Metabolite

KNApSAcK Entry

id C00023903
Name Fusidic acid
CAS RN 6990-06-3
Standard InChI InChI=1S/C31H48O6/c1-17(2)9-8-10-20(28(35)36)26-22-15-24(34)27-29(5)13-12-23(33)18(3)21(29)11-14-30(27,6)31(22,7)16-25(26)37-19(4)32/h9,18,21-25,27,33-34H,8,10-16H2,1-7H3,(H,35,36)/b26-20-/t18-,21-,22-,23+,24+,25-,27-,29-,30-,31-/m0/s1
Standard InChI (Main Layer) InChI=1S/C31H48O6/c1-17(2)9-8-10-20(28(35)36)26-22-15-24(34)27-29(5)13-12-23(33)18(3)21(29)11-14-30(27,6)31(22,7)16-25(26)37-19(4)32/h9,18,21-25,27,33-34H,8,10-16H2,1-7H3,(H,35,36)

Cluster

Phytochemical cluster
KCF-S cluster No. 725

Link

ChEMBL

By standard InChI CHEMBL374975
By standard InChI Main Layer CHEMBL117110 CHEMBL383466 CHEMBL374975 CHEMBL1334456 CHEMBL1477084 CHEMBL1552107 CHEMBL1619349 CHEMBL1620692 CHEMBL1625992 CHEMBL2068923

KEGG

By LinkDB C06694

CTD

By CAS RN D005672

Species

Summary

Plant class

class name count

Family

family name count

List (5)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Acremonium fusidioides 749674 Fungi
Calcarisporium arbuscula 240499 Fungi
Cephalosporium acremonium 5044 Fungi
Gabarnaudia tholispora
Isaria kogane

Human Protein / Gene in interaction

10 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
P02768 Serum albumin Secreted protein CHEMBL374975 CHEMBL702885 (1) CHEMBL1661507 (1)
CHEMBL1661527 (1) CHEMBL1661528 (1)
CHEMBL1661529 (1)
0 / 0
P11473 Vitamin D3 receptor NR1I1 CHEMBL1334456 CHEMBL1794311 (1)
2 / 3
P39748 Flap endonuclease 1 Enzyme CHEMBL1477084 CHEMBL1794486 (1)
0 / 0
O75496 Geminin Unclassified protein CHEMBL1334456 CHEMBL2114843 (1)
0 / 0
P63092 Guanine nucleotide-binding protein G(s) subunit alpha isoforms short Other membrane protein CHEMBL1334456 CHEMBL2114817 (1)
7 / 3
P83916 Chromobox protein homolog 1 Unclassified protein CHEMBL1334456 CHEMBL1794401 (1)
0 / 0
Q92887 Canalicular multispecific organic anion transporter 1 Unclassified protein CHEMBL374975 CHEMBL1006005 (1)
1 / 1
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme CHEMBL1477084 CHEMBL1738442 (1)
0 / 0
Q13951 Core-binding factor subunit beta Unclassified protein CHEMBL1552107 CHEMBL1613933 (1)
0 / 1
Q01196 Runt-related transcription factor 1 Unclassified protein CHEMBL1552107 CHEMBL1613933 (1)
1 / 6

CTD interaction (1)

compound gene gene name gene description interaction interaction type form reference
pmid
D005672 8647 ABCB11
ABC16
BRIC2
BSEP
PFIC-2
PFIC2
PGY4
SPGP
ATP-binding cassette, sub-family B (MDR/TAP), member 11 Fusidic Acid results in decreased activity of ABCB11 protein decreases activity
protein 20829430

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (11)

OMIM preferred title UniProt
#219080 Acth-independent macronodular adrenal hyperplasia; aimah P63092
#237500 Dubin-johnson syndrome; djs Q92887
#174800 Mccune-albright syndrome; mas P63092
#607948 Mycobacterium tuberculosis, susceptibility to P11473
#166350 Osseous heteroplasia, progressive; poh P63092
#102200 Pituitary adenoma, growth hormone-secreting P63092
#601399 Platelet disorder, familial, with associated myeloid malignancy Q01196
#103580 Pseudohypoparathyroidism, type ia; php1a P63092
#603233 Pseudohypoparathyroidism, type ib; php1b P63092
#612462 Pseudohypoparathyroidism, type ic; php1c P63092
#277440 Vitamin d-dependent rickets, type 2a; vddr2a P11473

KEGG DISEASE (11)

KEGG disease name UniProt
H00342 Tuberculosis P11473 (related)
H00784 Localized autosomal recessive hypotrichosis P11473 (related)
H01143 Vitamin D-dependent rickets P11473 (related)
H00244 Pseudohypoparathyroidism P63092 (related)
H00441 Progressive osseous heteroplasia (POH) P63092 (related)
H00501 Fibrous dysplasia, polyostotic P63092 (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)
H00208 Hyperbilirubinemia Q92887 (related)

Diseases related to CTD interactions

14 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D058186 D005672 Acute Kidney Injury marker/mechanism
8394548
9287276
11823554
D000756 D005672 Anemia, Sideroblastic marker/mechanism
12602389
15059072
D002779 D005672 Cholestasis marker/mechanism
12148265
D003424 D005672 Crohn Disease therapeutic
1420741
D004697 D005672 Endocarditis, Bacterial therapeutic
16735427
D006932 D005672 Hyperbilirubinemia marker/mechanism
3608735
7244561
D006996 D005672 Hypocalcemia marker/mechanism
11823554
D007565 D005672 Jaundice marker/mechanism
6867701
12148265
D009325 D005672 Nausea marker/mechanism
1420741
D010019 D005672 Osteomyelitis therapeutic
3608735
11823554
D012206 D005672 Rhabdomyolysis marker/mechanism
18487263
20546290
D013203 D005672 Staphylococcal Infections therapeutic
5560145
12148265
18199793
19188393
D013924 D005672 Thrombophlebitis marker/mechanism
7244561
D014552 D005672 Urinary Tract Infections therapeutic
12148265