Species

KNApSAcK Entry

Organism name Dryopteris crassirhizoma
Genus Dryopteris
Family Dryopteridaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Dryopteris crassirhizoma
Linked NCBI taxonomy ID 97234
Linked level species

Family

Family in NCBI taxonomy Dryopteridaceae
ID 29607

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Euphyllophyta
ID 78536

Metabolite list (24)

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
C00013790 External link 512 Crassirhizomoside C
/ Kaempferol 3-(2'',3''-diacetylrhamnoside)-7-rhamnoside
/ 7-[(6-Deoxy-alpha-L-mannopyranosyl)oxy]-3-[(2,3-di-O-acetyl-6-deoxy-alpha-L-mannopyranosyl)oxy]-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one
No. 1 No. 15
C00005896 External link 512 Sutchuenoside A
/ Kaempferol 3-O-alpha-L-(4-O-acetyl)rhamnopyranoside-7-O-alpha-L-rhamnopyranoside
No. 1 No. 15
C00005189 External link 512 Kaempferitrin
/ Kaempferol 3,7-di-O-rhamnoside
/ Kaempferol 3,7-di-O-alpha-rhamnopyranoside
CHEMBL251766
C042728
2 / 5 / 5 No. 1 No. 15
C00030021 External link 512 Crassirhizomoside B
No. 1 No. 15
C00030020 External link 512 Crassirhizomoside A
No. 1 No. 15
C00005140 External link 512 Afzelin
/ Kaempferol 3-O-alpha-rhamnoside
/ Kaempferol 3-O-alpha-L-rhamnopyranoside
CHEMBL240528
CHEMBL515798
C477954
4 / 2 / 2 No. 2 No. 15
C00005150 External link 512 Kaempferol 7-rhamnoside
/ Kaempferol 7-O-rhamnoside
/ Kaempferol 7-O-alpha-L-rhamnopyranoside
CHEMBL1288270
CHEMBL1289337
No. 2 No. 15
C00003558 External link 512 Ursolic acid
CHEMBL297810
CHEMBL56048
CHEMBL300594
CHEMBL169
CHEMBL176234
CHEMBL491715
CHEMBL1316667
CHEMBL1555307
CHEMBL1593360
CHEMBL1979720
C005466
47 / 26 / 33 15 / 12 No. 13 No. 51
C00030156 External link 512 Dryopteric acid A
/ (+)-4-epi-Dryopteric B
No. 23 No. 51
C00030157 External link 512 Dryopteric acid B
No. 23 No. 51
C00008168 External link 512 Desmethoxymatteucinol
CHEMBL53439
5 / 1 / 4 No. 25 No. 14
C00008243 External link 512 Matteucinol
CHEMBL1224711
C049059
No. 25 No. 14
C00030750 External link 512 Methoxymatteucin
No. 25 No. 14
C00029416 External link 512 Picraquassioside D
/ (-)-Picraquassioside D
/ 1-beta-D-Glucopyranosyloxy-3-methoxy-5-hydroxybenzene
No. 45 No. 72
C00009317 External link 512 Dryopteric acid
/ 4beta-Carboxymethyl-(-)-epicatechin
No. 52 No. 14
C00003672 External link 512 Sitosterol
/ beta-sitosterl
/ (-)-beta-Sitosterol
/ Stigmast-5-en-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00001238 External link 512 Stearic acid
CHEMBL46403
C031183
15 / 17 / 19 6 / 1 No. 184 No. 68
C00003746 External link 512 Fernen
/ Fernene
/ Fern-9-ene
/ Fern 9(11)-ene
No. 198 No. 52
C00029295 External link 512 (+)-Catechin 6-C-beta-D-glucopyranoside
No. 261 No. 14
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
C00030518 External link 512 Isobiflorin
No. 1013 No. 15
C00002417 External link 512 Biflorin
CHEMBL463312
No. 1013 No. 15
C00030158 External link 512 Dryopteroside
/ (+)-Dryopteroside
No. 1962
C00000094 External link 512 2iP
/ N6-(delta2-Isopentenyl)adenine
CHEMBL476189
C001478
5 / 2 / 3 18 / 0 No. 2879

Human Protein / Gene in interactions

68 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00000094 C00003558 C00003672 C00005140 1 / 0
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00000094 C00003558 C00003672 C00005140 0 / 1
P49841 Glycogen synthase kinase-3 beta Gsk C00003558 C00003672 C00019308 0 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00000094 C00003558 C00003672 0 / 1
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00003558 C00003672 C00019308 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00000094 C00003558 C00003672 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00000094 C00003558 C00003672 1 / 1
P06746 DNA polymerase beta Enzyme C00003558 C00003672 C00019308 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00003558 C00003672 C00019308 0 / 0
P19838 Nuclear factor NF-kappa-B p105 subunit Transcription Factor C00001238 C00003558 0 / 0
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00003558 C00003672 1 / 1
P35354 Prostaglandin G/H synthase 2 Oxidoreductase C00003558 C00008168 0 / 3
P11511 Cytochrome P450 19A1 Cytochrome P450 19A1 C00001238 C00003558 2 / 2
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00001238 C00003672 1 / 1
P16473 Thyrotropin receptor Glycohormone receptor C00001238 C00003672 3 / 2
P10828 Thyroid hormone receptor beta NR1A2 C00001238 C00003558 3 / 1
P00734 Prothrombin S1A C00003672 C00019308 4 / 2
P83916 Chromobox protein homolog 1 Unclassified protein C00003558 C00008168 0 / 0
O00255 Menin Unclassified protein C00001238 C00003558 2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme C00001238 C00003558 1 / 2
P23219 Prostaglandin G/H synthase 1 Oxidoreductase C00003558 C00008168 0 / 0
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00003558 0 / 0
P28845 Corticosteroid 11-beta-dehydrogenase isozyme 1 Enzyme C00003558 1 / 1
Q9UQL6 Histone deacetylase 5 Hydrolase C00003558 0 / 0
Q92830 Histone acetyltransferase KAT2A Enzyme C00003558 0 / 0
P04035 3-hydroxy-3-methylglutaryl-coenzyme A reductase Oxidoreductase C00001238 0 / 0
P15121 Aldose reductase Enzyme C00003558 0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase C00005189 0 / 0
Q04206 Transcription factor p65 Transcription Factor C00003558 0 / 0
Q9UGP5 DNA polymerase lambda Enzyme C00001238 0 / 0
P10586 Receptor-type tyrosine-protein phosphatase F Receptor tyrosine-protein phosphatase C00003558 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00003558 0 / 0
P08183 Multidrug resistance protein 1 drug C00003672 1 / 0
P04150 Glucocorticoid receptor NR3C1 C00001238 0 / 1
P02545 Prelamin-A/C Unclassified protein C00003558 11 / 10
P14679 Tyrosinase Oxidoreductase C00003672 4 / 2
P16083 Ribosyldihydronicotinamide dehydrogenase [quinone] Enzyme C00005140 0 / 0
Q96RI1 Bile acid receptor NR1H4 C00003558 0 / 0
O15379 Histone deacetylase 3 Hydrolase C00003558 0 / 0
P18433 Receptor-type tyrosine-protein phosphatase alpha Receptor tyrosine-protein phosphatase C00003558 0 / 0
O75604 Ubiquitin carboxyl-terminal hydrolase 2 Enzyme C00003558 0 / 0
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00001238 3 / 3
P03372 Estrogen receptor NR3A1 C00003672 1 / 1
P56524 Histone deacetylase 4 Hydrolase C00003558 1 / 1
Q8TDU6 G-protein coupled bile acid receptor 1 Steroid-like ligand receptor C00003558 0 / 0
P30305 M-phase inducer phosphatase 2 Ser_Thr_Tyr C00003558 0 / 0
P16050 Arachidonate 15-lipoxygenase Enzyme C00001238 0 / 0
P24666 Low molecular weight phosphotyrosine protein phosphatase Tyr C00003558 0 / 0
Q13547 Histone deacetylase 1 Hydrolase C00003558 0 / 0
P98170 E3 ubiquitin-protein ligase XIAP Other cytosolic protein C00005140 1 / 1
Q9UNA4 DNA polymerase iota Enzyme C00008168 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00001238 2 / 3
Q07869 Peroxisome proliferator-activated receptor alpha NR1C1 C00003558 0 / 0
P17706 Tyrosine-protein phosphatase non-receptor type 2 Tyr C00003558 0 / 1
Q9UBN7 Histone deacetylase 6 Hydrolase C00003558 0 / 0
P29350 Tyrosine-protein phosphatase non-receptor type 6 Tyr C00003558 0 / 0
O14746 Telomerase reverse transcriptase Enzyme C00005189 5 / 5
P15090 Fatty acid-binding protein, adipocyte Other cytosolic protein C00001238 0 / 0
P23469 Receptor-type tyrosine-protein phosphatase epsilon Receptor tyrosine-protein phosphatase C00003558 0 / 0
Q9UBT6 DNA polymerase kappa Enzyme C00001238 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00003558 0 / 0
O60218 Aldo-keto reductase family 1 member B10 Enzyme C00003558 0 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00003558 1 / 0
P49798 Regulator of G-protein signaling 4 Unclassified protein C00003672 2 / 0
Q99700 Ataxin-2 Unclassified protein C00008168 1 / 1
Q13951 Core-binding factor subunit beta Unclassified protein C00003558 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00003558 1 / 4
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00003558 0 / 0

39 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
440 ASNS, TS11 asparagine synthetase (glutamine-hydrolyzing) (EC:6.3.5.4) C00000094
694 BTG1 B-cell translocation gene 1, anti-proliferative C00000094
10681 GNB5, GB5 guanine nucleotide binding protein (G protein), beta 5 C00000094
182 JAG1, AGS, AHD, AWS, CD339, HJ1, JAGL1 jagged 1 C00000094
9818 NUPL1, PRO2463 nucleoporin like 1 C00000094
5142 PDE4B, DPDE4, PDE4B5, PDEIVB phosphodiesterase 4B, cAMP-specific (EC:3.1.4.17) C00000094
8544 PIR pirin (iron-binding nuclear protein) (EC:1.13.11.24) C00000094
5366 PMAIP1, APR, NOXA phorbol-12-myristate-13-acetate-induced protein 1 C00000094
9360 PPIG, CARS-Cyp, CYP, SCAF10, SRCyp peptidylprolyl isomerase G (cyclophilin G) (EC:5.2.1.8) C00000094
5782 PTPN12, PTP-PEST, PTPG1 protein tyrosine phosphatase, non-receptor type 12 (EC:3.1.3.48) C00000094
5774 PTPN3, PTP-H1, PTPH1 protein tyrosine phosphatase, non-receptor type 3 (EC:3.1.3.48) C00000094
6004 RGS16, A28-RGS14, A28-RGS14P, RGS-R regulator of G-protein signaling 16 C00000094
6016 RIT1, NS8, RIBB, RIT, ROC1 Ras-like without CAAX 1 C00000094
6286 S100P, MIG9 S100 calcium binding protein P C00000094
7029 TFDP2, DP2 transcription factor Dp-2 (E2F dimerization partner 2) C00000094
7127 TNFAIP2, B94, EXOC3L3 tumor necrosis factor, alpha-induced protein 2 C00000094
7296 TXNRD1, GRIM-12, TR, TR1, TRXR1, TXNR thioredoxin reductase 1 (EC:1.8.1.9) C00000094
7431 VIM, CTRCT30 vimentin C00000094
9131 AIFM1, AIF, CMTX4, COWCK, COXPD6, PDCD8 apoptosis-inducing factor, mitochondrion-associated, 1 C00003558
578 BAK1, BAK, BAK-LIKE, BCL2L7, CDN1 BCL2-antagonist/killer 1 C00003558
581 BAX, BCL2L4 BCL2-associated X protein C00003558
596 BCL2, Bcl-2, PPP1R50 B-cell CLL/lymphoma 2 C00003558
836 CASP3, CPP32, CPP32B, SCA-1 caspase 3, apoptosis-related cysteine peptidase (EC:3.4.22.56) C00003558
841 CASP8, ALPS2B, CAP4, Casp-8, FLICE, MACH, MCH5 caspase 8, apoptosis-related cysteine peptidase (EC:3.4.22.61) C00003558
54205 CYCS, CYC, HCS, THC4 cytochrome c, somatic C00003558
1557 CYP2C19, CPCJ, CYP2C, P450C2C, P450IIC19 cytochrome P450, family 2, subfamily C, polypeptide 19 (EC:1.14.13.48 1.14.13.49 1.14.13.80) C00003558
3383 ICAM1, BB2, CD54, P3.58 intercellular adhesion molecule 1 C00003558
4313 MMP2, CLG4, CLG4A, MMP-II, MONA, TBE-1 matrix metallopeptidase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) (EC:3.4.24.24) C00003558
4318 MMP9, CLG4B, GELB, MANDP2, MMP-9 matrix metallopeptidase 9 (gelatinase B, 92kDa gelatinase, 92kDa type IV collagenase) (EC:3.4.24.35) C00003558
142 PARP1, ADPRT, ADPRT_1, ADPRT1, ARTD1, PARP, PARP-1, PPOL, pADPRT-1 poly (ADP-ribose) polymerase 1 (EC:2.4.2.30) C00003558
7040 TGFB1, CED, DPD1, LAP, TGFB, TGFbeta transforming growth factor, beta 1 C00003558
7150 TOP1, TOPI topoisomerase (DNA) I (EC:5.99.1.2) C00003558
7153 TOP2A, TOP2, TP2A topoisomerase (DNA) II alpha 170kDa (EC:5.99.1.3) C00003558
9619 ABCG1, ABC8, WHITE1 ATP-binding cassette, sub-family G (WHITE), member 1 C00001238
6348 CCL3, G0S19-1, LD78ALPHA, MIP-1-alpha, MIP1A, SCYA3 chemokine (C-C motif) ligand 3 C00001238
1906 EDN1, ET1, HDLCQ7, PPET1 endothelin 1 C00001238
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00001238
5465 PPARA, NR1C1, PPAR, PPARalpha, hPPAR peroxisome proliferator-activated receptor alpha C00001238
10891 PPARGC1A, LEM6, PGC-1(alpha), PGC-1v, PGC1, PGC1A, PPARGC1 peroxisome proliferator-activated receptor gamma, coactivator 1 alpha C00001238

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (54)

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
#609135 Aplastic anemia O14746
#218030 Apparent mineralocorticoid excess; ame P80365
#613546 Aromatase deficiency P11511
#139300 Aromatase excess syndrome; aexs P11511
#600430 Brachydactyly-mental retardation syndrome; bdmr P56524
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#604931 Cortisone reductase deficiency 1; cortrd1 P28845
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#613989 Dyskeratosis congenita, autosomal dominant, 2; dkca2 O14746
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#615363 Estrogen resistance; estrr P03372
#137800 Glioma susceptibility 1; glm1 O75874
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#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
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#300635 Lymphoproliferative syndrome, x-linked, 2; xlp2 P98170
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#615134 Melanoma, cutaneous malignant, susceptibility to, 9; cmm9 O14746
#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
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#614390 Pregnancy loss, recurrent, susceptibility to, 2; rprgl2 P00734
#613679 Prothrombin deficiency, congenital P00734
#614742 Pulmonary fibrosis and/or bone marrow failure, telomere-related, 1; pfbmft1 O14746
#178500 Pulmonary fibrosis, idiopathic; ipf O14746
#275210 Restrictive dermopathy, lethal P02545
#604906 Schizophrenia 9; sczd9 P49798
#181500 Schizophrenia; sczd P49798
#601800 Skin/hair/eye pigmentation, variation in, 3; shep3 P14679
#183090 Spinocerebellar ataxia 2; sca2 Q99700
#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 (53)

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)
H00764 Cri du chat syndrome O14746 (related)
H01132 Aplastic anemia (AA) O14746 (related)
H01299 Idiopathic pulmonary fibrosis O14746 (related)
H00022 Bladder cancer O14746 (marker)
H00024 Prostate cancer O14746 (marker)
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (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)
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)
H00408 Type I diabetes mellitus P17706 (related)
H01111 Cortisone reductase deficiency (CRD) P28845 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00017 Esophageal cancer P35354 (related)
H00025 Penile cancer P35354 (related)
H00046 Cholangiocarcinoma P35354 (related)
H00561 Brachydacytly-mental retardation syndrome and Smith-Magenis syndrome P56524 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H00107 Other well-defined immunodeficiency syndromes P98170 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
Q03164 (related)
Q03164 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (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

15 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D003072 Cognition Disorders C00019308
C00001238
D007249 Inflammation C00003558
D002471 Cell Transformation, Neoplastic C00003558
D003921 Diabetes Mellitus, Experimental C00003558
D006943 Hyperglycemia C00003558
D006949 Hyperlipidemias C00003558
D006965 Hyperplasia C00003558
D006528 Carcinoma, Hepatocellular C00003558
D008103 Liver Cirrhosis C00003558
D017202 Myocardial Ischemia C00003558
D009369 Neoplasms C00003558
D012878 Skin Neoplasms C00003558
D002493 Central Nervous System Diseases C00019308
D001284 Atrophy C00003558
D013118 Spinal Cord Diseases C00019308