Organism name | Kadsura longipedunculata |
---|---|
Genus | Kadsura |
Family | Schisandraceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Kadsura longipedunculata |
---|---|
Linked NCBI taxonomy ID | 124782 |
Linked level | species |
Family in NCBI taxonomy | Schisandraceae |
---|---|
ID | 16733 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Magnoliophyta |
---|---|
ID | 3398 |
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 |
---|---|---|---|---|---|---|---|---|
C00002607 |
Grandisin
/ (-)-Grandisin |
CHEMBL459404
CHEMBL459405 CHEMBL1377609 CHEMBL2204392 |
C074346
|
4 / 3 / 7 | No. 38 | No. 21 | ||
C00024163 |
Fragransin B1
|
No. 38 | No. 21 | |||||
C00030688 |
Longipedunin B
|
No. 105 | No. 21 | |||||
C00002634 |
Wuweizisu C
/ (-)-Wuweizisu C |
CHEMBL437412
|
C031409
|
No. 105 | No. 21 | |||
C00029632 |
Acetyl-binankadsurin A
|
No. 105 | No. 21 | |||||
C00029829 |
Binankadsurin A
|
CHEMBL447240
CHEMBL518555 |
No. 105 | No. 21 | ||||
C00030689 |
Longipedunin C
|
No. 216 | No. 21 | |||||
C00030687 |
Longipedunin A
/ 1-Demethylkadsuphilin A |
CHEMBL526170
|
No. 216 | No. 21 | ||||
C00030517 |
Isoanwulignan
|
No. 282 | No. 21 | |||||
C00007215 |
Mesodihydroguaiaretic acid
|
CHEMBL430464
CHEMBL375927 CHEMBL1976696 |
16 / 18 / 12 | No. 282 | No. 21 | |||
C00030581 |
Kadsuralignan C
|
CHEMBL1812786
|
No. 406 | |||||
C00039531 |
Kadlongilactone A
/ (-)-Kadlongilactone A |
CHEMBL404848
CHEMBL401211 |
No. 556 | |||||
C00039646 |
Longipedlactone G
/ (-)-Longipedlactone G |
CHEMBL1077102
|
No. 556 | |||||
C00039645 |
Longipedlactone F
/ (-)-Longipedlactone F |
CHEMBL1087056
|
No. 556 | |||||
C00039647 |
Longipedlactone H
/ (-)-Longipedlactone H |
No. 556 | ||||||
C00039643 |
Longipedlactone D
/ (-)-Longipedlactone D |
CHEMBL1077100
|
No. 556 | |||||
C00039644 |
Longipedlactone E
/ (-)-Longipedlactone E |
No. 556 | ||||||
C00039532 |
Kadlongilactone B
/ (-)-Kadlongilactone B |
No. 556 | ||||||
C00039533 |
Kadlongilactone C
|
CHEMBL252749
CHEMBL399114 |
No. 556 | |||||
C00039534 |
Kadlongilactone D
|
No. 556 | ||||||
C00039535 |
Kadlongilactone E
/ (-)-Kadlongilactone E |
CHEMBL252749
CHEMBL399114 |
No. 556 | |||||
C00039640 |
Longipedlactone A
/ (-)-Longipedlactone A |
CHEMBL1086794
|
No. 556 | |||||
C00039641 |
Longipedlactone B
/ (-)-Longipedlactone B |
No. 556 | ||||||
C00039642 |
Longipedlactone C
/ (-)-Longipedlactone C |
No. 556 | ||||||
C00039648 |
Longipedlactone I
/ (-)-Longipedlactone I |
CHEMBL1077103
|
No. 556 | |||||
C00029437 |
2,7-dihydroxy-11,12-dehydrocalamenene
/ (-)-2,7-dihydroxy-11,12-dehydrocalamenene |
No. 824 | ||||||
C00030902 |
Otobaphenol
|
No. 1142 | No. 21 | |||||
C00002610 |
Kadsurin A
/ (+)-Kadsurin A |
CHEMBL37432
|
No. 2788 | No. 23 | ||||
C00030573 |
Kadlongirin A
|
No. 4869 | ||||||
C00030574 |
Kadlongirin B
|
No. 4869 |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
O75496 | Geminin | Unclassified protein | C00002607 C00007215 | 0 / 0 |
P00915 | Carbonic anhydrase 1 | Lyase | C00007215 | 0 / 0 |
P35218 | Carbonic anhydrase 5A, mitochondrial | Lyase | C00007215 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00007215 | 0 / 0 |
P37840 | Alpha-synuclein | Unclassified protein | C00007215 | 4 / 2 |
P00918 | Carbonic anhydrase 2 | Lyase | C00007215 | 1 / 2 |
P17405 | Sphingomyelin phosphodiesterase | Enzyme | C00007215 | 2 / 2 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00007215 | 2 / 0 |
Q99700 | Ataxin-2 | Unclassified protein | C00007215 | 1 / 1 |
Q9Y2D0 | Carbonic anhydrase 5B, mitochondrial | Lyase | C00007215 | 0 / 0 |
P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00007215 | 0 / 0 |
P63092 | Guanine nucleotide-binding protein G(s) subunit alpha isoforms short | Other membrane protein | C00007215 | 7 / 3 |
P04150 | Glucocorticoid receptor | NR3C1 | C00007215 | 0 / 1 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00002607 | 0 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00007215 | 0 / 0 |
Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00007215 | 0 / 0 |
O00255 | Menin | Unclassified protein | C00002607 | 2 / 5 |
Q03164 | Histone-lysine N-methyltransferase 2A | Enzyme | C00002607 | 1 / 2 |
Q13148 | TAR DNA-binding protein 43 | Unclassified protein | C00007215 | 1 / 1 |
OMIM | preferred title | UniProt |
---|---|---|
#219080 | Acth-independent macronodular adrenal hyperplasia; aimah |
P63092
|
#612069 | Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 |
Q13148
|
#114500 | Colorectal cancer; crc |
P84022
|
#127750 | Dementia, lewy body; dlb |
P37840
|
#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
|
#131100 | Multiple endocrine neoplasia, type i; men1 |
O00255
|
#257200 | Niemann-pick disease, type a |
P17405
|
#607616 | Niemann-pick disease, type b |
P17405
|
#166350 | Osseous heteroplasia, progressive; poh |
P63092
|
#259730 | Osteopetrosis, autosomal recessive 3; optb3 |
P00918
|
#168601 | Parkinson disease 1, autosomal dominant; park1 |
P37840
|
#605543 | Parkinson disease 4, autosomal dominant; park4 |
P37840
|
#168600 | Parkinson disease, late-onset; pd |
P37840
|
#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
|
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)
|
H00241 | Combined proximal and distal renal tubular acidosis (RTA type 3) |
P00918
(related)
|
H00436 | Osteopetrosis |
P00918
(related)
|
H00599 | 46,XX disorders of sex development (Disorders related to androgen excess) |
P04150
(related)
|
H00137 | Niemann-Pick disease (NPD) typeA and B |
P17405
(related)
|
H00424 | Defects in the degradation of sphingomyelin |
P17405
(related)
|
H00057 | Parkinson's disease (PD) |
P37840
(related)
|
H00066 | Lewy body dementia (LBD) |
P37840
(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)
|
H00058 | Amyotrophic lateral sclerosis (ALS) |
Q13148
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|