Alpha-galactosidase A | Enzyme | C00021117 | 1 / 1 |
| P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00012852 | 0 / 0 |
| P38398 | Breast cancer type 1 susceptibility protein | Enzyme | C00021117 | 4 / 2 |
| Q92830 | Histone acetyltransferase KAT2A | Enzyme | C00021117 | 0 / 0 |
| P00352 | Retinal dehydrogenase 1 | Enzyme | C00021117 | 0 / 0 |
| Q9NUW8 | Tyrosyl-DNA phosphodiesterase 1 | Enzyme | C00021117 | 1 / 1 |
| Q9Y5X4 | Photoreceptor-specific nuclear receptor | NR2E3 | C00021117 | 2 / 2 |
| Q8IUX4 | DNA dC->dU-editing enzyme APOBEC-3F | Enzyme | C00021117 | 0 / 0 |
| P04062 | Glucosylceramidase | Enzyme | C00021117 | 6 / 4 |
| P49798 | Regulator of G-protein signaling 4 | Unclassified protein | C00021117 | 2 / 0 |
| P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00021117 | 0 / 3 |
| Q06710 | Paired box protein Pax-8 | Unclassified protein | C00021118 | 1 / 2 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #614401 | Accelerated tumor formation, susceptibility to; actfs |
Q00987
|
| #114480 | Breast cancer |
P38398
|
| #604370 | Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 |
P38398
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #268100 | Enhanced s-cone syndrome; escs |
Q9Y5X4
|
| #612219 | Ewing sarcoma; es |
P11308
|
| #301500 | Fabry disease |
P06280
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #608013 | Gaucher disease, perinatal lethal |
P04062
|
| #230800 | Gaucher disease, type i |
P04062
|
| #230900 | Gaucher disease, type ii |
P04062
|
| #231000 | Gaucher disease, type iii |
P04062
|
| #231005 | Gaucher disease, type iiic |
P04062
|
| #137800 | Glioma susceptibility 1; glm1 |
O75874
|
| #143100 | Huntington disease; hd |
P42858
|
| #218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #612371 | Major affective disorder 7; mafd7 |
P17861
|
| #607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
| #257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
| #167000 | Ovarian cancer |
P38398
|
| #614320 | Pancreatic cancer, susceptibility to, 4; pnca4 |
P38398
|
| #168600 | Parkinson disease, late-onset; pd |
P04062
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #267430 | Renal tubular dysgenesis; rtd |
P30556
|
| #611131 | Retinitis pigmentosa 37; rp37 |
Q9Y5X4
|
| #604906 | Schizophrenia 9; sczd9 |
P49798
|
| #181500 | Schizophrenia; sczd |
P49798
|
| #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
|
| #607250 | Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 |
Q9NUW8
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
| #278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
| KEGG | name | UniProt |
|---|---|---|
| H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
| H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
| H00082 | Graves' disease |
P01215
(marker)
|
| H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
Q06710 (related) |
| H00066 | Lewy body dementia (LBD) |
P04062
(related)
|
| H00126 | Gaucher disease |
P04062
(related)
|
| H00426 | Defects in the degradation of ganglioside |
P04062
(related)
|
| H00810 | Progressive myoclonic epilepsy (PME) |
P04062
(related)
|
| H00125 | Fabry disease |
P06280
(related)
|
| H00058 | Amyotrophic lateral sclerosis (ALS) |
P10636
(related)
|
| H00077 | Progressive supranuclear palsy (PSP) |
P10636
(related)
|
| H00078 | Frontotemporal lobar degeneration (FTLD) |
P10636
(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)
|
| H00575 | Renal tubular dysgenesis |
P30556
(related)
|
| H00027 | Ovarian cancer |
P38398
(related)
|
| H00031 | Breast cancer |
P38398
(related)
|
| H00059 | Huntington's disease (HD) |
P42858
(related)
|
| H00025 | Penile cancer |
Q00987
(related)
|
| H00028 | Choriocarcinoma |
Q00987
(related)
|
| H00036 | Osteosarcoma |
Q00987
(related)
|
| H00037 | Alveolar rhabdomyosarcoma |
Q00987
(related)
|
| H00042 | Glioma |
Q00987
(related)
|
| H00032 | Thyroid cancer |
Q06710
(related)
|
| H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
Q9NUW8 (related) |
| H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|
| H00527 | Retinitis pigmentosa (RP) |
Q9Y5X4
(related)
|
| H00805 | Vitreoretinal degeneration |
Q9Y5X4
(related)
|