| Organism name | Thujopsis dolabrata |
|---|---|
| Genus | Thujopsis |
| Family | Cupressaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Thujopsis dolabrata |
|---|---|
| Linked NCBI taxonomy ID | 13727 |
| Linked level | species |
| Family in NCBI taxonomy | Cupressaceae |
|---|---|
| ID | 3367 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | Spermatophyta |
|---|---|
| ID | 58024 |
| 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 |
|---|---|---|---|---|---|---|---|---|
|
C00008695
|
(2R,3S)-Epitaxifolin 3-xyloside
|
CHEMBL2332674
CHEMBL2332675 CHEMBL2332676 CHEMBL2332677 |
No. 12 | No. 14 |
|
|||
|
C00008694
|
(2R,3R)-Taxifolin 3-xyloside
|
CHEMBL2332674
CHEMBL2332675 CHEMBL2332676 CHEMBL2332677 |
No. 12 | No. 14 |
|
|||
|
C00008696
|
(2S,3R)-Epitaxifolin 3-xyloside
|
CHEMBL2332674
CHEMBL2332675 CHEMBL2332676 CHEMBL2332677 |
No. 12 | No. 14 |
|
|||
|
C00008697
|
(2S,3S)-Taxifolin 3-xyloside
|
CHEMBL2332674
CHEMBL2332675 CHEMBL2332676 CHEMBL2332677 |
No. 12 | No. 14 |
|
|||
|
C00009089
|
Arecatannin B1
|
CHEMBL592329
|
2 / 3 / 4 | No. 29 | No. 19 |
|
||
|
C00006537
|
Chamaecyparin
|
No. 34 | No. 18 |
|
||||
|
C00006536
|
Cryptomerin A
|
No. 34 | No. 18 |
|
||||
|
C00012750
|
(+)-Costal
/ Costic aldehyde / (+)-beta-Costal / Eudesma-4(14),11(13)-dien-12-al |
CHEMBL362552
|
No. 151 | No. 38 |
|
|||
|
C00022707
|
Isoagatholal
|
No. 165 |
|
|||||
|
C00012509
|
gamma-Cuparenol
|
No. 309 |
|
|||||
|
C00003194
|
Thujopsene
|
No. 365 | No. 38 |
|
||||
|
C00002616
|
beta-Peltatin A methyl ether
|
CHEMBL483004
|
C010499
|
No. 427 | No. 21 |
|
||
|
C00007208
|
beta-Peltatin
/ (-)-beta-Peltatin |
CHEMBL97543
CHEMBL443566 CHEMBL1435754 |
9 / 16 / 14 | No. 427 | No. 21 |
|
||
|
C00002597
|
Deoxypodophyllotoxin
/ (-)-Deoxypodophyllotoxin |
CHEMBL63970
CHEMBL149525 CHEMBL152144 CHEMBL255919 CHEMBL519603 CHEMBL476679 CHEMBL1736070 |
7 / 4 / 2 | No. 427 | No. 21 |
|
||
|
C00012529
|
4-Cuprenene
/ Buprenene IV / gamma-Cuprenene |
No. 451 | No. 38 |
|
||||
|
C00021952
|
Isowiddrene
/ alpha-Pseudowiddrene |
No. 451 | No. 38 |
|
||||
|
C00012528
|
Cuprenene
/ 2-Cuprenene / Cuprenene 2 / Cuprenene III |
No. 451 | No. 38 |
|
||||
|
C00002608
|
Hinokinin
/ Hinoquinin / (-)-Hinokinin / (-)-Hinoquinin |
CHEMBL180970
CHEMBL182073 CHEMBL242011 |
C475934
|
2 / 1 / 1 | No. 629 | No. 21 |
|
|
|
C00012018
|
(-)-beta-Elemenal
/ (-)-Elema-1,3,11(13)-trien-12-al |
No. 1400 |
|
|||||
|
C00010843
|
Macropone
|
CHEMBL353354
|
1 / 4 / 2 | No. 3751 | No. 35 |
|
||
|
C00012048
|
Occidiol
/ Occidenol |
No. 4166 |
|
|||||
|
C00021879
|
Mayurone
|
No. 4724 |
|
|||||
|
C00011009
|
beta-Dolabrin
|
C410956
|
No. 4728 |
|
||||
|
C00010311
|
(S)-Citronellic acid
/ (S)-3,7-Dimethyl-6-octenoic acid |
No. 8694 |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00002597 C00002608 C00007208 | 0 / 1 |
| Q99700 | Ataxin-2 | Unclassified protein | C00002597 C00007208 | 1 / 1 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00002597 C00007208 | 0 / 0 |
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00002597 C00007208 | 1 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00002597 C00007208 | 2 / 0 |
| O75496 | Geminin | Unclassified protein | C00002597 C00007208 | 0 / 0 |
| P14679 | Tyrosinase | Oxidoreductase | C00010843 | 4 / 2 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00002597 | 0 / 0 |
| P08253 | 72 kDa type IV collagenase | M10A | C00009089 | 1 / 3 |
| P02545 | Prelamin-A/C | Unclassified protein | C00007208 | 11 / 10 |
| Q9UNA4 | DNA polymerase iota | Enzyme | C00007208 | 0 / 0 |
| P14780 | Matrix metalloproteinase-9 | M10A | C00009089 | 2 / 2 |
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00002608 | 1 / 0 |
| Q06710 | Paired box protein Pax-8 | Unclassified protein | C00007208 | 1 / 2 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #103470 | Albinism, ocular, with sensorineural deafness |
P14679
|
| #203100 | Albinism, oculocutaneous, type ia; oca1a |
P14679
|
| #606952 | Albinism, oculocutaneous, type ib; oca1b |
P14679
|
| #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
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #137800 | Glioma susceptibility 1; glm1 |
O75874
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
| #603932 | Intervertebral disc disease; idd |
P14780
|
| #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
|
| #613073 | Metaphyseal anadysplasia 2; mandp2 |
P14780
|
| #259600 | Multicentric osteolysis, nodulosis, and arthropathy; mona |
P08253
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| #601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| 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)
|
| H00025 | Penile cancer |
P08253
(related)
P14780 (related) |
| H00028 | Choriocarcinoma |
P08253
(related)
|
| H00472 | Torg-Winchester syndrome |
P08253
(related)
|
| H00036 | Osteosarcoma |
P08684
(marker)
|
| H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
| H00038 | Malignant melanoma |
P14679
(marker)
|
| H00479 | Metaphyseal dysplasias |
P14780
(related)
|
| H00032 | Thyroid cancer |
Q06710
(related)
|
| H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
Q06710
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|