PCIDB

KNApSAcK Metabolite C00027106

Metabolite

KNApSAcK Entry

id C00027106
Name Brassinin
CAS RN 105748-59-2
Standard InChI InChI=1S/C11H12N2S2/c1-15-11(14)13-7-8-6-12-10-5-3-2-4-9(8)10/h2-6,12H,7H2,1H3,(H,13,14)
Standard InChI (Main Layer) InChI=1S/C11H12N2S2/c1-15-11(14)13-7-8-6-12-10-5-3-2-4-9(8)10/h2-6,12H,7H2,1H3,(H,13,14)

Cluster

Phytochemical cluster
KCF-S cluster No. 3839

Link

ChEMBL

By standard InChI CHEMBL373777
By standard InChI Main Layer CHEMBL373777 CHEMBL1673034 CHEMBL1673036 CHEMBL1673037

KEGG

By LinkDB

CTD

By CAS RN C089020

Human Protein / Gene in interaction

5 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P14902 Indoleamine 2,3-dioxygenase 1 Enzyme CHEMBL373777 CHEMBL865155 (1) CHEMBL1670752 (1)
CHEMBL2343392 (1)
0 / 0
P10636 Microtubule-associated protein tau Unclassified protein CHEMBL373777 CHEMBL1614502 (1)
4 / 3
Q9UBT6 DNA polymerase kappa Enzyme CHEMBL373777 CHEMBL1794536 (1)
0 / 0
O00255 Menin Unclassified protein CHEMBL373777 CHEMBL1614257 (2)
2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme CHEMBL373777 CHEMBL1614257 (2)
1 / 3

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#145000 Hyperparathyroidism 1; hrpt1 O00255
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (10)

KEGG disease 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)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00001 Acute lymphoblastic leukemia (ALL) (precursor B lymphoblastic leukemia) Q03164 (related)
Q03164 (marker)
H00002 Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia) Q03164 (related)