| Organism name | Alangium lamarckii |
|---|---|
| Genus | Alangium |
| Family | Cornaceae / Aucubaceae / Garryaceae / Helwingiaceae |
| Kingdom | Plantae |
| Linked NCBI taxonomy name | Alangium |
|---|---|
| Linked NCBI taxonomy ID | 16896 |
| Linked level | genus |
| Family in NCBI taxonomy | Cornaceae |
|---|---|
| ID | 42219 |
| Kingdom (Superkingdom) in NCBI taxonomy | Viridiplantae |
|---|---|
| ID | 33090 |
| Plant class | asterids |
|---|---|
| ID | 71274 |
| 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
|
Loganic acid
|
CHEMBL1081585
CHEMBL1079678 CHEMBL1356464 CHEMBL1452775 |
C002947
|
6 / 8 / 7 | No. 64 | No. 36 |
|
|
|
C00037307
|
Iridoid glycoside
/ (-)-Iridoid glycoside |
No. 64 | No. 36 |
|
||||
|
C00037800
|
Secologanoside
|
No. 100 | No. 36 |
|
||||
|
C00032760
|
(-)-Benzyl beta-primeveroside
/ Benzyl alcohol beta-D-xylopyranosyl (1->6)-beta-D-glucopyranoside |
CHEMBL1371061
|
C069904
|
3 / 1 / 1 | No. 128 | No. 72 |
|
|
|
C00036637
|
6'-O-alpha-D-glucopyranosylloganic acid
|
No. 222 |
|
|||||
|
C00001835
|
Cephaeline
|
CHEMBL255708
CHEMBL486005 CHEMBL1616444 |
C005963
|
3 / 0 / 0 | 6 / 0 | No. 510 | No. 4 |
|
|
C00027421
|
Neocephaeline
/ (-)-Neocephaeline |
No. 510 | No. 4 |
|
||||
|
C00001796
|
Alangimarckine
|
No. 510 | No. 4 |
|
||||
|
C00001907
|
Psychotrine
|
CHEMBL463445
|
No. 510 | No. 4 |
|
|||
|
C00001795
|
Alangicine
|
No. 510 | No. 4 |
|
||||
|
C00027397
|
Isotubulosine
|
CHEMBL518568
CHEMBL535307 CHEMBL1254284 CHEMBL1369261 |
19 / 18 / 10 | No. 510 | No. 4 |
|
||
|
C00026848
|
Deoxytubulosine
/ 8'-Deoxytubulosine |
No. 510 | No. 4 |
|
||||
|
C00027245
|
10-O-Demethylcephaeline
/ (-)-10-Demethylcephaeline |
No. 510 | No. 4 |
|
||||
|
C00027384
|
Isocephaeline
|
CHEMBL255708
CHEMBL486005 CHEMBL1616444 |
3 / 0 / 0 | No. 510 | No. 4 |
|
||
|
C00001778
|
Tubulosine
/ (-)-Tubulosine |
CHEMBL518568
CHEMBL535307 CHEMBL1254284 CHEMBL1369261 |
C009805
|
19 / 18 / 10 | No. 510 | No. 4 |
|
|
|
C00027550
|
Isoalangiside
|
CHEMBL486383
CHEMBL2138751 |
2 / 0 / 0 | No. 577 | No. 4 |
|
||
|
C00027567
|
Neoalangiside
|
No. 577 | No. 4 |
|
||||
|
C00001798
|
Alangiside
|
CHEMBL486383
CHEMBL2138751 |
2 / 0 / 0 | No. 577 | No. 4 |
|
||
|
C00027578
|
O-Methylisoalangiside
|
No. 577 | No. 4 |
|
||||
|
C00010794
|
Sweroside
|
CHEMBL456137
|
C049412
|
1 / 0 / 0 | No. 806 | No. 36 |
|
|
|
C00027252
|
3'-O-beta-D-glucopyranosylalangiside
/ (-)-3'-O-beta-D-glucopyranosylalangiside |
No. 1411 |
|
|||||
|
C00027254
|
6'-alpha-D-glucopyranosylalangiside
/ (-)-6'-alpha-D-glucopyranosylalangiside |
No. 1411 |
|
|||||
|
C00027255
|
6'-O-alpha-D-Xylopyranosylalangiside
/ (-)-6'-O-alpha-D-Xylopyranosylalangiside |
No. 1411 |
|
|||||
|
C00027256
|
6'-O-beta-D-glucopyranosylalangiside
/ (-)-6'-O-beta-D-glucopyranosylalangiside |
No. 1411 |
|
|||||
|
C00001805
|
Ankorine
|
No. 2276 | No. 4 |
|
||||
|
C00027270
|
Alangine
/ (-)-Alangine |
No. 2276 | No. 4 |
|
||||
|
C00027473
|
Protoemetinol
|
No. 2276 | No. 4 |
|
||||
|
C00027472
|
Protoemetine
|
No. 2276 | No. 4 |
|
||||
|
C00027481
|
Salsoline
/ (-)-O7-Methylsalsolinol |
CHEMBL1187592
CHEMBL1192723 CHEMBL1532461 |
C032837
|
3 / 4 / 3 | No. 2962 | No. 4 |
|
|
|
C00001794
|
Alamarine
|
No. 2972 |
|
|||||
|
C00001797
|
Alangimarine
|
No. 2972 |
|
|||||
|
C00027509
|
2'-O-trans-Sinapoylalangiside
|
No. 5314 |
|
|||||
|
C00027508
|
2'-O-trans-Feruloylalangiside
/ (-)-2'-O-trans-Feruloylalangiside |
No. 5314 |
|
| 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 |
| 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
|
| 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 | 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)
|