Organism name | Piper philippinum |
---|---|
Genus | Piper |
Family | Piperaceae |
Kingdom | Plantae |
Linked NCBI taxonomy name | Piper |
---|---|
Linked NCBI taxonomy ID | 13215 |
Linked level | genus |
Family in NCBI taxonomy | Piperaceae |
---|---|
ID | 16739 |
Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
---|---|
ID | 33090 |
Plant class | Magnoliophyta |
---|---|
ID | 3398 |
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
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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
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Stigmasterol
/ beta-Stigmasterol |
CHEMBL66943
CHEMBL186373 CHEMBL400247 CHEMBL1568947 |
D013265
|
5 / 0 / 0 | 1 / 0 | No. 53 | No. 11 |
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C00003672
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Sitosterol
/ beta-sitosterl / (-)-beta-Sitosterol / Stigmast-5-en-3beta-ol |
CHEMBL221542
CHEMBL1398443 CHEMBL1875388 |
17 / 19 / 12 | No. 53 | No. 11 |
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||
C00034357
![]() |
(22E,24S)-Stigmast-4,22-dien-3-one
|
CHEMBL307549
|
No. 53 | No. 11 |
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|||
C00027470
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Piperolactam A
|
CHEMBL387864
|
C457227
|
No. 125 |
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|||
C00034356
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Kusunokinin
/ (-)-Kusunokinin |
No. 223 | No. 21 |
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||||
C00034632
![]() |
Piperphilippinin I
|
No. 223 | No. 21 |
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||||
C00034633
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Piperphilippinin II
/ (-)-Piperphilippinin II |
No. 223 | No. 21 |
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||||
C00034355
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Haplomyrfolin
/ (-)-Haplomyrfolin |
No. 223 | No. 21 |
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||||
C00000606
![]() |
(-)-Matairesinol
|
CHEMBL425148
|
C068935
|
1 / 0 / 0 | No. 223 | No. 21 |
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|
C00034637
![]() |
Piperphilippinin VI
|
No. 282 | No. 21 |
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||||
C00012483
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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 |
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|||
C00002608
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Hinokinin
/ Hinoquinin / (-)-Hinokinin / (-)-Hinoquinin |
CHEMBL180970
CHEMBL182073 CHEMBL242011 |
C475934
|
2 / 1 / 1 | No. 629 | No. 21 |
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|
C00023758
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Ergosta-4,6,8(14),22-tetraen-3-one
|
CHEMBL1801892
CHEMBL2040598 |
C015860
|
No. 768 |
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|||
C00002636
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Anisaldehyde
/ p-Anisaldehyde |
CHEMBL161598
|
C024896
|
11 / 18 / 13 | 1 / 0 | No. 1003 |
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|
C00034635
![]() |
Piperphilippinin IV
/ (-)-Piperphilippinin IV |
No. 1029 | No. 21 |
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||||
C00034386
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3,4-Methylenedioxycinnamic acid
|
No. 2200 |
![]() |
|||||
C00034395
![]() |
(E)-Methyl 4-methoxycinnamate
/ 4-Methoxy-trans-cinnamic acid |
No. 2416 |
![]() |
|||||
C00002757
![]() |
4-Methoxycinnamaldehyde
/ p-Methoxycinnamaldehyde |
CHEMBL452173
|
No. 2748 | No. 6 |
![]() |
|||
C00029536
![]() |
p-Anisic acid
/ 4-Methoxybenzoic acid |
CHEMBL21932
|
C004520
|
3 / 2 / 3 | No. 2930 |
![]() |
||
C00034636
![]() |
Piperphilippinin V
|
No. 3222 |
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|||||
C00034385
![]() |
3,4-Methylenedioxycinnamaldehyde
|
No. 3773 |
![]() |
|||||
C00002666
![]() |
Piperonal
|
CHEMBL271663
|
C005454
|
3 / 4 / 4 | No. 4093 |
![]() |
||
C00031034
![]() |
Piperonylic acid
/ 3,4-Methylenedioxybenzoic acid |
CHEMBL573781
|
C005455
|
2 / 0 / 0 | No. 4093 |
![]() |
||
C00034634
![]() |
Piperphilippinin III
/ (-)-Piperphilippinin III |
No. 4573 |
![]() |
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 |
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
|
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 | 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)
|