Species

KNApSAcK Entry

Organism name Larix kaempferi (Lamb.) Carr
Genus Larix
Family Pinaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Larix
Linked NCBI taxonomy ID 3325
Linked level genus

Family

Family in NCBI taxonomy Pinaceae
ID 3318

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class Spermatophyta
ID 58024

Metabolite list (15)

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
C00023770 External link 512 Sitosterol
/ Stigmasta-5,22-dien-3beta-ol
/ (24R)24-Ethylcholesta-5,22-dien-3beta-ol
CHEMBL221542
CHEMBL1398443
CHEMBL1875388
17 / 19 / 12 No. 53 No. 11
C00029821 External link 512 Sitostenone
/ beta-Sitostenone
/ Stigmast-4-en-3-one
/ Stigmast-4-ene-3-one
CHEMBL66926
No. 53 No. 11
C00041127 External link 512 Stigmastan 3,6-dione
No. 68 No. 11
C00041128 External link 512 Stigmastan-3-one
No. 68 No. 11
C00003747 External link 512 Friedelin
/ Friedeline
/ Friedelanone
/ (-)-Friedelin
/ Friedelan-3-one
CHEMBL485998
CHEMBL1551590
C060796
2 / 0 / 0 No. 101 No. 52
C00035217 External link 512 24-Methylenecycloartanone
/ 3-Oxo-24-methylenecycloartane
CHEMBL376835
No. 129 No. 11
C00003661 External link 512 24-Methylenecycloartanol
/ 24-Methylenecycloartan-3beta-ol
CHEMBL121329
CHEMBL376350
C066041
No. 129 No. 11
C00040804 External link 512 24-Methylenecycloartan-3-one
CHEMBL376835
No. 129 No. 11
C00020065 External link 512 alpha-Cadinol
/ (-)-alpha-Cadinol
CHEMBL486795
No. 205 No. 38
C00022713 External link 512 Larixol
CHEMBL1370284
5 / 7 / 37 No. 256 No. 46
C00040773 External link 512 16-nor-15-Oxoabieta-8,11,13-trien-18-oic acid
No. 323 No. 41
C00040763 External link 512 12,15-Dihydroxyabieta-8,11,13-trien-18-oic acid
No. 323 No. 41
C00040858 External link 512 Abieta-8,11,13,15-tetraen-18-oic acid
No. 323 No. 41
C00020240 External link 512 Oplopanone
/ (-)-Oplopanone
No. 1395
C00041092 External link 512 Rheosmin
CHEMBL105912
C035522
1 / 3 / 4 1 / 1 No. 5516

Human Protein / Gene in interactions

24 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P08684 Cytochrome P450 3A4 Cytochrome P450 3A4 C00022713 C00023770 0 / 1
P00734 Prothrombin S1A C00023770 4 / 2
P04637 Cellular tumor antigen p53 Transcription Factor C00022713 7 / 37
P49798 Regulator of G-protein signaling 4 Unclassified protein C00023770 2 / 0
P06746 DNA polymerase beta Enzyme C00023770 0 / 0
Q8TDU6 G-protein coupled bile acid receptor 1 Steroid-like ligand receptor C00003747 0 / 0
P08047 Transcription factor Sp1 Unclassified protein C00023770 0 / 0
P16473 Thyrotropin receptor Glycohormone receptor C00023770 3 / 2
P08183 Multidrug resistance protein 1 drug C00023770 1 / 0
P11712 Cytochrome P450 2C9 Cytochrome P450 2C9 C00023770 0 / 1
P49841 Glycogen synthase kinase-3 beta Gsk C00023770 0 / 0
O94782 Ubiquitin carboxyl-terminal hydrolase 1 Enzyme C00022713 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00023770 0 / 0
P14679 Tyrosinase Oxidoreductase C00023770 4 / 2
Q96RI1 Bile acid receptor NR1H4 C00003747 0 / 0
P28482 Mitogen-activated protein kinase 1 Erk C00022713 0 / 0
P05177 Cytochrome P450 1A2 Cytochrome P450 1A2 C00023770 0 / 0
P03372 Estrogen receptor NR3A1 C00023770 1 / 1
P16050 Arachidonate 15-lipoxygenase Enzyme C00022713 0 / 0
P33261 Cytochrome P450 2C19 Cytochrome P450 2C19 C00023770 1 / 1
P10635 Cytochrome P450 2D6 Cytochrome P450 2D6 C00023770 1 / 0
P10275 Androgen receptor NR3C4 C00041092 3 / 4
P80365 Corticosteroid 11-beta-dehydrogenase isozyme 2 Enzyme C00023770 1 / 1
Q9NUW8 Tyrosyl-DNA phosphodiesterase 1 Enzyme C00023770 1 / 1

1 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
367 AR, AIS, DHTR, HUMARA, HYSP1, KD, NR3C4, SBMA, SMAX1, TFM androgen receptor C00041092

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (29)

OMIM preferred title UniProt
#202300 Adrenocortical carcinoma, hereditary; adcc P04637
#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
#614740 Basal cell carcinoma, susceptibility to, 7; bcc7 P04637
#609535 Drug metabolism, poor, cyp2c19-related P33261
#608902 Drug metabolism, poor, cyp2d6-related P10635
#133239 Esophageal cancer P04637
#615363 Estrogen resistance; estrr P03372
#603373 Hyperthyroidism, familial gestational P16473
#609152 Hyperthyroidism, nonautoimmune P16473
#275200 Hypothyroidism, congenital, nongoitrous, 1; chng1 P16473
#612244 Inflammatory bowel disease 13; ibd13 P08183
#151623 Li-fraumeni syndrome 1; lfs1 P04637
#211980 Lung cancer P04637
#260500 Papilloma of choroid plexus; cpp P04637
#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
#275355 Squamous cell carcinoma, head and neck; hnscc P04637
#601367 Stroke, ischemic P00734
#188050 Thrombophilia due to thrombin defect; thph1 P00734

KEGG DISEASE (50)

KEGG name UniProt
H00223 Inherited thrombophilia P00734 (related)
H01254 Congenital prothrombin deficiency P00734 (related)
H00026 Endometrial Cancer P03372 (marker)
P04637 (related)
H00004 Chronic myeloid leukemia (CML) P04637 (related)
H00005 Chronic lymphocytic leukemia (CLL) P04637 (related)
H00006 Hairy-cell leukemia P04637 (related)
H00008 Burkitt lymphoma P04637 (related)
H00009 Adult T-cell leukemia P04637 (related)
H00010 Multiple myeloma P04637 (related)
H00013 Small cell lung cancer P04637 (related)
H00014 Non-small cell lung cancer P04637 (related)
H00015 Malignant pleural mesothelioma P04637 (related)
H00016 Oral cancer P04637 (related)
P04637 (marker)
H00017 Esophageal cancer P04637 (related)
P04637 (marker)
H00018 Gastric cancer P04637 (related)
H00019 Pancreatic cancer P04637 (related)
P04637 (marker)
H00020 Colorectal cancer P04637 (related)
P04637 (marker)
H00022 Bladder cancer P04637 (related)
H00025 Penile cancer P04637 (related)
P04637 (marker)
H00027 Ovarian cancer P04637 (related)
H00028 Choriocarcinoma P04637 (related)
H00029 Vulvar cancer P04637 (related)
H00031 Breast cancer P04637 (related)
H00032 Thyroid cancer P04637 (related)
H00033 Adrenal carcinoma P04637 (related)
H00036 Osteosarcoma P04637 (related)
P08684 (marker)
H00038 Malignant melanoma P04637 (related)
P14679 (marker)
H00039 Basal cell carcinoma P04637 (related)
H00040 Squamous cell carcinoma P04637 (related)
H00041 Kaposi's sarcoma P04637 (related)
H00042 Glioma P04637 (related)
P04637 (marker)
H00044 Cancer of the anal canal P04637 (related)
H00046 Cholangiocarcinoma P04637 (related)
H00047 Gallbladder cancer P04637 (related)
H00048 Hepatocellular carcinoma P04637 (related)
H00055 Laryngeal cancer P04637 (related)
P04637 (marker)
H00881 Li-Fraumeni syndrome P04637 (related)
H01007 Choroid plexus papilloma P04637 (related)
H00021 Renal cell carcinoma P04637 (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)
H01205 Coumarin resistance P11712 (related)
H00168 Oculocutaneous albinism (OCA) P14679 (related)
H00250 Congenital nongoitrous hypothyroidism (CHNG) P16473 (related)
H01269 Congenital hyperthyroidism P16473 (related)
H01171 Poor drug metabolism (PM) P33261 (related)
H00259 Apparent mineralocorticoid excess syndrome P80365 (related)
H00063 Spinocerebellar ataxia (SCA) Q9NUW8 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D009765 Obesity C00041092