Metabolite

KNApSAcK Entry

id C00003133
Name Fumidil / Fugillin / Fumadil B / Amebacilin / Fumagillin / Fumagillin DCH / (-)-Fumagillin
CAS RN 23110-15-8
Standard InChI InChI=1S/C26H34O7/c1-18(2)13-14-20-25(3,33-20)24-23(30-4)19(15-16-26(24)17-31-26)32-22(29)12-10-8-6-5-7-9-11-21(27)28/h5-13,19-20,23-24H,14-17H2,1-4H3,(H,27,28)/b7-5+,8-6+,11-9+,12-10+/t19-,20-,23-,24-,25+,26+/m1/s1
Standard InChI (Main Layer) InChI=1S/C26H34O7/c1-18(2)13-14-20-25(3,33-20)24-23(30-4)19(15-16-26(24)17-31-26)32-22(29)12-10-8-6-5-7-9-11-21(27)28/h5-13,19-20,23-24H,14-17H2,1-4H3,(H,27,28)

Cluster

Phytochemical cluster
KCF-S cluster No. 2065

Link

ChEMBL

By standard InChI CHEMBL32838
By standard InChI Main Layer CHEMBL32838 CHEMBL117603 CHEMBL1396346 CHEMBL1522710 CHEMBL1992691

KEGG

By LinkDB C09668

CTD

By CAS RN C026211

Species

Summary

Plant class

class name count

Family

family name count
Aspergillaceae 2

List (2)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Aspergillus fumigatus 746128 Aspergillaceae Fungi
Penicillium janczewskii 121612 Aspergillaceae Fungi

Human Protein / Gene in interaction

13 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q03181 Peroxisome proliferator-activated receptor delta NR1C2 CHEMBL32838 CHEMBL1794552 (1)
0 / 0
P02545 Prelamin-A/C Unclassified protein CHEMBL1396346 CHEMBL1614544 (1)
11 / 10
P11473 Vitamin D3 receptor NR1I1 CHEMBL1396346 CHEMBL1522710 CHEMBL1794311 (2)
2 / 3
P00352 Retinal dehydrogenase 1 Enzyme CHEMBL1522710 CHEMBL1614458 (1)
0 / 0
O75496 Geminin Unclassified protein CHEMBL1396346 CHEMBL2114843 (1) CHEMBL2114780 (1)
0 / 0
P53582 Methionine aminopeptidase 1 M24A CHEMBL32838 CHEMBL1027136 (1)
0 / 0
P10636 Microtubule-associated protein tau Unclassified protein CHEMBL1522710 CHEMBL1614250 (1) CHEMBL1614421 (1)
4 / 3
Q16236 Nuclear factor erythroid 2-related factor 2 Unclassified protein CHEMBL32838 CHEMBL2114890 (1)
0 / 0
P50579 Methionine aminopeptidase 2 M24A CHEMBL32838 CHEMBL117603 CHEMBL709685 (1) CHEMBL716777 (1)
CHEMBL881950 (1) CHEMBL1027137 (1)
CHEMBL1048165 (1)
0 / 0
Q9UBT6 DNA polymerase kappa Enzyme CHEMBL1522710 CHEMBL1794536 (1)
0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme CHEMBL1396346 CHEMBL1522710 CHEMBL1738442 (2)
0 / 0
O00255 Menin Unclassified protein CHEMBL1522710 CHEMBL1614531 (1)
2 / 5
Q03164 Histone-lysine N-methyltransferase 2A Enzyme CHEMBL1522710 CHEMBL1614531 (1)
1 / 3

CTD interaction (5)

compound gene gene name gene description interaction interaction type form reference
pmid
C026211 23173 METAP1
MAP1A
MetAP1A
methionyl aminopeptidase 1 (EC:3.4.11.18) fumagillin results in decreased activity of METAP1 protein decreases activity
protein 14534293
C026211 23173 METAP1
MAP1A
MetAP1A
methionyl aminopeptidase 1 (EC:3.4.11.18) [fumagillin results in decreased activity of [METAP1 protein co-treated with METAP2 protein]] which results in decreased metabolism of YWHAG protein affects cotreatment
/ decreases activity
/ decreases metabolic processing
protein 14534293
C026211 10988 METAP2
MAP2
MNPEP
p67
p67eIF2
methionyl aminopeptidase 2 (EC:3.4.11.18) [fumagillin results in decreased activity of [METAP1 protein co-treated with METAP2 protein]] which results in decreased metabolism of YWHAG protein affects cotreatment
/ decreases activity
/ decreases metabolic processing
protein 14534293
C026211 10988 METAP2
MAP2
MNPEP
p67
p67eIF2
methionyl aminopeptidase 2 (EC:3.4.11.18) fumagillin results in decreased activity of METAP2 protein decreases activity
protein 14534293
15516829
C026211 7532 YWHAG
14-3-3GAMMA
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide [fumagillin results in decreased activity of [METAP1 protein co-treated with METAP2 protein]] which results in decreased metabolism of YWHAG protein affects cotreatment
/ decreases activity
/ decreases metabolic processing
protein 14534293

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (20)

OMIM preferred title UniProt
#115200 Cardiomyopathy, dilated, 1a; cmd1a P02545
#212112 Cardiomyopathy, dilated, with hypergonadotropic hypogonadism P02545
#605588 Charcot-marie-tooth disease, axonal, type 2b1; cmt2b1 P02545
#181350 Emery-dreifuss muscular dystrophy 2, autosomal dominant; edmd2 P02545
#600274 Frontotemporal dementia; ftd P10636
#605130 Hairy elbows, short stature, facial dysmorphism, and developmental delay Q03164
#610140 Heart-hand syndrome, slovenian type P02545
#176670 Hutchinson-gilford progeria syndrome; hgps P02545
#145000 Hyperparathyroidism 1; hrpt1 O00255
#151660 Lipodystrophy, familial partial, type 2; fpld2 P02545
#248370 Mandibuloacral dysplasia with type a lipodystrophy; mada P02545
#131100 Multiple endocrine neoplasia, type i; men1 O00255
#613205 Muscular dystrophy, congenital, lmna-related P02545
#159001 Muscular dystrophy, limb-girdle, type 1b; lgmd1b P02545
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#275210 Restrictive dermopathy, lethal P02545
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (23)

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)
H00264 Charcot-Marie-Tooth disease (CMT) P02545 (related)
H00294 Dilated cardiomyopathy (DCM) P02545 (related)
H00420 Familial partial lipodystrophy (FPL) P02545 (related)
H00563 Emery-Dreifuss muscular dystrophy P02545 (related)
H00590 Congenital muscular dystrophies (CMD/MDC) P02545 (related)
H00593 Limb-girdle muscular dystrophy (LGMD) P02545 (related)
H00601 Hutchinson-Gilford progeria syndrome P02545 (related)
H00663 Restrictive dermopathy P02545 (related)
H00665 Mandibuloacral dysplasia P02545 (related)
H01216 Left ventricular noncompaction (LVNC) P02545 (related)
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (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)

Diseases related to CTD interactions

3 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D009362 C026211 Neoplasm Metastasis therapeutic
15682466
D009389 C026211 Neovascularization, Pathologic therapeutic
15682466
D009765 C026211 Obesity therapeutic
20094042