Asclepias curassavica L.
Species
KNApSAcK Entry
| Organism name | Asclepias curassavica L. |
|---|---|
| Genus | Asclepias |
| Family | Apocynaceae |
| Kingdom | Plantae |
NCBI taxonomy
Entry
| Linked NCBI taxonomy name | Asclepias curassavica |
|---|---|
| Linked NCBI taxonomy ID | 52823 |
| Linked level | species |
Family
| Family in NCBI taxonomy | Apocynaceae |
|---|---|
| ID | 4056 |
Kingdom (Superkingdom)
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
Plant class
| Plant class | asterids |
|---|---|
| ID | 71274 |
Metabolite list (16)
| 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 |
|---|---|---|---|---|---|---|---|---|
C00002631
|
(+)-Lirioresinol B
/ (+)-Syringaresinol |
CHEMBL361362
CHEMBL402653 |
C042192
|
1 / 0 / 0 | No. 38 | No. 21 |
|
|
|
C00030416
|
Gofruside
|
CHEMBL1169679
|
No. 109 | No. 56 |
|
|||
|
C00029403
|
16alpha-Acetoxycalactin
|
CHEMBL448662
|
No. 468 | No. 56 |
|
|||
|
C00003640
|
Uscharidin
|
CHEMBL449207
|
No. 468 | No. 56 |
|
|||
|
C00029402
|
16alpha-Acetoxyasclepin
|
CHEMBL454779
|
No. 468 | No. 56 |
|
|||
|
C00003609
|
Calotropin
|
CHEMBL502127
CHEMBL495949 CHEMBL1992249 |
No. 468 | No. 56 |
|
|||
|
C00029404
|
16alpha-Acetoxycalotropin
|
CHEMBL448662
|
No. 468 | No. 56 |
|
|||
|
C00029405
|
16alpha-Hydroxyasclepin
|
CHEMBL471686
|
No. 468 | No. 56 |
|
|||
|
C00003603
|
Asclepin
|
CHEMBL445086
|
C020214
|
No. 468 | No. 56 |
|
||
|
C00029413
|
19-nor-16alpha-Acetoxy-10beta-hydroxyasclepin
|
No. 468 | No. 56 |
|
||||
|
C00032466
|
Uscharin
|
CHEMBL500585
|
No. 468 | No. 56 |
|
|||
|
C00029406
|
16alpha-Hydroxyuscharin
|
No. 468 | No. 56 |
|
||||
|
C00030013
|
Coroglaucigenin
|
CHEMBL495179
|
No. 822 | No. 56 |
|
|||
|
C00032536
|
Xysmalogenin
/ 5,6-Dehydrouzarigenin |
No. 822 | No. 56 |
|
||||
|
C00032469
|
Uzarigenin
|
CHEMBL21214
CHEMBL1453 CHEMBL1591205 |
33 / 41 / 58 | No. 822 | No. 56 |
|
||
|
C00029581
|
6'-O-(E-4-Hydroxycinnamoyl)-desglucouzarin
|
No. 6593 |
|
Human Protein / Gene in interactions
34 ChEMBL Protein in interactions
| accession | description | class description | KNApSAcK metabolite in interactions |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|
| P10635 | Cytochrome P450 2D6 | Cytochrome P450 2D6 | C00032469 | 1 / 0 |
| P22310 | UDP-glucuronosyltransferase 1-4 | Enzyme | C00032469 | 3 / 0 |
| P04637 | Cellular tumor antigen p53 | Transcription Factor | C00032469 | 7 / 37 |
| Q16637 | Survival motor neuron protein | Unclassified protein | C00032469 | 4 / 1 |
| Q99700 | Ataxin-2 | Unclassified protein | C00032469 | 1 / 1 |
| P02545 | Prelamin-A/C | Unclassified protein | C00032469 | 11 / 10 |
| P16473 | Thyrotropin receptor | Glycohormone receptor | C00032469 | 3 / 2 |
| P11712 | Cytochrome P450 2C9 | Cytochrome P450 2C9 | C00032469 | 0 / 1 |
| P11387 | DNA topoisomerase 1 | Isomerase | C00002631 | 0 / 0 |
| Q16665 | Hypoxia-inducible factor 1-alpha | Transcription Factor | C00032469 | 0 / 0 |
| P84022 | Mothers against decapentaplegic homolog 3 | Unclassified protein | C00032469 | 2 / 0 |
| O75496 | Geminin | Unclassified protein | C00032469 | 0 / 0 |
| P51151 | Ras-related protein Rab-9A | Unclassified protein | C00032469 | 0 / 0 |
| P43220 | Glucagon-like peptide 1 receptor | Glucagon-like peptide receptor | C00032469 | 0 / 0 |
| P54707 | Potassium-transporting ATPase alpha chain 2 | Potassium-transporting P-type ATPase alpha subunit | C00032469 | 0 / 0 |
| P83916 | Chromobox protein homolog 1 | Unclassified protein | C00032469 | 0 / 0 |
| P05177 | Cytochrome P450 1A2 | Cytochrome P450 1A2 | C00032469 | 0 / 0 |
| O15118 | Niemann-Pick C1 protein | Unclassified protein | C00032469 | 1 / 1 |
| Q96QE3 | ATPase family AAA domain-containing protein 5 | Unclassified protein | C00032469 | 0 / 0 |
| P33261 | Cytochrome P450 2C19 | Cytochrome P450 2C19 | C00032469 | 1 / 1 |
| P08684 | Cytochrome P450 3A4 | Cytochrome P450 3A4 | C00032469 | 0 / 1 |
| Q16236 | Nuclear factor erythroid 2-related factor 2 | Unclassified protein | C00032469 | 0 / 0 |
| Q96KQ7 | Histone-lysine N-methyltransferase EHMT2 | Enzyme | C00032469 | 0 / 0 |
| O75874 | Isocitrate dehydrogenase [NADP] cytoplasmic | Enzyme | C00032469 | 1 / 0 |
| Q6ZQN7 | Solute carrier organic anion transporter family member 4C1 | Unclassified protein | C00032469 | 0 / 0 |
| P05023 | Sodium/potassium-transporting ATPase subunit alpha-1 | Hydrolase | C00032469 | 0 / 0 |
| P14415 | Sodium/potassium-transporting ATPase subunit beta-2 | potassium_sodium | C00032469 | 0 / 0 |
| P13637 | Sodium/potassium-transporting ATPase subunit alpha-3 | Hydrolase | C00032469 | 2 / 1 |
| Q13733 | Sodium/potassium-transporting ATPase subunit alpha-4 | Hydrolase | C00032469 | 0 / 0 |
| P54710 | Sodium/potassium-transporting ATPase subunit gamma | potassium_sodium | C00032469 | 1 / 1 |
| P54709 | Sodium/potassium-transporting ATPase subunit beta-3 | potassium_sodium | C00032469 | 0 / 0 |
| P50993 | Sodium/potassium-transporting ATPase subunit alpha-2 | Hydrolase | C00032469 | 2 / 2 |
| P05026 | Sodium/potassium-transporting ATPase subunit beta-1 | potassium_sodium | C00032469 | 0 / 0 |
| Q06710 | Paired box protein Pax-8 | Unclassified protein | C00032469 | 1 / 2 |
Related Diseases
Diseases related to proteins in ChEMBL interactions
OMIM (41)
| OMIM | preferred title | UniProt |
|---|---|---|
| #202300 | Adrenocortical carcinoma, hereditary; adcc |
P04637
|
| #104290 | Alternating hemiplegia of childhood 1; ahc1 |
P50993
|
| #614820 | Alternating hemiplegia of childhood 2; ahc2 |
P13637
|
| #614740 | Basal cell carcinoma, susceptibility to, 7; bcc7 |
P04637
|
| #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
|
| #218800 | Crigler-najjar syndrome, type i |
P22310
|
| #606785 | Crigler-najjar syndrome, type ii |
P22310
|
| #609535 | Drug metabolism, poor, cyp2c19-related |
P33261
|
| #608902 | Drug metabolism, poor, cyp2d6-related |
P10635
|
| #128235 | Dystonia 12; dyt12 |
P13637
|
| #181350 | Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 |
P02545
|
| #133239 | Esophageal cancer |
P04637
|
| #143500 | Gilbert syndrome |
P22310
|
| #137800 | Glioma susceptibility 1; glm1 |
O75874
|
| #610140 | Heart-hand syndrome, slovenian type |
P02545
|
| #176670 | Hutchinson-gilford progeria syndrome; hgps |
P02545
|
| #603373 | Hyperthyroidism, familial gestational |
P16473
|
| #609152 | Hyperthyroidism, nonautoimmune |
P16473
|
| #154020 | Hypomagnesemia 2, renal; homg2 |
P54710
|
| #275200 | Hypothyroidism, congenital, nongoitrous, 1; chng1 |
P16473
|
| #218700 | Hypothyroidism, congenital, nongoitrous, 2; chng2 |
Q06710
|
| #151623 | Li-fraumeni syndrome 1; lfs1 |
P04637
|
| #151660 | Lipodystrophy, familial partial, type 2; fpld2 |
P02545
|
| #613795 | Loeys-dietz syndrome, type 3; lds3 |
P84022
|
| #211980 | Lung cancer |
P04637
|
| #248370 | Mandibuloacral dysplasia with type a lipodystrophy; mada |
P02545
|
| #602481 | Migraine, familial hemiplegic, 2; fhm2 |
P50993
|
| #613205 | Muscular dystrophy, congenital, lmna-related |
P02545
|
| #159001 | Muscular dystrophy, limb-girdle, type 1b; lgmd1b |
P02545
|
| #257220 | Niemann-pick disease, type c1; npc1 |
O15118
|
| #260500 | Papilloma of choroid plexus; cpp |
P04637
|
| #275210 | Restrictive dermopathy, lethal |
P02545
|
| #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
|
| #275355 | Squamous cell carcinoma, head and neck; hnscc |
P04637
|
KEGG DISEASE (58)
| KEGG | name | UniProt |
|---|---|---|
| H00136 | Niemann-Pick disease type C (NPC) |
O15118
(related)
|
| 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)
|
| H00004 | Chronic myeloid leukemia (CML) |
P04637
(related)
|
| H00005 | Chronic lymphocytic leukemia (CLL) |
P04637
(related)
|
| H00006 | Hairy-cell leukemia |
P04637
(related)
|
| H00008 | Burkitt lymphoma |
P04637
(related)
|
| H00009 | Adult T-cell leukemia |
P04637
(related)
|
| H00010 | Multiple myeloma |
P04637
(related)
|
| H00013 | Small cell lung cancer |
P04637
(related)
|
| H00014 | Non-small cell lung cancer |
P04637
(related)
|
| H00015 | Malignant pleural mesothelioma |
P04637
(related)
|
| H00016 | Oral cancer |
P04637
(related)
P04637 (marker) |
| H00017 | Esophageal cancer |
P04637
(related)
P04637 (marker) |
| H00018 | Gastric cancer |
P04637
(related)
|
| H00019 | Pancreatic cancer |
P04637
(related)
P04637 (marker) |
| H00020 | Colorectal cancer |
P04637
(related)
P04637 (marker) |
| H00022 | Bladder cancer |
P04637
(related)
|
| H00025 | Penile cancer |
P04637
(related)
P04637 (marker) |
| H00026 | Endometrial Cancer |
P04637
(related)
|
| H00027 | Ovarian cancer |
P04637
(related)
|
| H00028 | Choriocarcinoma |
P04637
(related)
|
| H00029 | Vulvar cancer |
P04637
(related)
|
| H00031 | Breast cancer |
P04637
(related)
|
| H00032 | Thyroid cancer |
P04637
(related)
Q06710 (related) |
| H00033 | Adrenal carcinoma |
P04637
(related)
|
| H00036 | Osteosarcoma |
P04637
(related)
P08684 (marker) |
| H00038 | Malignant melanoma |
P04637
(related)
|
| H00039 | Basal cell carcinoma |
P04637
(related)
|
| H00040 | Squamous cell carcinoma |
P04637
(related)
|
| H00041 | Kaposi's sarcoma |
P04637
(related)
|
| H00042 | Glioma |
P04637
(related)
P04637 (marker) |
| H00044 | Cancer of the anal canal |
P04637
(related)
|
| H00046 | Cholangiocarcinoma |
P04637
(related)
|
| H00047 | Gallbladder cancer |
P04637
(related)
|
| H00048 | Hepatocellular carcinoma |
P04637
(related)
|
| H00055 | Laryngeal cancer |
P04637
(related)
P04637 (marker) |
| H00881 | Li-Fraumeni syndrome |
P04637
(related)
|
| H01007 | Choroid plexus papilloma |
P04637
(related)
|
| H00021 | Renal cell carcinoma |
P04637
(marker)
|
| H01205 | Coumarin resistance |
P11712
(related)
|
| H00831 | Primary dystonia |
P13637
(related)
|
| H00250 | Congenital nongoitrous hypothyroidism (CHNG) |
P16473
(related)
Q06710 (related) |
| H01269 | Congenital hyperthyroidism |
P16473
(related)
|
| H01171 | Poor drug metabolism (PM) |
P33261
(related)
|
| H00775 | Familial or sporadic hemiplegic migraine |
P50993
(related)
|
| H00998 | Alternating hemiplegia of childhood |
P50993
(related)
|
| H01210 | Hypomagnesemia |
P54710
(related)
|
| H00455 | Spinal muscular atrophy (SMA) |
Q16637
(related)
|
| H00063 | Spinocerebellar ataxia (SCA) |
Q99700
(related)
|