Species

KNApSAcK Entry

Organism name Piper nigrum L.
Genus Piper
Family Piperaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Piper nigrum
Linked NCBI taxonomy ID 13216
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

Natural Activity

List (132)

Species Activity
Piper nigrum L. Abortifacient
Piper nigrum L. Alexeteric
Piper nigrum L. Analeptic
Piper nigrum L. Analgesic
Piper nigrum L. Antibacterial
Piper nigrum L. Anticonvulsant
Piper nigrum L. Antidote, fish
Piper nigrum L. Antidote, mushroom
Piper nigrum L. Antidote,shellfish
Piper nigrum L. Antiglucuronidase
Piper nigrum L. Antileishmanic
Piper nigrum L. Antioxidant
Piper nigrum L. Antipyretic
Piper nigrum L. Antiseptic
Piper nigrum L. Aperitif
Piper nigrum L. Carminative
Piper nigrum L. Catarrh
Piper nigrum L. Catecholaminic
Piper nigrum L. Chill
Piper nigrum L. Chokera
Piper nigrum L. Cold
Piper nigrum L. Colic
Piper nigrum L. Coma
Piper nigrum L. Condyloma
Piper nigrum L. Congestion
Piper nigrum L. Constipation
Piper nigrum L. Convulsion
Piper nigrum L. Corn
Piper nigrum L. Cough
Piper nigrum L. Cramp
Piper nigrum L. DebilityDermatosis
Piper nigrum L. Diaphoretic
Piper nigrum L. Diarrhea
Piper nigrum L. Digestive
Piper nigrum L. Diuretic
Piper nigrum L. Dog Bite
Piper nigrum L. Dry Mouth
Piper nigrum L. Dysentery
Piper nigrum L. Dysmenorrhea
Piper nigrum L. Dyspepsia
Piper nigrum L. Dysuria
Piper nigrum L. Emmenagogue
Piper nigrum L. Epididymosis
Piper nigrum L. Epilepsy
Piper nigrum L. Epinephrinogenic
Piper nigrum L. Escherichia
Piper nigrum L. Expectorant
Piper nigrum L. Favus
Piper nigrum L. Fever
Piper nigrum L. Frostbite
Piper nigrum L. Fungicide
Piper nigrum L. Fungus
Piper nigrum L. Furunculosis
Piper nigrum L. Galactorrhea
Piper nigrum L. Gas
Piper nigrum L. Gastrogogue
Piper nigrum L. Gastrosis
Piper nigrum L. Gingivosis
Piper nigrum L. Gonorrhea
Piper nigrum L. Gravel
Piper nigrum L. Hay Fever
Piper nigrum L. Head Cold
Piper nigrum L. Headache
Piper nigrum L. Hemorrhoid
Piper nigrum L. Hepatosis
Piper nigrum L. Hepatotonic
Piper nigrum L. Hiccup
Piper nigrum L. High Blood Pressure
Piper nigrum L. High Cholesterol
Piper nigrum L. HMG-CoA-Reductase Inhibitor
Piper nigrum L. Hypertensive
Piper nigrum L. Hypocholesterolemic
Piper nigrum L. Hypotensive
Piper nigrum L. Induration
Piper nigrum L. Infection
Piper nigrum L. Inflammation
Piper nigrum L. Insecticide
Piper nigrum L. Itch
Piper nigrum L. Larvicide
Piper nigrum L. Leishmaniasis
Piper nigrum L. Lethargy
Piper nigrum L. Malaria
Piper nigrum L. Mucososis
Piper nigrum L. Mutagenic
Piper nigrum L. Mycosis
Piper nigrum L. Nausea
Piper nigrum L. Nervousness
Piper nigrum L. Neuralgia
Piper nigrum L. Onychiosis
Piper nigrum L. Ophthalmia
Piper nigrum L. Pain
Piper nigrum L. Paralysis
Piper nigrum L. Paraplegia
Piper nigrum L. Parturition
Piper nigrum L. Peristaltic
Piper nigrum L. Phymata
Piper nigrum L. Positive Chronotropic
Piper nigrum L. Prolapse
Piper nigrum L. Respiradepressant
Piper nigrum L. Respirosis
Piper nigrum L. Rhinosis
Piper nigrum L. Ringworm
Piper nigrum L. Rubefacient
Piper nigrum L. Scabicide
Piper nigrum L. Scabies
Piper nigrum L. Scarlatina
Piper nigrum L. Scirrhus
Piper nigrum L. Secretagogue
Piper nigrum L. Sialagogue
Piper nigrum L. Sinusosis
Piper nigrum L. Snakebite
Piper nigrum L. Sore Throat
Piper nigrum L. Splenosis
Piper nigrum L. Staphylococcus
Piper nigrum L. Stimulant
Piper nigrum L. Stomachache
Piper nigrum L. Stomachic
Piper nigrum L. Swelling
Piper nigrum L. Taenicide
Piper nigrum L. Tinea
Piper nigrum L. Tonic
Piper nigrum L. Toothache
Piper nigrum L. Tumor
Piper nigrum L. Ulcer
Piper nigrum L. Urethrosis
Piper nigrum L. Urolithiasis
Piper nigrum L. Vertigo
Piper nigrum L. vomiting
Piper nigrum L. Wart
Piper nigrum L. Water Retention
Piper nigrum L. Wen
Piper nigrum L. Yeast

Metabolite list (11)

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
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00023774 External link 512 Fucostanol
/ Stigmasterol
/ Dihydro-beta-sitosterol
/ (24S)24-Ethylcholestain-3beta-ol
CHEMBL66943
CHEMBL186373
CHEMBL400247
CHEMBL1568947
D013265
5 / 0 / 0 1 / 0 No. 53 No. 11
C00032163 External link 512 Sitostanol
/ Stigmastanol
/ beta-Sitostanol
CHEMBL305498
CHEMBL252364
C021255
No. 68 No. 11
C00032087 External link 512 Octadecanoic acid
CHEMBL46403
C031183
15 / 17 / 19 6 / 1 No. 184 No. 68
C00019308 External link 512 Doursterol
/ Daucosterin
/ 3-O-beta-D-Glucopyranosyl sitosterol
/ beta-Sitosterol 3-O-beta-D-glucopyranoside
CHEMBL197711
CHEMBL506678
CHEMBL2304043
C011015
5 / 4 / 2 0 / 3 No. 520
C00031036 External link 512 Pipyahyine
No. 638
C00028813 External link 512 Pellitorine
C008778
No. 1863
C00031306 External link 512 Sarmentine
CHEMBL2205104
No. 3056
C00031479 External link 512 [(2E,4E)-Dodecadienoyl]-pyrrolidine
No. 3056
C00031853 External link 512 Hexadecanoylpyrrolidine
/ 1-Hexadecanoylpyrrolidine
CHEMBL1223443
No. 4618
C00031035 External link 512 Pipnoohine
No. 4837

Human Protein / Gene in interactions

34 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P06746 DNA polymerase beta Enzyme C00003672 C00019308 C00023774 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 C00019308 0 / 0
P00734 Prothrombin S1A C00003672 C00019308 4 / 2
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00003672 C00032087 1 / 1
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00003672 C00019308 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00003672 C00019308 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00003672 C00032087 3 / 2
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00032087 2 / 2
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00023774 0 / 0
P08183 Multidrug resistance protein 1 drug C00003672 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003672 0 / 1
P11473 Vitamin D3 receptor NR1I1 C00032087 2 / 3
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00032087 0 / 0
P15090 Fatty acid-binding protein, adipocyte Other cytosolic protein C00032087 0 / 0
Q9UGP5 DNA polymerase lambda Enzyme C00032087 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 2 / 0
P04150 Glucocorticoid receptor NR3C1 C00032087 0 / 1
P10828 Thyroid hormone receptor beta NR1A2 C00032087 3 / 1
P14679 Tyrosinase Oxidoreductase C00003672 4 / 2
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00003672 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00032087 3 / 3
P03372 Estrogen receptor NR3A1 C00003672 1 / 1
P09884 DNA polymerase alpha catalytic subunit Transferase C00023774 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00032087 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00032087 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003672 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00003672 0 / 1
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00032087 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00003672 1 / 0
O00255 Menin Unclassified protein C00032087 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00032087 1 / 2
P11388 DNA topoisomerase 2-alpha Isomerase C00023774 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00023774 0 / 0

7 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
9619 ABCG1, ABC8, WHITE1 ATP-binding cassette, sub-family G (WHITE), member 1 C00032087
6348 CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3 chemokine (C-C motif) ligand 3 C00032087
1906 EDN1, ET1, HDLCQ7, PPET1 endothelin 1 C00032087
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00032087
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00032087
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00032087
10599 SLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 solute carrier organic anion transporter family, member 1B1 C00023774

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (32)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#103470 Albinism, ocular, with sensorineural deafness P14679
#203100 Albinism, oculocutaneous, type ia; oca1a P14679
#606952 Albinism, oculocutaneous, type ib; oca1b P14679
#218030 Apparent mineralocorticoid excess; ame P80365
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#615363 Estrogen resistance; estrr P03372
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734
#188570 Thyroid hormone resistance, generalized, autosomal dominant; grth P10828
#274300 Thyroid hormone resistance, generalized, autosomal recessive; grth P10828
#145650 Thyroid hormone resistance, selective pituitary; prth P10828
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (28)

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)
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00026 Endometrial Cancer P03372 (marker)
H00599 46,XX disorders of sex development (Disorders related to androgen excess) P04150 (related)
P11511 (related)
H00036 Osteosarcoma P08684 (marker)
H00249 Thyroid hormone resistance syndrome P10828 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00794 Aromatase excess syndrome P11511 (related)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00038 Malignant melanoma P14679 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (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)
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)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

3 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003072 Cognition Disorders C00019308
C00032087
D002493 Central Nervous System Diseases C00019308
D013118 Spinal Cord Diseases C00019308