Metabolite

KNApSAcK Entry

id C00002487
Name PA 93 / U 6391 / Novo-R / Albamix / Cathocin / Inamycin / Robiocina / Albamycin / Cathomycin / Novobiocin / Sirbiocina / Stilbiocina / Cardelmycin / Spheromycin / Streptonivicin / Antibiotic PA-93 / Crystallinic acid
CAS RN 303-81-1
Standard InChI InChI=1S/C31H36N2O11/c1-14(2)7-8-16-13-17(9-11-19(16)34)27(37)33-21-22(35)18-10-12-20(15(3)24(18)42-28(21)38)41-29-23(36)25(43-30(32)39)26(40-6)31(4,5)44-29/h7,9-13,23,25-26,29,34-36H,8H2,1-6H3,(H2,32,39)(H,33,37)/t23-,25?,26+,29+/m0/s1
Standard InChI (Main Layer) InChI=1S/C31H36N2O11/c1-14(2)7-8-16-13-17(9-11-19(16)34)27(37)33-21-22(35)18-10-12-20(15(3)24(18)42-28(21)38)41-29-23(36)25(43-30(32)39)26(40-6)31(4,5)44-29/h7,9-13,23,25-26,29,34-36H,8H2,1-6H3,(H2,32,39)(H,33,37)

Cluster

Phytochemical cluster
KCF-S cluster No. 3473

Link

ChEMBL

By standard InChI
By standard InChI Main Layer CHEMBL35025 CHEMBL1237121 CHEMBL1617799 CHEMBL1619419 CHEMBL1625763 CHEMBL2221247

KEGG

By LinkDB C05080

CTD

By CAS RN D009675

Species

Summary

Plant class

class name count

Family

family name count
Streptomycetaceae 2

List (2)

* NCBI
KNApSAcK organism *ID *family *plant class *kingdom
Streptomyces niveus 193462 Streptomycetaceae Bacteria
Streptomyces spheroides 193462 Streptomycetaceae Bacteria

Human Protein / Gene in interaction

14 ChEMBL Protein in interactions

accession description class description compound assay ID (# of activities) # of diseases
(OMIM / KEGG)
Q9Y6L6 Solute carrier organic anion transporter family member 1B1 Electrochemical transporter CHEMBL1237121 CHEMBL2169429 (1)
1 / 0
O94956 Solute carrier organic anion transporter family member 2B1 Unclassified protein CHEMBL1237121 CHEMBL2169431 (1)
0 / 0
Q16543 Hsp90 co-chaperone Cdc37 Unclassified protein CHEMBL1237121 CHEMBL1803261 (1)
0 / 0
P02768 Serum albumin Secreted protein CHEMBL1237121 CHEMBL702885 (1) CHEMBL1661507 (1)
CHEMBL1661523 (1) CHEMBL1661524 (1)
CHEMBL1661525 (1) CHEMBL1661526 (1)
0 / 0
P11388 DNA topoisomerase 2-alpha Isomerase CHEMBL1237121 CHEMBL663891 (1) CHEMBL1785110 (1)
0 / 0
Q8TCC7 Solute carrier family 22 member 8 Antiporter CHEMBL1237121 CHEMBL1743167 (1)
0 / 0
Q4U2R8 Solute carrier family 22 member 6 Antiporter CHEMBL1237121 CHEMBL1743166 (1)
0 / 0
Q9NPD5 Solute carrier organic anion transporter family member 1B3 Electrochemical transporter CHEMBL1237121 CHEMBL2169430 (1)
1 / 0
Q9UNQ0 ATP-binding cassette sub-family G member 2 ATP binding cassette CHEMBL1237121 CHEMBL974473 (1) CHEMBL1047706 (1)
CHEMBL1047707 (1) CHEMBL2075183 (1)
CHEMBL2075596 (1) CHEMBL2076815 (1)
2 / 0
P08238 Heat shock protein HSP 90-beta Other cytosolic protein CHEMBL1237121 CHEMBL1664649 (1) CHEMBL1664650 (1)
CHEMBL1664651 (1) CHEMBL1664652 (1)
CHEMBL1664660 (1) CHEMBL1664668 (1)
CHEMBL1775390 (1)
0 / 0
Q02880 DNA topoisomerase 2-beta Isomerase CHEMBL1237121 CHEMBL663891 (1) CHEMBL686753 (1)
0 / 0
P22309 UDP-glucuronosyltransferase 1-1 Enzyme CHEMBL1237121 CHEMBL1908080 (1)
5 / 1
P07900 Heat shock protein HSP 90-alpha Other cytosolic protein CHEMBL1237121 CHEMBL1664661 (1)
0 / 0
Q96KQ7 Histone-lysine N-methyltransferase EHMT2 Enzyme CHEMBL1237121 CHEMBL1738442 (1)
0 / 0

CTD interaction (3)

compound gene gene name gene description interaction interaction type form reference
pmid
D009675 952 CD38
T10
CD38 molecule (EC:3.2.2.5) Novobiocin results in increased expression of CD38 mRNA increases expression
mRNA 11853877
D009675 952 CD38
T10
CD38 molecule (EC:3.2.2.5) Novobiocin results in increased expression of CD38 protein increases expression
protein 11853877
D009675 1000 CDH2
CD325
CDHN
CDw325
NCAD
cadherin 2, type 1, N-cadherin (neuronal) Novobiocin results in decreased expression of CDH2 protein decreases expression
protein 11853877

Related Disease

Diseases related to proteins in ChEMBL interactions

OMIM (8)

OMIM preferred title UniProt
#601816 Bilirubin, serum level of, quantitative trait locus 1; biliqtl1 P22309
#614490 Blood group, junior system; jr Q9UNQ0
#218800 Crigler-najjar syndrome, type i P22309
#606785 Crigler-najjar syndrome, type ii P22309
#143500 Gilbert syndrome P22309
#237450 Hyperbilirubinemia, rotor type; hblrr Q9NPD5
Q9Y6L6
#237900 Hyperbilirubinemia, transient familial neonatal; hblrtfn P22309
#138900 Uric acid concentration, serum, quantitative trait locus 1; uaqtl1 Q9UNQ0

KEGG DISEASE (1)

KEGG disease name UniProt
H00208 Hyperbilirubinemia P22309 (related)

Diseases related to CTD interactions

1 disease from interactions of metabolites

MeSH disease OMIM compound disease name evidence type reference
pmid
D008545 D009675 Melanoma therapeutic
1739614