General Information of Drug (ID: DMVR628)

Drug Name
Vindesine Drug Info
Synonyms
DAVA; Vindesin; Vindesina; Vindesinum; Desacetylvinblastine amide; Lilly 112531; Vindesina [INN-Spanish]; Vindesinum [INN-Latin]; Vindesine (USAN/INN); Vindesine [USAN:BAN:INN]; Vindesine [USAN:INN:BAN]; 3-(Aminocarbonyl)-O(sup 4)-deacetyl-3-de(methoxycarbonyl)vincaleukoblastine; 3-(aminocarbonyl)-O(4)-deacetyl-3-de(methoxycarbonyl)vincaleukoblastine; 3-Carbamoyl-4-deacetyl-3-de(methoxycarbonyl)vincaleukoblastine; 3-carbamoyl-O(4)-deacetyl-3-de(methoxycarbonyl)vincaleukoblastine; Methyl (5S,7S,9S)-9-[(2b,3b,4b,5a,12b,19a)-3-carbamoyl-3,4-dihydroxy-16-methoxy-1-methyl-6,7-didehydroaspidospermidin-15-yl]-5-ethyl-5-hydroxy-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indole-9-carboxylate; Methyl (5S,7S,9S)-9-[(2beta,3beta,4beta,5alpha,12beta,19alpha)-3-carbamoyl-3,4-dihydroxy-16-methoxy-1-methyl-6,7-didehydroaspidospermidin-15-yl]-5-ethyl-5-hydroxy-1,4,5,6,7,8,9,10-octahydro-2H-3,7-methanoazacycloundecino[5,4-b]indole-9-carboxylate
Therapeutic ClassAnticancer Agents
Cross-matching ID
PubChem CID
40839
ChEBI ID
CHEMBL36373
CAS Number
CAS 53643-48-4
TTD Drug ID
D04RLY
VARIDT Drug ID
DR00397
INTEDE Drug ID
DR1693

Consensus Signature of Drug Pharmacogenomic Perturbation (DPP)

Term Name NES FDR q-val Tag % Leading Edge Genes
Peroxisome -1.58 4.99e-2 72/82 (87.8%) AGXT;ABCD2;PEX10;...
Primary bile acid biosynthesis -1.62 4.12e-2 15/17 (88.24%) BAAT;AKR1C4;ACOT8;...
Thiamine metabolism -1.63 3.96e-2 12/15 (80%) ALPG;AK1;NFS1;...
Folate biosynthesis -1.66 3.12e-2 23/26 (88.46%) FPGS;ALPG;MOCS2;...
Sulfur relay system -1.66 3.02e-2 5/8 (62.5%) MOCS2;NFS1;TST
Glyoxylate and dicarboxylate metabolism -1.68 2.90e-2 23/30 (76.67%) GLUL;CS;AMT;...
Lysine degradation -1.76 1.13e-2 51/63 (80.95%) ACAT1;BBOX1;ALDH9A1;...
Glycine, serine and threonine metabolism -1.77 1.16e-2 31/40 (77.5%) BPGM;AMT;GCAT;...
Ribosome -1.78 1.12e-2 113/158 (71.52%) RPS4X;RPS29;RPL4;...
Mismatch repair -1.79 1.15e-2 22/23 (95.65%) POLD4;POLD3;RFC4;...
Steroid hormone biosynthesis -1.79 1.27e-2 43/61 (70.49%) HSD3B1;CYP1B1;CYP2E1;...
Fatty acid degradation -1.81 1.06e-2 40/43 (93.02%) HADHB;ACAT1;ACAA2;...
Citrate cycle (TCA cycle) -1.87 3.96e-3 30/30 (100%) FH;ACLY;SUCLG2;...
Valine, leucine and isoleucine degradation -1.93 0.00e+0 42/48 (87.5%) ACAD8;HADHB;IVD;...
Diabetic cardiomyopathy -1.93 0.00e+0 162/203 (79.8%) TGFBR2;COX4I1;NDUFS8;...
Propanoate metabolism -1.96 0.00e+0 30/34 (88.24%) ACAT1;DBT;EHHADH;...
Metabolism of xenobiotics by cytochrome P450 -2.01 0.00e+0 49/77 (63.64%) HPGDS;ADH7;CYP1B1;...
One carbon pool by folate -2.02 0.00e+0 15/20 (75%) AMT;ATIC;MTR;...
Oxidative phosphorylation -2.16 0.00e+0 93/133 (69.92%) COX4I1;NDUFS8;LHPP;...
DNA replication -2.19 0.00e+0 34/36 (94.44%) PRIM2;POLD4;POLD3;...
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Pharmacogenomic Perturbation Across Diseases and Tissues

Breast
Breast adenocarcinoma
Cell Line Name Cellosaurus Accession Species of Origin Drug Dosage Time Point Details
MCF7 CVCL_0031 Homo sapiens 10uM 6H, 24H
Colon
Colorectal adenocarcinoma
Cell Line Name Cellosaurus Accession Species of Origin Drug Dosage Time Point Details
HT-29 CVCL_0320 Homo sapiens 10uM 6H
Kidney
Normal (Immortalized)
Cell Line Name Cellosaurus Accession Species of Origin Drug Dosage Time Point Details
HA1E CVCL_0284 Homo sapiens 10uM 6H
Liver
Hepatocellular carcinoma
Cell Line Name Cellosaurus Accession Species of Origin Drug Dosage Time Point Details
HuH-7 CVCL_0336 Homo sapiens 4uM 72H
Lung
Lung adenocarcinoma
Cell Line Name Cellosaurus Accession Species of Origin Drug Dosage Time Point Details
A549 CVCL_0023 Homo sapiens 10uM 6H, 24H
Prostate
Prostate carcinoma
Cell Line Name Cellosaurus Accession Species of Origin Drug Dosage Time Point Details
PC-3 CVCL_0035 Homo sapiens 10uM 6H, 24H
VCaP CVCL_2235 Homo sapiens 10uM 6H, 24H
Skin
Melanoma
Cell Line Name Cellosaurus Accession Species of Origin Drug Dosage Time Point Details
A-375 CVCL_0132 Homo sapiens 10uM 6H