Species

KNApSAcK Entry

Organism name Calotropis gigantea
Genus Calotropis
Family Apocynaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Calotropis gigantea
Linked NCBI taxonomy ID 4066
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

Natural Activity

List (23)

Species Activity
Calotropis gigantea (L.) W. T. Aiton Alexeteric
Calotropis gigantea (L.) W. T. Aiton Alterative
Calotropis gigantea (L.) W. T. Aiton Analgesic
Calotropis gigantea (L.) W. T. Aiton Antiinflammatory
Calotropis gigantea (L.) W. T. Aiton Antispasmodic
Calotropis gigantea (L.) W. T. Aiton Antitumor
Calotropis gigantea (L.) W. T. Aiton Bitter
Calotropis gigantea (L.) W. T. Aiton Cardiotonic
Calotropis gigantea (L.) W. T. Aiton Depilatory
Calotropis gigantea (L.) W. T. Aiton Diaphoretic
Calotropis gigantea (L.) W. T. Aiton Digestive
Calotropis gigantea (L.) W. T. Aiton Emetic
Calotropis gigantea (L.) W. T. Aiton Expectorant
Calotropis gigantea (L.) W. T. Aiton Gastrotonic
Calotropis gigantea (L.) W. T. Aiton Laxative
Calotropis gigantea (L.) W. T. Aiton Nervine
Calotropis gigantea (L.) W. T. Aiton Proteolytic
Calotropis gigantea (L.) W. T. Aiton Rubefacient
Calotropis gigantea (L.) W. T. Aiton Stimulant
Calotropis gigantea (L.) W. T. Aiton Stomachic
Calotropis gigantea (L.) W. T. Aiton Tonic
Calotropis gigantea (L.) W. T. Aiton Uterotonic
Calotropis gigantea (L.) W. T. Aiton Vermifuge

Metabolite list (10)

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
C00005548 External link 512 Narcissin
/ Isorhamnetin 3-O-rutinoside
CHEMBL84174
CHEMBL258394
CHEMBL1711509
CHEMBL2165403
C031062
7 / 1 / 2 No. 1 No. 15
C00005572 External link 512 Calotropiside
/ Isorhamnetin 3-(2G-galactosylrutinoside)
/ Isorhamnetin 3-galactosyl-(1->2)-[rhamnosyl-(1->6)-glucoside]
/ Quercetin 3'-methyl ether 3-galactosyl-(1->2)-[rhamnosyl-(1->6)-glucoside]
/ 3-[(O-6-Deoxy-alpha-L-mannopyranosyl-(1->6)-O-[beta-D-galactopyranosyl-(1->2)]-beta-D-glucopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-1-benzopyran-4-one
No. 5 No. 15
C00022684 External link 512 Saussurol acetate
/ Taraxasteryl acetate
CHEMBL1796000
C092740
No. 23 No. 51
C00003738 External link 512 beta-Amyrin
/ beta-Amirin
/ beta-Amyrine
/ beta-Amyrenol
C036380
0 / 4 No. 23 No. 51
C00003737 External link 512 alpha-Amyrin
/ alpha-Amyrine
/ alpha-Amyrenol
No. 23 No. 51
C00003608 External link 512 Calactin
CHEMBL502127
CHEMBL495949
CHEMBL1992249
No. 468 No. 56
C00003609 External link 512 Calotropin
CHEMBL502127
CHEMBL495949
CHEMBL1992249
No. 468 No. 56
C00041405 External link 512 Calactinic acid methyl ester
CHEMBL499114
No. 468 No. 56
C00041246 External link 512 15beta-Hydroxycalotropin
CHEMBL448177
CHEMBL505598
No. 468 No. 56
C00032469 External link 512 Uzarigenin
CHEMBL21214
CHEMBL1453
CHEMBL1591205
33 / 41 / 58 No. 822 No. 56

Human Protein / Gene in interactions

36 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00005548 C00032469 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00005548 C00032469 0 / 1
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00005548 C00032469 0 / 0
O75496 Geminin Unclassified protein C00005548 C00032469 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00032469 1 / 0
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
P07237 Protein disulfide-isomerase Enzyme C00005548 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00032469 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00032469 2 / 0
Q16637 Survival motor neuron protein Unclassified protein C00032469 4 / 1
P51151 Ras-related protein Rab-9A Unclassified protein C00032469 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00032469 7 / 37
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
Q99700 Ataxin-2 Unclassified protein C00032469 1 / 1
P03372 Estrogen receptor NR3A1 C00005548 1 / 1
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00032469 1 / 1
P22310 UDP-glucuronosyltransferase 1-4 Enzyme C00032469 3 / 0
Q9UNA4 DNA polymerase iota Enzyme C00005548 0 / 0
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 (42)

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
#615363 Estrogen resistance; estrr P03372
#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)
H00026 Endometrial Cancer P03372 (marker)
P04637 (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)
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)

Diseases related to CTD interactions

4 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D005157 Facial Pain C00003738
D006930 Hyperalgesia C00003738
D007249 Inflammation C00003738
D010146 Pain C00003738