Metabolite

KNApSAcK Entry

id C00018851
Name M 4365A2 / Rosamicin / Sch 14947 / NSC 175150 / Rosaramicin / Juvenimicin A3 / Antibiotic 67-694 / Antibiotic T 1124C / Antibiotic M 4365A2 / 4'-Deoxycirramycin A1
CAS RN 35834-26-5
Standard InChI InChI=1S/C31H51NO9/c1-9-25-20(5)29-31(6,41-29)12-10-23(34)17(2)14-21(11-13-33)28(19(4)24(35)16-26(36)39-25)40-30-27(37)22(32(7)8)15-18(3)38-30/h10,12-13,17-22,24-25,27-30,35,37H,9,11,14-16H2,1-8H3/b12-10+
Standard InChI (Main Layer) InChI=1S/C31H51NO9/c1-9-25-20(5)29-31(6,41-29)12-10-23(34)17(2)14-21(11-13-33)28(19(4)24(35)16-26(36)39-25)40-30-27(37)22(32(7)8)15-18(3)38-30/h10,12-13,17-22,24-25,27-30,35,37H,9,11,14-16H2,1-8H3

Cluster

Phytochemical cluster
KCF-S cluster No. 1715

Link

ChEMBL

By standard InChI CHEMBL1966403
By standard InChI Main Layer CHEMBL8965 CHEMBL26194 CHEMBL1546091 CHEMBL1966403 CHEMBL2357105

KEGG

By LinkDB

CTD

By CAS RN C060286

Species

Summary

Plant class

class name count

Family

family name count
Micromonosporaceae 1

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Micromonospora rosaria NRRL No. 3718 1873 Micromonosporaceae Bacteria

Human Protein / Gene in interaction

4 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q13315 Serine-protein kinase ATM Atypical serine/threonine protein kinase PIKK subfamily CHEMBL1546091 CHEMBL1614153 (1)
1 / 4
O75496 Geminin Unclassified protein CHEMBL26194 CHEMBL2114780 (1)
0 / 0
Q96QE3 ATPase family AAA domain-containing protein 5 Unclassified protein CHEMBL1546091 CHEMBL1738588 (1)
0 / 0
P10636 Microtubule-associated protein tau Unclassified protein CHEMBL1546091 CHEMBL1614421 (1)
4 / 3

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (5)

OMIM preferred title UniProt
#208900 Ataxia-telangiectasia; at Q13315
#600274 Frontotemporal dementia; ftd P10636
#260540 Parkinson-dementia syndrome P10636
#172700 Pick disease of brain P10636
#601104 Supranuclear palsy, progressive, 1; psnp1 P10636

KEGG DISEASE (7)

KEGG disease name UniProt
H00058 Amyotrophic lateral sclerosis (ALS) P10636 (related)
H00077 Progressive supranuclear palsy (PSP) P10636 (related)
H00078 Frontotemporal lobar degeneration (FTLD) P10636 (related)
H00005 Chronic lymphocytic leukemia (CLL) Q13315 (related)
H00064 Ataxia telangiectasia (AT) Q13315 (related)
H00094 DNA repair defects Q13315 (related)
H00848 Ataxia with ocular apraxia (AOA) Q13315 (related)