Organism name | Carthamus tinctorius |
---|---|
Genus | Carthamus |
Family | Asteraceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Carthamus tinctorius |
---|---|
Linked NCBI taxonomy ID | 4222 |
Linked level | species |
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 |
---|---|---|---|---|---|---|---|---|
C00005308
![]() |
6-Hydroxykaempferol 3,6-diglucoside
|
No. 1 | No. 15 |
![]() |
||||
C00005169
![]() |
Nicotiflorin
/ Nicotifloroside / Kaempferol 3-O-rutinoside / Kaempferol 3-O-(alpha-L-rhamnopyranosyl(1->6)-beta-D-glucopyranoside / (-)-Kaempferol 3-O-(alpha-L-rhamnopyranosyl(1->6)-beta-D-glucopyranoside |
CHEMBL431610
CHEMBL79790 CHEMBL255020 CHEMBL501550 CHEMBL498879 CHEMBL1419228 CHEMBL1875691 |
22 / 10 / 12 | No. 1 | No. 15 |
![]() |
||
C00005427
![]() |
Quercetin 3,7-diglucoside
/ Quercetin 3,7-O-beta-diglucopyranoside / Quercetin 3,7-di-O-beta-D-glucopyranoside |
CHEMBL1797051
|
No. 1 | No. 15 |
![]() |
|||
C00005138
![]() |
Astragalin
/ Kaempferol 3-glucoside / Kaempferol 3-O-beta-D-glucoside / Kaempferol 3-O-beta-D-glucopyranoside |
CHEMBL233930
CHEMBL453290 CHEMBL1572115 |
C001579
|
10 / 6 / 7 | 0 / 1 | No. 2 | No. 15 |
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C00013868
![]() |
Quercetin 7-(6''-acetylglucoside)
/ 7-[(6-O-Acetyl-beta-D-glucopyranosyl)oxy]-2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-4H-1-benzopyran-4-one |
No. 2 | No. 15 |
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||||
C00005306
![]() |
6-Hydroxykaempferol 3-glucoside
|
No. 2 | No. 15 |
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||||
C00001051
![]() |
6-Hydroxykaempferol
|
CHEMBL455504
|
No. 3 | No. 15 |
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|||
C00004593
![]() |
6-Methoxykaempferol
/ 3,5,7,4'-Tetrahydroxy-6-methoxyflavone / 3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-6-methoxy-4H-1-benzopyran-4-one |
CHEMBL462898
|
No. 3 | No. 15 |
![]() |
|||
C00005311
![]() |
6-Hydroxykaempferol 3,6,7-triglucoside
|
No. 5 | No. 15 |
![]() |
||||
C00005310
![]() |
6-Hydroxykaempferol 3-rutinoside-6-glucoside
|
No. 5 | No. 15 |
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||||
C00008231
![]() |
Carthamidin 5-glucoside
|
No. 12 | No. 14 |
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||||
C00000001
![]() |
GA1
/ Gibberellin A1 |
C422660
|
No. 40 | No. 41 |
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|||
C00000003
![]() |
GA3
/ Gibberellin A3 |
CHEMBL513241
CHEMBL566653 CHEMBL1232952 CHEMBL1476967 CHEMBL1487394 |
C007842
|
10 / 18 / 17 | No. 40 | No. 41 |
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|
C00000029
![]() |
GA29
/ Gibberellin A29 |
No. 40 | No. 41 |
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||||
C00000020
![]() |
GA20
/ Gibberellin A20 |
No. 40 | No. 41 |
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||||
C00014329
![]() |
5,6,7,4'-Tetrahydroxyflavanone 6,7-diglucoside
|
No. 48 | No. 14 |
![]() |
||||
C00001230
![]() |
Nervonic acid
|
C013147
|
No. 184 | No. 68 |
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|||
C00000019
![]() |
GA19
/ Gibberellin A19 |
C120175
|
No. 187 | No. 41 |
![]() |
|||
C00000606
![]() |
(-)-Matairesinol
|
CHEMBL425148
|
C068935
|
1 / 0 / 0 | No. 223 | No. 21 |
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|
C00006339
![]() |
Carthamin
|
C103141
|
No. 2732 |
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||||
C00006340
![]() |
Safflor yellow B
|
No. 2732 |
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|||||
C00014588
![]() |
Anhydrosafflor yellow B
|
No. 2732 |
![]() |
|||||
C00014589
![]() |
Precarthamin
|
No. 2732 |
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|||||
C00014590
![]() |
Tinctormine
|
No. 3392 |
![]() |
|||||
C00006246
![]() |
Safflor yellow A
|
No. 3392 |
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|||||
C00001292
![]() |
Safynol
|
No. 4550 |
![]() |
|||||
C00001281
![]() |
Dehydrosafynol
|
No. 4550 |
![]() |
|||||
C00046653
![]() |
Cartorimine
/ (-)-Cartorimine |
No. 5821 |
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|||||
C00029911
![]() |
Carthamoside A1
/ (-)-Carthamoside A1 / 4',6'-Acetonide-8Z-decane-4,6-diyne-1-O-beta-D-glucopyranoside |
No. 6395 |
![]() |
|||||
C00006418
![]() |
Safflomin C
|
No. 7435 |
![]() |
|||||
C00002372
![]() |
Carthamone
|
No. 8443 | No. 13 |
![]() |
accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
---|---|---|---|---|
Q99700 | Ataxin-2 | Unclassified protein | C00005138 C00005169 | 1 / 1 |
P27695 | DNA-(apurinic or apyrimidinic site) lyase | Enzyme | C00005138 C00005169 | 0 / 0 |
Q9UNA4 | DNA polymerase iota | Enzyme | C00005138 C00005169 | 0 / 0 |
Q9Y253 | DNA polymerase eta | Enzyme | C00005138 C00005169 | 1 / 1 |
O75496 | Geminin | Unclassified protein | C00000003 C00005169 | 0 / 0 |
Q13526 | Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 | Enzyme | C00005138 C00005169 | 0 / 0 |
P07237 | Protein disulfide-isomerase | Enzyme | C00005138 C00005169 | 0 / 0 |
Q9Y468 | Lethal(3)malignant brain tumor-like protein 1 | Unclassified protein | C00005169 | 0 / 0 |
P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00000003 | 0 / 1 |
P02545 | Prelamin-A/C | Unclassified protein | C00000003 | 11 / 10 |
Q9NR56 | Muscleblind-like protein 1 | Unclassified protein | C00005169 | 1 / 0 |
P11473 | Vitamin D3 receptor | NR1I1 | C00005169 | 2 / 3 |
P04278 | Sex hormone-binding globulin | Secreted protein | C00000606 | 0 / 0 |
P39748 | Flap endonuclease 1 | Enzyme | C00005169 | 0 / 0 |
P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00000003 | 2 / 0 |
P10253 | Lysosomal alpha-glucosidase | Hydrolase | C00005169 | 1 / 1 |
P15121 | Aldose reductase | Enzyme | C00005138 | 0 / 0 |
P06746 | DNA polymerase beta | Enzyme | C00005169 | 0 / 0 |
P47989 | Xanthine dehydrogenase/oxidase | Oxidoreductase | C00005169 | 1 / 1 |
P83916 | Chromobox protein homolog 1 | Unclassified protein | C00000003 | 0 / 0 |
P14679 | Tyrosinase | Oxidoreductase | C00005138 | 4 / 2 |
P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00000003 | 0 / 0 |
Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00005138 | 0 / 0 |
P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00000003 | 1 / 1 |
P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00000003 | 0 / 1 |
P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00000003 | 1 / 0 |
O75164 | Lysine-specific demethylase 4A | Enzyme | C00005169 | 0 / 0 |
Q9UIF8 | Bromodomain adjacent to zinc finger domain protein 2B | Unclassified protein | C00005169 | 0 / 0 |
P10275 | Androgen receptor | NR3C4 | C00000003 | 3 / 4 |
Q9UBT6 | DNA polymerase kappa | Enzyme | C00005169 | 0 / 0 |
P46063 | ATP-dependent DNA helicase Q1 | Enzyme | C00005169 | 0 / 0 |
Q13951 | Core-binding factor subunit beta | Unclassified protein | C00005169 | 0 / 1 |
Q01196 | Runt-related transcription factor 1 | Unclassified protein | C00005169 | 1 / 4 |
O94925 | Glutaminase kidney isoform, mitochondrial | Enzyme | C00005169 | 0 / 0 |
P01215 | Glycoprotein hormones alpha chain | Unclassified protein | C00005138 | 0 / 3 |
Q14191 | Werner syndrome ATP-dependent helicase | Enzyme | C00005169 | 2 / 1 |
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
|
#300068 | Androgen insensitivity syndrome; ais |
P10275
|
#312300 | Androgen insensitivity, partial; pais |
P10275
|
#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
Q14191 |
#609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
#608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
#181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
#232300 | Glycogen storage disease ii |
P10253
|
#610140 | Heart-hand syndrome, slovenian type |
P02545
|
#176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
#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
|
#613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
#159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
#607948 | Mycobacterium tuberculosis, susceptibility to |
P11473
|
#160900 | Myotonic dystrophy 1; dm1 |
Q9NR56
|
#601399 | Platelet disorder, familial, with associated myeloid malignancy |
Q01196
|
#275210 | Restrictive dermopathy, lethal |
P02545
|
#601800 | Skin/hair/eye pigmentation, variation in, 3; shep3 |
P14679
|
#313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
#183090 | Spinocerebellar ataxia 2; sca2 |
Q99700
|
#277440 | Vitamin d-dependent rickets, type 2a; vddr2a |
P11473
|
#277700 | Werner syndrome; wrn |
Q14191
|
#278300 | Xanthinuria, type i |
P47989
|
#278750 | Xeroderma pigmentosum, variant type; xpv |
Q9Y253
|
KEGG | name | UniProt |
---|---|---|
H00081 | Hashimoto's thyroiditis |
P01215
(marker)
|
H00082 | Graves' disease |
P01215
(marker)
|
H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P01215
(marker)
|
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)
|
H00036 | Osteosarcoma |
P08684
(marker)
|
H00069 | Glycogen storage diseases (GSD) |
P10253
(related)
|
H00024 | Prostate cancer |
P10275
(related)
|
H00062 | Spinal and bulbar muscular atrophy (SBMA) |
P10275
(related)
|
H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) |
P10275
(related)
|
H00609 | 46,XY disorders of sex development (Other) |
P10275
(related)
|
H00342 | Tuberculosis |
P11473
(related)
|
H00784 | Localized autosomal recessive hypotrichosis |
P11473
(related)
|
H01143 | Vitamin D-dependent rickets |
P11473
(related)
|
H01205 | Coumarin resistance |
P11712
(related)
|
H00168 | Oculocutaneous albinism (OCA) |
P14679
(related)
|
H00038 | Malignant melanoma |
P14679
(marker)
|
H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
H00192 | Xanthinuria |
P47989
(related)
|
H00001 | Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) |
Q01196
(related)
Q01196 (marker) |
H00003 | Acute myeloid leukemia (AML) |
Q01196
(related)
Q01196 (marker) Q13951 (marker) |
H00004 | Chronic myeloid leukemia (CML) |
Q01196
(related)
|
H00978 | Thrombocytopenia (THC) |
Q01196
(related)
|
H00296 | Defects in RecQ helicases |
Q14191
(related)
|
H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|
H00403 | Disorders of nucleotide excision repair |
Q9Y253
(related)
|