Species

KNApSAcK Entry

Organism name Piper philippinum
Genus Piper
Family Piperaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Piper
Linked NCBI taxonomy ID 13215
Linked level genus

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 (25)

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
C00004573 External link 512 3,7,4'-Tri-O-methylkaempferol
/ Kaempferol 3,7,4'-trimethyl ether
/ 5-Hydroxy-3,7,4'-trimethoxyflavone
/ 5-Hydroxy-3,7-dimethoxy-2-(4-methoxyphenyl)-4H-1-benzopyran-4-one
CHEMBL77686
No. 35 No. 15
C00003674 External link 512 Stigmasterol
/ beta-Stigmasterol
CHEMBL66943
CHEMBL186373
CHEMBL400247
CHEMBL1568947
D013265
5 / 0 / 0 1 / 0 No. 53 No. 11
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00034357 External link 512 (22E,24S)-Stigmast-4,22-dien-3-one
CHEMBL307549
No. 53 No. 11
C00027470 External link 512 Piperolactam A
CHEMBL387864
C457227
No. 125
C00034356 External link 512 Kusunokinin
/ (-)-Kusunokinin
No. 223 No. 21
C00034632 External link 512 Piperphilippinin I
No. 223 No. 21
C00034633 External link 512 Piperphilippinin II
/ (-)-Piperphilippinin II
No. 223 No. 21
C00034355 External link 512 Haplomyrfolin
/ (-)-Haplomyrfolin
No. 223 No. 21
C00000606 External link 512 (-)-Matairesinol
CHEMBL425148
C068935
1 / 0 / 0 No. 223 No. 21
C00034637 External link 512 Piperphilippinin VI
No. 282 No. 21
C00012483 External link 512 Betula pubescens
/ Caryophyllene oxide
/ trans-Caryophyllene oxide
/ beta-Caryophyllene epoxide
/ (-)-Epoxydihydrocaryophyllene
/ 6,7-Epoxy-3(15)-caryophyllene
/ (-)-beta-Caryophyllene epoxide
/ 4beta,5alpha-Epoxycaryophyllene
/ Caryophyllene 4beta,5alpha-epoxide
CHEMBL399036
CHEMBL508894
CHEMBL479134
CHEMBL1513806
CHEMBL1553274
3 / 1 / 3 No. 500
C00002608 External link 512 Hinokinin
/ Hinoquinin
/ (-)-Hinokinin
/ (-)-Hinoquinin
CHEMBL180970
CHEMBL182073
CHEMBL242011
C475934
2 / 1 / 1 No. 629 No. 21
C00023758 External link 512 Ergosta-4,6,8(14),22-tetraen-3-one
CHEMBL1801892
CHEMBL2040598
C015860
No. 768
C00002636 External link 512 Anisaldehyde
/ p-Anisaldehyde
CHEMBL161598
C024896
11 / 18 / 13 1 / 0 No. 1003
C00034635 External link 512 Piperphilippinin IV
/ (-)-Piperphilippinin IV
No. 1029 No. 21
C00034386 External link 512 3,4-Methylenedioxycinnamic acid
No. 2200
C00034395 External link 512 (E)-Methyl 4-methoxycinnamate
/ 4-Methoxy-trans-cinnamic acid
No. 2416
C00002757 External link 512 4-Methoxycinnamaldehyde
/ p-Methoxycinnamaldehyde
CHEMBL452173
No. 2748 No. 6
C00029536 External link 512 p-Anisic acid
/ 4-Methoxybenzoic acid
CHEMBL21932
C004520
3 / 2 / 3 No. 2930
C00034636 External link 512 Piperphilippinin V
No. 3222
C00034385 External link 512 3,4-Methylenedioxycinnamaldehyde
No. 3773
C00002666 External link 512 Piperonal
CHEMBL271663
C005454
3 / 4 / 4 No. 4093
C00031034 External link 512 Piperonylic acid
/ 3,4-Methylenedioxybenzoic acid
CHEMBL573781
C005455
2 / 0 / 0 No. 4093
C00034634 External link 512 Piperphilippinin III
/ (-)-Piperphilippinin III
No. 4573

Human Protein / Gene in interactions

35 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00002608 C00003672 C00012483 0 / 1
P00352 Retinal dehydrogenase 1 Enzyme C00002636 C00002666 C00031034 0 / 0
P03372 Estrogen receptor NR3A1 C00002636 C00003672 1 / 1
P06746 DNA polymerase beta Enzyme C00003672 C00003674 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00003672 C00012483 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00002608 C00003672 1 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00002636 C00003672 0 / 0
P14679 Tyrosinase Oxidoreductase C00002636 C00003672 4 / 2
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00002666 C00003672 1 / 1
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00003672 C00012483 0 / 1
P83916 Chromobox protein homolog 1 Unclassified protein C00002636 0 / 0
P34969 5-hydroxytryptamine receptor 7 Serotonin receptor C00003674 0 / 0
P00918 Carbonic anhydrase 2 Lyase C00029536 1 / 2
P04278 Sex hormone-binding globulin Secreted protein C00000606 0 / 0
P11509 Cytochrome P450 2A6 Cytochrome P450 2A6 C00002636 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00029536 0 / 0
P49841 Glycogen synthase kinase-3 beta Gsk C00003672 0 / 0
P08183 Multidrug resistance protein 1 drug C00003672 1 / 0
P00734 Prothrombin S1A C00003672 4 / 2
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00002636 1 / 1
P37231 Peroxisome proliferator-activated receptor gamma NR1C3 C00002636 5 / 3
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00002636 1 / 1
P28482 Mitogen-activated protein kinase 1 Erk C00031034 0 / 0
P10828 Thyroid hormone receptor beta NR1A2 C00002636 3 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00002666 3 / 3
P16473 Thyrotropin receptor Glycohormone receptor C00003672 3 / 2
P09884 DNA polymerase alpha catalytic subunit Transferase C00003674 0 / 0
P51580 Thiopurine S-methyltransferase Enzyme C00029536 1 / 1
P08047 Transcription factor Sp1 Unclassified protein C00003672 0 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 2 / 0
P10275 Androgen receptor NR3C4 C00002636 3 / 4
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003672 1 / 1
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00003672 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00003674 0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase C00003674 0 / 0

2 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
8989 TRPA1, ANKTM1, FEPS transient receptor potential cation channel, subfamily A, member 1 C00002636
10599 SLCO1B1, HBLRR, LST-1, LST1, OATP-C, OATP1B1, OATP2, OATPC, SLC21A6 solute carrier organic anion transporter family, member 1B1 C00003674

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (37)

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
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#218030 Apparent mineralocorticoid excess; ame P80365
%606641 Body mass index; bmi P37231
#609338 Carotid intimal medial thickness 1 P37231
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#615363 Estrogen resistance; estrr P03372
#613163 Gaba-transaminase deficiency P80404
#137800 Glioma susceptibility 1; glm1 P37231
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#604367 Lipodystrophy, familial partial, type 3; fpld3 P37231
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#601665 Obesity P37231
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#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
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#607250 Spinocerebellar ataxia, autosomal recessive, with axonal neuropathy; scan1 Q9NUW8
#601367 Stroke, ischemic P00734
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#610460 Thiopurine s-methyltransferase deficiency P51580
#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

KEGG DISEASE (28)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
H00026 Endometrial Cancer P03372 (marker)
H00036 Osteosarcoma P08684 (marker)
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)
H00249 Thyroid hormone resistance syndrome P10828 (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)
H00032 Thyroid cancer P37231 (related)
H00409 Type II diabetes mellitus P37231 (related)
H00420 Familial partial lipodystrophy (FPL) P37231 (related)
H00964 Thiopurine S-methyltransferase deficiency (TPMT deficiency) P51580 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H01257 GABA-transaminase deficiency P80404 (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)