Metabolite

KNApSAcK Entry

id C00027627
Name (+)-Curacin A
CAS RN 155233-30-0
Standard InChI InChI=1S/C23H35NOS/c1-5-11-21(25-4)15-14-18(2)12-9-7-6-8-10-13-20-17-26-23(24-20)22-16-19(22)3/h5,7,9-10,12-13,19-22H,1,6,8,11,14-17H2,2-4H3/b9-7+,13-10-,18-12+/t19-,20+,21-,22+/m0/s1
Standard InChI (Main Layer) InChI=1S/C23H35NOS/c1-5-11-21(25-4)15-14-18(2)12-9-7-6-8-10-13-20-17-26-23(24-20)22-16-19(22)3/h5,7,9-10,12-13,19-22H,1,6,8,11,14-17H2,2-4H3

Cluster

Phytochemical cluster
KCF-S cluster No. 5280

Link

ChEMBL

By standard InChI CHEMBL89138
By standard InChI Main Layer CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL508496 CHEMBL454328 CHEMBL2115069

KEGG

By LinkDB C11689

CTD

By CAS RN C095843

Species

Summary

Plant class

class name count

Family

family name count

List (1)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Lyngbya majuscula 158786 Bacteria

Human Protein / Gene in interaction

15 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q13748 Tubulin alpha-3C/D chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
0 / 0
P68366 Tubulin alpha-4A chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
0 / 0
Q9H4B7 Tubulin beta-1 chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
1 / 0
P04350 Tubulin beta-4A chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
2 / 0
Q3ZCM7 Tubulin beta-8 chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
0 / 0
P07437 Tubulin beta chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
0 / 0
Q71U36 Tubulin alpha-1A chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
1 / 1
P68371 Tubulin beta-4B chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
0 / 0
Q13509 Tubulin beta-3 chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
2 / 1
P68363 Tubulin alpha-1B chain Unclassified protein CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
0 / 0
Q13885 Tubulin beta-2A chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
0 / 0
Q6PEY2 Tubulin alpha-3E chain Unclassified protein CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
0 / 0
Q9BQE3 Tubulin alpha-1C chain Unclassified protein CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
0 / 0
Q9BUF5 Tubulin beta-6 chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
0 / 0
Q9BVA1 Tubulin beta-2B chain Structural CHEMBL55367 CHEMBL56708 CHEMBL58871 CHEMBL294667 CHEMBL57092 CHEMBL89138 CHEMBL2115069 CHEMBL622599 (7)
1 / 0

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (7)

OMIM preferred title UniProt
#614039 Cortical dysplasia, complex, with other brain malformations 1; cdcbm1 Q13509
#128101 Dystonia 4, torsion, autosomal dominant; dyt4 P04350
#600638 Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement; cfeom3a Q13509
#612438 Leukodystrophy, hypomyelinating, 6; hld6 P04350
#611603 Lissencephaly 3; lis3 Q71U36
#613112 Macrothrombocytopenia, autosomal dominant, tubb1-related Q9H4B7
#610031 Polymicrogyria, symmetric or asymmetric; pmgysa Q9BVA1

KEGG DISEASE (2)

KEGG disease name UniProt
H00838 Congenital fibrosis of the extraocular muscles (CFEOM) Q13509 (related)
H00268 Lissencephaly (LIS) Q71U36 (related)