Species

KNApSAcK Entry

Organism name Alangium lamarckii
Genus Alangium
Family Cornaceae / Aucubaceae / Garryaceae / Helwingiaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Alangium
Linked NCBI taxonomy ID 16896
Linked level genus

Family

Family in NCBI taxonomy Cornaceae
ID 42219

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Metabolite list (33)

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
C00010604 External link 512 Loganic acid
CHEMBL1081585
CHEMBL1079678
CHEMBL1356464
CHEMBL1452775
C002947
6 / 8 / 7 No. 64 No. 36
C00037307 External link 512 Iridoid glycoside
/ (-)-Iridoid glycoside
No. 64 No. 36
C00037800 External link 512 Secologanoside
No. 100 No. 36
C00032760 External link 512 (-)-Benzyl beta-primeveroside
/ Benzyl alcohol beta-D-xylopyranosyl (1->6)-beta-D-glucopyranoside
CHEMBL1371061
C069904
3 / 1 / 1 No. 128 No. 72
C00036637 External link 512 6'-O-alpha-D-glucopyranosylloganic acid
No. 222
C00001835 External link 512 Cephaeline
CHEMBL255708
CHEMBL486005
CHEMBL1616444
C005963
3 / 0 / 0 6 / 0 No. 510 No. 4
C00027421 External link 512 Neocephaeline
/ (-)-Neocephaeline
No. 510 No. 4
C00001796 External link 512 Alangimarckine
No. 510 No. 4
C00001907 External link 512 Psychotrine
CHEMBL463445
No. 510 No. 4
C00001795 External link 512 Alangicine
No. 510 No. 4
C00027397 External link 512 Isotubulosine
CHEMBL518568
CHEMBL535307
CHEMBL1254284
CHEMBL1369261
19 / 18 / 10 No. 510 No. 4
C00026848 External link 512 Deoxytubulosine
/ 8'-Deoxytubulosine
No. 510 No. 4
C00027245 External link 512 10-O-Demethylcephaeline
/ (-)-10-Demethylcephaeline
No. 510 No. 4
C00027384 External link 512 Isocephaeline
CHEMBL255708
CHEMBL486005
CHEMBL1616444
3 / 0 / 0 No. 510 No. 4
C00001778 External link 512 Tubulosine
/ (-)-Tubulosine
CHEMBL518568
CHEMBL535307
CHEMBL1254284
CHEMBL1369261
C009805
19 / 18 / 10 No. 510 No. 4
C00027550 External link 512 Isoalangiside
CHEMBL486383
CHEMBL2138751
2 / 0 / 0 No. 577 No. 4
C00027567 External link 512 Neoalangiside
No. 577 No. 4
C00001798 External link 512 Alangiside
CHEMBL486383
CHEMBL2138751
2 / 0 / 0 No. 577 No. 4
C00027578 External link 512 O-Methylisoalangiside
No. 577 No. 4
C00010794 External link 512 Sweroside
CHEMBL456137
C049412
1 / 0 / 0 No. 806 No. 36
C00027252 External link 512 3'-O-beta-D-glucopyranosylalangiside
/ (-)-3'-O-beta-D-glucopyranosylalangiside
No. 1411
C00027254 External link 512 6'-alpha-D-glucopyranosylalangiside
/ (-)-6'-alpha-D-glucopyranosylalangiside
No. 1411
C00027255 External link 512 6'-O-alpha-D-Xylopyranosylalangiside
/ (-)-6'-O-alpha-D-Xylopyranosylalangiside
No. 1411
C00027256 External link 512 6'-O-beta-D-glucopyranosylalangiside
/ (-)-6'-O-beta-D-glucopyranosylalangiside
No. 1411
C00001805 External link 512 Ankorine
No. 2276 No. 4
C00027270 External link 512 Alangine
/ (-)-Alangine
No. 2276 No. 4
C00027473 External link 512 Protoemetinol
No. 2276 No. 4
C00027472 External link 512 Protoemetine
No. 2276 No. 4
C00027481 External link 512 Salsoline
/ (-)-O7-Methylsalsolinol
CHEMBL1187592
CHEMBL1192723
CHEMBL1532461
C032837
3 / 4 / 3 No. 2962 No. 4
C00001794 External link 512 Alamarine
No. 2972
C00001797 External link 512 Alangimarine
No. 2972
C00027509 External link 512 2'-O-trans-Sinapoylalangiside
No. 5314
C00027508 External link 512 2'-O-trans-Feruloylalangiside
/ (-)-2'-O-trans-Feruloylalangiside
No. 5314

Human Protein / Gene in interactions

29 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
O75496 Geminin Unclassified protein C00001778 C00001798 C00027397 C00027550 C00032760 0 / 0
Q16665 Hypoxia-inducible factor 1-alpha Transcription Factor C00001778 C00001835 C00027384 C00027397 0 / 0
O94925 Glutaminase kidney isoform, mitochondrial Enzyme C00001778 C00001798 C00027397 C00027550 0 / 0
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00001778 C00027397 C00027481 1 / 0
O75874 Isocitrate dehydrogenase [NADP] cytoplasmic Enzyme C00001778 C00010604 C00027397 1 / 0
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein C00001778 C00010604 C00027397 0 / 0
P84022 Mothers against decapentaplegic homolog 3 Unclassified protein C00001778 C00010604 C00027397 2 / 0
P18433 Receptor-type tyrosine-protein phosphatase alpha Receptor tyrosine-protein phosphatase C00001778 C00027397 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00001778 C00027397 4 / 1
P20701 Integrin alpha-L Membrane receptor C00001835 C00027384 0 / 0
Q9H0H5 Rac GTPase-activating protein 1 Unclassified protein C00001778 C00027397 0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein C00001778 C00027397 7 / 3
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00001778 C00027397 0 / 1
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00001778 C00027397 0 / 0
Q99700 Ataxin-2 Unclassified protein C00001778 C00027397 1 / 1
P27540 Aryl hydrocarbon receptor nuclear translocator Unclassified protein C00001835 C00027384 0 / 0
P23467 Receptor-type tyrosine-protein phosphatase beta Receptor tyrosine-protein phosphatase C00001778 C00027397 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00001778 C00027397 1 / 1
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00001778 C00027397 0 / 1
O75164 Lysine-specific demethylase 4A Enzyme C00001778 C00027397 0 / 0
Q06710 Paired box protein Pax-8 Unclassified protein C00001778 C00027397 1 / 2
P10636 Microtubule-associated protein tau Unclassified protein C00010604 4 / 3
P07900 Heat shock protein HSP 90-alpha Other cytosolic protein C00010794 0 / 0
B2RXH2 Lysine-specific demethylase 4E Enzyme C00032760 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00027481 0 / 0
P60033 CD81 antigen Unclassified protein C00010604 1 / 1
P01215 Glycoprotein hormones alpha chain Unclassified protein C00010604 0 / 3
P10253 Lysosomal alpha-glucosidase Hydrolase C00032760 1 / 1
Q99714 3-hydroxyacyl-CoA dehydrogenase type-2 Enzyme C00027481 3 / 3

6 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
6347 CCL2, GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1, SCYA2, SMC-CF chemokine (C-C motif) ligand 2 C00001835
6351 CCL4, ACT2, AT744.1, G-26, HC21, LAG-1, LAG1, MIP-1-beta, MIP1B, MIP1B1, SCYA2, SCYA4 chemokine (C-C motif) ligand 4 C00001835
6352 CCL5, D17S136E, RANTES, SCYA5, SIS-delta, SISd, TCP228, eoCP chemokine (C-C motif) ligand 5 C00001835
3570 IL6R, CD126, IL-6R-1, IL-6RA, IL6Q, IL6RA, IL6RQ, gp80 interleukin 6 receptor C00001835
3576 IL8, CXCL8, GCP-1, GCP1, LECT, LUCT, LYNAP, MDNCF, MONAP, NAF, NAP-1, NAP1 interleukin 8 C00001835
7422 VEGFA, MVCD1, VEGF, VPF vascular endothelial growth factor A C00001835

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (27)

OMIM preferred title UniProt
#300438 17-beta-hydroxysteroid dehydrogenase x deficiency Q99714
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#114500 Colorectal cancer; crc P84022
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#600274 Frontotemporal dementia; ftd P10636
#137800 Glioma susceptibility 1; glm1 O75874
#232300 Glycogen storage disease ii P10253
#218700 Hypothyroidism, congenital, nongoitrous, 2; chng2 Q06710
#613496 Immunodeficiency, common variable, 6; cvid6 P60033
#613795 Loeys-dietz syndrome, type 3; lds3 P84022
#174800 Mccune-albright syndrome; mas P63092
#300705 Mental retardation, x-linked 17; mrx17 Q99714
#300220 Mental retardation, x-linked, syndromic 10; mrxs10 Q99714
#166350 Osseous heteroplasia, progressive; poh P63092
#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
#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
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (20)

KEGG name UniProt
H00081 Hashimoto's thyroiditis P01215 (marker)
H00082 Graves' disease P01215 (marker)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P01215 (marker)
Q06710 (related)
H00036 Osteosarcoma P08684 (marker)
H00069 Glycogen storage diseases (GSD) P10253 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H01205 Coumarin resistance P11712 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00088 Common variable immunodeficiency (CVID) P60033 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (related)
H00032 Thyroid cancer Q06710 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H00063 Spinocerebellar ataxia (SCA) Q99700 (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)