| class name | count |
|---|---|
| asterids | 5 |
| Spermatophyta | 1 |
| class name | count |
|---|---|
| Asteraceae | 4 |
| Cupressaceae | 1 |
| Apiaceae | 1 |
| br08003 Category | # of metabolite |
|---|---|
| Eudesmanes | 1 |
| br08003 Category | KEGG ID | KNApSAcK ID |
|---|---|---|
| Eudesmanes | C09450 | C00003283 |
| KNApSAcK ID | name | ChEMBL link | CTD link |
# of proteins in
ChEMBL interaction / related OMIM / related KEGG DISEASE |
# of genes in
CTD interaction / related diseases |
figure |
|---|---|---|---|---|---|---|
|
C00003283
|
Farinosin
|
CHEMBL1439902
|
15 / 16 / 15 |
|
||
|
C00012877
|
Callitrisin
/ [3R-(3alpha,3aalpha,4abeta,8aalpha,9aalpha)]-3a,4,4a,5,6,8a,9,9a-Octahydro-3,8a-dimethyl-5-methylenenaphtho[2,3-b]furan-2(3H)-one |
|
||||
|
C00012944
|
Virginin
/ [3S-(3alpha,3abeta,4abeta,8aalpha,9abeta)]-3a,4a,5,8a,9,9a-Hexahydro-3,8a-dimethyl-5-methylenenaphtho[2,3-b]furan-2,6(3H,4H)-dione |
|
||||
|
C00013030
|
Feropodin
/ [3S-(3alpha,3aalpha,5abeta,9aalpha,9bbeta)]-3a,4,5,5a,9a,9b-hexahydro-3,5a,9-trimethylnaphtho[1,2-b]furan-2(3H)-one |
|
||||
|
C00013077
|
Alloisosantonin
/ [3S-(3alpha,3aalpha,5abeta,9aalpha,9bbeta)]-3a,5,5a,9,9a,9b-hexahydro-3,5a-dimethyl-9-methylenenaphtho[1,2-b]furan-2,8(3H,4H)-dione |
|
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| Q99700 | Ataxin-2 | Unclassified protein | C00003283 | 1 / 1 |
| P11473 | Vitamin D3 receptor | NR1I1 | C00003283 | 2 / 3 |
| P42858 | Huntingtin | Unclassified protein | C00003283 | 1 / 1 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00003283 | 2 / 0 |
| O75496 | Geminin | Unclassified protein | C00003283 | 0 / 0 |
| P51151 | Ras-related protein Rab-9A | Unclassified protein | C00003283 | 0 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00003283 | 0 / 0 |
| Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00003283 | 1 / 2 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00003283 | 0 / 0 |
| Q9HC16 | DNA dC->dU-editing enzyme APOBEC-3G | Enzyme | C00003283 | 0 / 0 |
| O15118 | Niemann-Pick C1 protein | Unclassified protein | C00003283 | 1 / 1 |
| O75030 | Microphthalmia-associated transcription factor | Unclassified protein | C00003283 | 4 / 4 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00003283 | 0 / 0 |
| P10636 | Microtubule-associated protein tau | Unclassified protein | C00003283 | 4 / 3 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00003283 | 0 / 0 |
| OMIM | preferred title | UniProt |
|---|---|---|
| #103470 | Albinism, ocular, with sensorineural deafness |
O75030
|
| #114500 | Colorectal cancer; crc |
P84022
|
| #600274 | Frontotemporal dementia; ftd |
P10636
|
| #605130 | Hairy elbows, short stature, facial dysmorphism, and developmental delay |
Q03164
|
| #143100 | Huntington disease; hd |
P42858
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #614456 | Melanoma, cutaneous malignant, susceptibility to, 8; cmm8 |
O75030
|
| #607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
| #257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
| #260540 | Parkinson-dementia syndrome |
P10636
|
| #172700 | Pick disease of brain |
P10636
|
| #183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
| #601104 | Supranuclear palsy, progressive, 1; psnp1 |
P10636
|
| #103500 | Tietz syndrome |
O75030
|
| #277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
| #193510 | Waardenburg syndrome, type 2a; ws2a |
O75030
|
| KEGG | name | UniProt |
|---|---|---|
| H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
| H00038 | Malignant melanoma |
O75030
(related)
O75030 (marker) |
| H00169 | Ocular albinism |
O75030
(related)
|
| H00759 | Waardenburg syndrome (WS) |
O75030
(related)
|
| H01187 | Tietz syndrome |
O75030
(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)
|
| H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q03164
(related)
Q03164 (marker) |
| H00002 | Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) |
Q03164
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|