Species

KNApSAcK Entry

Organism name Lithospermum erythrorhizon
Genus Lithospermum
Family Boraginaceae
Kingdom Plantae

NCBI taxonomy

Entry

Linked NCBI taxonomy name Lithospermum erythrorhizon
Linked NCBI taxonomy ID 34254
Linked level species

Family

Family in NCBI taxonomy Boraginaceae
ID 21571

Kingdom (Superkingdom)

Kingdom (Superkingdom) in NCBI taxonomy Viridiplantae
ID 33090

Plant class

Plant class asterids
ID 71274

Natural Activity

List (28)

Species Activity
Lithospermum erythrorhizon Siebold & Zucc. Analgesic
Lithospermum erythrorhizon Siebold & Zucc. Anti-HIV
Lithospermum erythrorhizon Siebold & Zucc. Antiangiogenic
Lithospermum erythrorhizon Siebold & Zucc. Antibacterial
Lithospermum erythrorhizon Siebold & Zucc. Anticancer
Lithospermum erythrorhizon Siebold & Zucc. Antigonadotropic
Lithospermum erythrorhizon Siebold & Zucc. Antihyperthyroid
Lithospermum erythrorhizon Siebold & Zucc. Antiinflammatory
Lithospermum erythrorhizon Siebold & Zucc. Antimutagenic
Lithospermum erythrorhizon Siebold & Zucc. Antioxidant
Lithospermum erythrorhizon Siebold & Zucc. Antipyretic
Lithospermum erythrorhizon Siebold & Zucc. Antisarcomic
Lithospermum erythrorhizon Siebold & Zucc. Antiseptic
Lithospermum erythrorhizon Siebold & Zucc. Antithyroid
Lithospermum erythrorhizon Siebold & Zucc. Antitumor
Lithospermum erythrorhizon Siebold & Zucc. Antiviral
Lithospermum erythrorhizon Siebold & Zucc. Apoptotic
Lithospermum erythrorhizon Siebold & Zucc. Candidicide
Lithospermum erythrorhizon Siebold & Zucc. Circulostimulant
Lithospermum erythrorhizon Siebold & Zucc. Depurtive
Lithospermum erythrorhizon Siebold & Zucc. Detoxicant
Lithospermum erythrorhizon Siebold & Zucc. Diuretic
Lithospermum erythrorhizon Siebold & Zucc. Fungicide
Lithospermum erythrorhizon Siebold & Zucc. Granulant
Lithospermum erythrorhizon Siebold & Zucc. Hypoglycemic
Lithospermum erythrorhizon Siebold & Zucc. Immunomodulator
Lithospermum erythrorhizon Siebold & Zucc. Lactobacillacide
Lithospermum erythrorhizon Siebold & Zucc. Laxative

Metabolite list (12)

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
C00000856 External link 512 4-Hydroxybenzoic acid
/ p-Hydroxybenzoic acid
CHEMBL441343
C038193
21 / 7 / 16 2 / 1 No. 817 No. 81
C00031982 External link 512 Salvianolic acid B
/ Lithospermic acid B
CHEMBL1615434
C111702
No. 1276
C00030757 External link 512 Methyl linoleate
/ Methyl 9Z,12Z-octadecadienoate
C005575
No. 1785
C00030760 External link 512 Methyl oleate
/ Oleic acid methyl ester
/ Methyl (Z)-9-octadecenoate
CHEMBL465725
C005576
2 / 6 / 5 No. 1785
C00000859 External link 512 Shikonin
CHEMBL9470
CHEMBL29285
CHEMBL28457
16 / 14 / 12 No. 2968 No. 80
C00000846 External link 512 Geranyl diphosphate
/ Geranyl pyrophosphate
CHEMBL41342
C015234
1 / 0 / 0 2 / 0 No. 3475 No. 34
C00000852 External link 512 m-Geranyl-p-hydroxybenzoic acid
/ 3-Geranyl-4-hydroxybenzoic acid
CHEMBL482787
No. 4238
C00029462 External link 512 2-Methylpropanoic acid
CHEMBL108778
C020380
No. 4580
C00029461 External link 512 2-Methylbutanoic acid
CHEMBL1160012
CHEMBL1162482
CHEMBL1162483
2 / 1 / 2 No. 4580
C00029460 External link 512 2-Methyl-2-butenoic acid
CHEMBL55941
CHEMBL52416
C009489
No. 5138
C00001189 External link 512 Isovaleric acid
/ 3-Methylbutanoic acid
CHEMBL568737
C008216
4 / 0 No. 5262
C00040156 External link 512 Rhizonone
No. 7318

Human Protein / Gene in interactions

41 ChEMBL Protein in interactions

accession description class description KNApSAcK metabolite in interactions # of diseases
(OMIM / KEGG)
P10828 Thyroid hormone receptor beta NR1A2 C00000859 C00030760 3 / 1
O60656 UDP-glucuronosyltransferase 1-9 Enzyme C00000856 0 / 0
Q16637 Survival motor neuron protein Unclassified protein C00000859 4 / 1
Q9HAW8 UDP-glucuronosyltransferase 1-10 Enzyme C00000856 0 / 0
Q9Y2D0 Carbonic anhydrase 5B, mitochondrial Lyase C00000856 0 / 0
P35218 Carbonic anhydrase 5A, mitochondrial Lyase C00000856 0 / 0
P43166 Carbonic anhydrase 7 Lyase C00000856 0 / 0
P35610 Sterol O-acyltransferase 1 Enzyme C00000859 0 / 0
P51649 Succinate-semialdehyde dehydrogenase, mitochondrial Oxidoreductase C00000856 1 / 1
P00918 Carbonic anhydrase 2 Lyase C00000856 1 / 2
Q9UQ49 Sialidase-3 Enzyme C00000856 0 / 0
Q9HAW7 UDP-glucuronosyltransferase 1-7 Enzyme C00000856 0 / 0
P00533 Epidermal growth factor receptor TK tyrosine-protein kinase EGFR subfamily C00000856 1 / 8
P11387 DNA topoisomerase 1 Isomerase C00000859 0 / 0
P11473 Vitamin D3 receptor NR1I1 C00000859 2 / 3
P23280 Carbonic anhydrase 6 Lyase C00000856 0 / 0
Q9ULX7 Carbonic anhydrase 14 Lyase C00000856 0 / 0
P00352 Retinal dehydrogenase 1 Enzyme C00000859 0 / 0
O43570 Carbonic anhydrase 12 Lyase C00000856 1 / 2
Q92830 Histone acetyltransferase KAT2A Enzyme C00000859 0 / 0
P18031 Tyrosine-protein phosphatase non-receptor type 1 Tyr C00000859 0 / 0
P00915 Carbonic anhydrase 1 Lyase C00000856 0 / 0
O75908 Sterol O-acyltransferase 2 Enzyme C00000859 0 / 0
P14324 Farnesyl pyrophosphate synthase Transferase C00000846 0 / 0
P80404 4-aminobutyrate aminotransferase, mitochondrial Transferase C00000856 1 / 1
Q7Z4W1 L-xylulose reductase Enzyme C00029461 0 / 1
Q16790 Carbonic anhydrase 9 Lyase C00000856 0 / 1
Q9HAW9 UDP-glucuronosyltransferase 1-8 Enzyme C00000856 0 / 0
P51580 Thiopurine S-methyltransferase Enzyme C00000856 1 / 1
P27695 DNA-(apurinic or apyrimidinic site) lyase Enzyme C00000859 0 / 0
P10636 Microtubule-associated protein tau Unclassified protein C00000859 4 / 3
P19224 UDP-glucuronosyltransferase 1-6 Enzyme C00000856 0 / 0
P10275 Androgen receptor NR3C4 C00030760 3 / 4
P07451 Carbonic anhydrase 3 Lyase C00000856 0 / 0
P22748 Carbonic anhydrase 4 Lyase C00000856 1 / 1
Q9UBT6 DNA polymerase kappa Enzyme C00000859 0 / 0
P46063 ATP-dependent DNA helicase Q1 Enzyme C00000859 0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme C00000859 0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein C00000859 0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein C00000859 1 / 4
Q13148 TAR DNA-binding protein 43 Unclassified protein C00029461 1 / 1

8 Gene in CTD interactions

gene gene name gene description KNApSAcK metabolite in interactions
54575 UGT1A10, UDPGT, UGT-1J, UGT1-10, UGT1.10, UGT1J UDP glucuronosyltransferase 1 family, polypeptide A10 (EC:2.4.1.17) C00001189
54659 UGT1A3, UDPGT, UDPGT_1-3, UGT-1C, UGT1-03, UGT1.3, UGT1C UDP glucuronosyltransferase 1 family, polypeptide A3 (EC:2.4.1.17) C00001189
54577 UGT1A7, UDPGT, UDPGT_1-7, UGT-1G, UGT1-07, UGT1.7, UGT1G UDP glucuronosyltransferase 1 family, polypeptide A7 (EC:2.4.1.17) C00001189
54576 UGT1A8, UDPGT, UDPGT_1-8, UGT-1H, UGT1-08, UGT1.8, UGT1A8S, UGT1H UDP glucuronosyltransferase 1 family, polypeptide A8 (EC:2.4.1.17) C00001189
3156 HMGCR, LDLCQ3 3-hydroxy-3-methylglutaryl-CoA reductase (EC:1.1.1.34) C00000846
5906 RAP1A, KREV-1, KREV1, RAP1, SMGP21 RAP1A, member of RAS oncogene family C00000846
3952 LEP, LEPD, OB, OBS leptin C00000856
6817 SULT1A1, HAST1/HAST2, P-PST, PST, ST1A1, ST1A3, STP, STP1, TSPST1 sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1 (EC:2.8.2.1) C00000856

Related Diseases

Diseases related to proteins in ChEMBL interactions

OMIM (25)

OMIM preferred title UniProt
#612069 Amyotrophic lateral sclerosis 10, with or without frontotemporal dementia; als10 Q13148
#300068 Androgen insensitivity syndrome; ais P10275
#312300 Androgen insensitivity, partial; pais P10275
#600274 Frontotemporal dementia; ftd P10636
#613163 Gaba-transaminase deficiency P80404
#143860 Hyperchlorhidrosis, isolated O43570
#211980 Lung cancer P00533
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#259730 Osteopetrosis, autosomal recessive 3; optb3 P00918
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#600852 Retinitis pigmentosa 17; rp17 P22748
#313200 Spinal and bulbar muscular atrophy, x-linked 1; smax1 P10275
#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
#271980 Succinic semialdehyde dehydrogenase deficiency; ssadhd P51649
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#610460 Thiopurine s-methyltransferase deficiency P51580
#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 (33)

KEGG name UniProt
H01302 Hyperchlorhidrosis isolated (HCHLH) O43570 (related)
H00021 Renal cell carcinoma O43570 (marker)
Q16790 (marker)
H00016 Oral cancer P00533 (related)
P00533 (marker)
H00017 Esophageal cancer P00533 (related)
H00018 Gastric cancer P00533 (related)
H00022 Bladder cancer P00533 (related)
H00028 Choriocarcinoma P00533 (related)
H00030 Cervical cancer P00533 (related)
H00042 Glioma P00533 (related)
P00533 (marker)
H00055 Laryngeal cancer P00533 (related)
P00533 (marker)
H00241 Combined proximal and distal renal tubular acidosis (RTA type 3) P00918 (related)
H00436 Osteopetrosis P00918 (related)
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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
Q13148 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
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)
H00527 Retinitis pigmentosa (RP) P22748 (related)
H00964 Thiopurine S-methyltransferase deficiency (TPMT deficiency) P51580 (related)
H00835 Succinic semialdehyde dehydrogenase (SSADH) deficiency P51649 (related)
H01257 GABA-transaminase deficiency P80404 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q01196 (related)
Q01196 (marker)
H00003 Acute myeloid leukemia (AML) Q01196 (related)
Q01196 (marker)
Q13951 (marker)
H00004 Chronic myeloid leukemia (CML) Q01196 (related)
H00978 Thrombocytopenia (THC) Q01196 (related)
H00455 Spinal muscular atrophy (SMA) Q16637 (related)
H01065 Pentosuria Q7Z4W1 (related)

Diseases related to CTD interactions

1 disease in interactions with metabolites

MESH or OMIM name KNApSAcK
metabolite
D012220 Rhinitis C00000856