Species

KNApSAcK Entry

Organism name Piper longum
Genus Piper
Family Piperaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Piper longum
Linked NCBI taxonomy ID 49511
Linked level species

Family

Family in NCBI taxonomy Piperaceae
ID 16739

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Magnoliophyta
ID 3398

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
C00007195 External link 512 (+)-Fargesin
CHEMBL462822
C058339
No. 38 No. 21
C00027470 External link 512 Piperolactam A
CHEMBL387864
C457227
No. 125
C00000601 External link 512 (+)-Sesamin
CHEMBL43469
CHEMBL252915
CHEMBL1572261
CHEMBL1591714
CHEMBL1708854
CHEMBL1904496
CHEMBL1968861
C054125
20 / 24 / 15 0 / 5 No. 621 No. 21
C00034654 External link 512 Retrofractamide A
No. 638
C00030436 External link 512 Guineensine
No. 638
C00002663 External link 512 2-Phenylethanol
/ Phenethyl alcohol
/ Phenylethyl alcohol
/ beta-Phenethyl alcohol
CHEMBL448500
D010626
2 / 1 / 1 No. 885
C00002066 External link 512 Piplartine
/ Piperlongumine
CHEMBL465843
CHEMBL1456697
28 / 44 / 65 No. 1640 No. 1
C00028813 External link 512 Pellitorine
C008778
No. 1863
C00003204 External link 512 l-Zingiberene
/ (-)-Zingiberene
/ alpha-Zingiberene
CHEMBL479020
No. 2380 No. 38
C00002065 External link 512 Piperine
/ Bioperine
/ 1-Piperoylpiperidine
CHEMBL43185
CHEMBL1395862
32 / 47 / 64 No. 4209 No. 1

Human Protein / Gene in interactions

47 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000601 C00002065 C00002066 1 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00000601 C00002065 C00002066 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00000601 C00002065 C00002066 4 / 1
O75496 Geminin Unclassified protein C00000601 C00002066 C00002663 0 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00000601 C00002065 C00002066 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000601 C00002065 C00002066 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000601 C00002065 C00002066 0 / 1
Q9UNA4 DNA polymerase iota Enzyme C00000601 C00002065 C00002066 0 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000601 C00002065 C00002066 0 / 1
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein C00000601 C00002065 C00002066 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000601 C00002066 4 / 3
P11473 Vitamin D3 receptor NR1I1 C00000601 C00002066 2 / 3
P02545 Prelamin-A/C Unclassified protein C00002065 C00002066 11 / 10
P00352 Retinal dehydrogenase 1 Enzyme C00002065 C00002066 0 / 0
O15118 Niemann-Pick C1 protein Unclassified protein C00002065 C00002066 1 / 1
P15428 15-hydroxyprostaglandin dehydrogenase [NAD(+)] Enzyme C00000601 C00002065 2 / 2
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00000601 C00002066 2 / 0
Q99700 Ataxin-2 Unclassified protein C00002065 C00002066 1 / 1
P51151 Ras-related protein Rab-9A Unclassified protein C00002065 C00002066 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002065 C00002066 3 / 3
P43220 Glucagon-like peptide 1 receptor Glucagon-like peptide receptor C00000601 C00002066 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002065 C00002066 0 / 0
P04637 Cellular tumor antigen p53 Transcription Factor C00002065 C00002066 7 / 37
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00000601 C00002065 0 / 0
Q13148 TAR DNA-binding protein 43 Unclassified protein C00000601 C00002066 1 / 1
P04150 Glucocorticoid receptor NR3C1 C00002065 0 / 1
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002065 5 / 3
Q8NER1 Transient receptor potential cation channel subfamily V member 1 TRPV (Vanilloid) C00002065 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00002065 0 / 0
P83916 Chromobox protein homolog 1 Unclassified protein C00000601 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00000601 7 / 3
P38398 Breast cancer type 1 susceptibility protein Enzyme C00002065 4 / 2
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00002066 0 / 0
P17405 Sphingomyelin phosphodiesterase Enzyme C00002065 2 / 2
O75030 Microphthalmia-associated transcription factor Unclassified protein C00002066 4 / 4
O15296 Arachidonate 15-lipoxygenase B Enzyme C00000601 0 / 0
P08183 Multidrug resistance protein 1 drug C00002065 1 / 0
P21397 Amine oxidase [flavin-containing] A Oxidoreductase C00002065 1 / 1
P19793 Retinoic acid receptor RXR-alpha NR2B1 C00002065 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00002065 3 / 2
P27338 Amine oxidase [flavin-containing] B Oxidoreductase C00002065 0 / 0
P35869 Aryl hydrocarbon receptor Transcription Factor C00002065 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00002065 0 / 0
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002663 1 / 1
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00002066 1 / 0
Q06710 Paired box protein Pax-8 Unclassified protein C00002066 1 / 2
Q9HC16 DNA dC->dU-editing enzyme APOBEC-3G Enzyme C00002066 0 / 0

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (69)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#103470 Albinism, ocular, with sensorineural deafness O75030
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
%606641 Body mass index; bmi P37231
#114480 Breast cancer P38398
#604370 Breast-ovarian cancer, familial, susceptibility to, 1; brovca1 P38398
#300615 Brunner syndrome P21397
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#609338 Carotid intimal medial thickness 1 P37231
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#114500 Colorectal cancer; crc P84022
#119900 Digital clubbing, isolated congenital P15428
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#133239 Esophageal cancer P04637
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
P37231
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#259100 Hypertrophic osteoarthropathy, primary, autosomal recessive, 1; phoar1 P15428
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#218700 Hypothyroidism, congenital, nongoitrous, 2; chng2 Q06710
#612244 Inflammatory bowel disease 13; ibd13 P08183
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#211980 Lung cancer P04637
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#174800 Mccune-albright syndrome; mas P63092
#614456 Melanoma, cutaneous malignant, susceptibility to, 8; cmm8 O75030
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#257200 Niemann-pick disease, type a P17405
#607616 Niemann-pick disease, type b P17405
#257220 Niemann-pick disease, type c1; npc1 O15118
#601665 Obesity P37231
#166350 Osseous heteroplasia, progressive; poh P63092
#167000 Ovarian cancer P38398
#614320 Pancreatic cancer, susceptibility to, 4; pnca4 P38398
#260500 Papilloma of choroid plexus; cpp P04637
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#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
#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
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#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 DISEASE (76)

KEGG name UniProt
H00136 Niemann-Pick disease type C (NPC) O15118 (related)
H00038 Malignant melanoma O75030 (related)
O75030 (marker)
P04637 (related)
H00169 Ocular albinism O75030 (related)
H00759 Waardenburg syndrome (WS) O75030 (related)
H01187 Tietz syndrome O75030 (related)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
P37231 (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)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (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)
P38398 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
P38398 (related)
H00032 Thyroid cancer P04637 (related)
P37231 (related)
Q06710 (related)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (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)
H01205 Coumarin resistance P11712 (related)
H00457 Primary hypertrophic osteoarthropathy (PHO) P15428 (related)
H01246 Isolated congenital nail clubbing (ICNC) P15428 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
Q06710 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H00137 Niemann-Pick disease (NPD) typeA and B P17405 (related)
H00424 Defects in the degradation of sphingomyelin P17405 (related)
H00548 Brunner syndrome P21397 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (related)
Q9NUW8 (related)
H00480 Non-syndromic X-linked mental retardation Q99714 (related)
H00658 Syndromic X-linked mental retardation Q99714 (related)
H00925 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency Q99714 (related)

Diseases related to CTD interactions

5 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D001930 Brain Injuries C00000601
D002375 Catalepsy C00000601
D018476 Hypokinesia C00000601
D020244 Infarction, Middle Cerebral Artery C00000601
D020734 Parkinsonian Disorders C00000601