General Information of Drug (ID: DMB0VY8)

Drug Name
Pancuronium Drug Info
Synonyms
Mioblock; Pavulon; Bromure de pancuronium; Bromuro de pancuronio; PANCURONIUM BROMIDE; Pancuronii bromidum; Pancuronium dibromide; Poncuronium bromide; NA 97; ORG NA 97; P 1918; Bromure de pancuronium [INN-French]; Bromuro de pancuronio [INN-Spanish]; ORG-NA 97; Pancuronii bromidum [INN-Latin]; Pavulon (TN); Pancuronium bromide (JP15/USAN/INN); Pancuronium bromide [USAN:BAN:INN:JAN]; Piperidinium, 1,1'-(3alpha,17beta-dihydroxy-5alpha-androstan-2beta,16beta-ylene)bis(1-methyl-, dibromide, diacetate; Piperidinium, 1,1'-(3alpha,17beta-dihydroxy-5alpha-androstan-2beta,16beta-ylene)bis(1-methyl-, dibromide, diacetate (8CI); Piperidinium, 1,1'-((2beta,3alpha,5alpha,16beta,17beta)-3,17-bis(acetyloxy)androstane-2,16-diyl)bis(1-methyl)-, dibromide; Piperidinium, 1,1'-((2beta,3alpha,5alpha,16beta,17beta)-3,17-bis(acetyloxy)androstane-2,16-diyl)bis(1-methyl-, dibromide; Piperidinium, 1,1'-(2-beta,16-beta-(3-alpha,17-beta-dihydroxy-5-alpha-androstanylene))bis(1-methyl-, dibromide, diacetate; Piperidinium, 1,1'-[(2.beta.,3.alpha.,5.alpha.,16.beta.,17.beta.)-3,17-bis(acetyloxy)androstane-2,16-diyl]bis[1-methyl-, dibromide; (2beta,3alpha,5alpha,16beta,17beta)-3,17-bis(acetyloxy)-2,16-bis(1-methylpiperidinium-1-yl)androstane dibromide; [(2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-17-acetyloxy-10,13-dimethyl-2,16-bis(1-methylpiperidin-1-ium-1-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate; [(2S,3S,5S,8R,9S,10S,13S,14S,16S,17R)-17-acetyloxy-10,13-dimethyl-2,16-bis(1-methylpiperidin-1-ium-1-yl)-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate dibromide; 1,1'-(3,17-Bis(acetyloxy)androstane-2,16-diyl)bis(1-methylpiperidinium) dibromide; 1,1'-(3alpha,17beta-Bis(acetyloxy)-5alpha-androstane-2beta,16beta-diyl)bis(1-methylpiperidinium) dibromide; 1,1'-(3alpha,17beta-Dihydroxy-5alpha-androstan-2beta,16beta-ylene)bis(1-methylpiperidinium) dibromide diacetate; 1,1'-([2beta,3alpha,5alpha,16beta,17beta]-3,17-Bis[acetyloxy]androstane-2,16-diyl)bis(1-methylpiperidinium) dibromide; 1,1'-[(2beta,3alpha,5alpha,16beta,17beta)-3,17-bis(Acetyloxy)androstane-2,16-diyl]bis(1-methylpiperidinium) dibromide; 2beta,16beta-Dipiperidino-5alpha-androstane-3alpha,17beta-diol diacetate dimethobromide; 2beta,16beta-Dipiperidino-5alpha-androstane-3alpha,17beta-dioldiacetatedimethobromide; 3-alpha,17-beta-Diacetoxy-2-beta,16-beta-dipiperidino-5-alpha-androstane dimethobromide; 3alpha,17beta-Diacetoxy-2beta,16beta-dipiperidino-5alpha-androstane dimethobromide; 3alpha,17beta-diacetoxy-2beta,16beta-bis(1-methylpiperidinium-1-yl)-5alpha-androstane; 3alpha,17beta-diacetoxy-2beta,16beta-bis(1-methylpiperidinium-1-yl)-5alpha-androstane dibromide; 5alpha-Androstan-3alpha,17beta-diol, 2beta,16beta-dipipecolinio-, dibromide, diacetate
Therapeutic ClassNeuromuscular Nondepolarizing Agents
Cross-matching ID
PubChem CID
441289
ChEBI ID
CHEMBL7907
CAS Number
CAS 16974-53-1
TTD Drug ID
D0AA0L
VARIDT Drug ID
DR00589

Consensus Signature of Drug Pharmacogenomic Perturbation (DPP)

Term Name NES FDR q-val Tag % Leading Edge Genes
Relaxin signaling pathway -1.67 3.11e-2 114/129 (88.37%) CREB5;PLCB3;GNAI1;...
Collecting duct acid secretion -1.69 2.97e-2 22/27 (81.48%) ATP6V0C;ATP6V1G1;ATP6V1E1;...
Epithelial cell signaling in Helicobacter pylori infect... -1.69 3.07e-2 62/70 (88.57%) ATP6V0C;SRC;ATP6V1G1;...
Gastric acid secretion -1.69 3.19e-2 63/76 (82.89%) PLCB3;GNAI1;SLC9A1;...
Coronavirus disease -1.70 3.03e-2 215/232 (92.67%) RPL14;EGFR;CASP1;...
Non-small cell lung cancer -1.71 2.97e-2 70/72 (97.22%) EGFR;RAF1;HGF;...
Complement and coagulation cascades -1.72 2.91e-2 76/85 (89.41%) F13A1;ITGAM;CFI;...
Salivary secretion -1.73 2.90e-2 76/93 (81.72%) PLCB3;SLC9A1;ATP1B1;...
Morphine addiction -1.74 2.70e-2 80/91 (87.91%) GABBR1;PDE8B;GABRG2;...
Mitophagy -1.75 2.33e-2 56/68 (82.35%) TBC1D15;RRAS;PINK1;...
Lysosome -1.77 1.78e-2 115/128 (89.84%) ACP2;ARSB;ENTPD4;...
Platelet activation -1.77 1.80e-2 106/124 (85.48%) PLCB3;GNAI1;MYL12B;...
Alanine, aspartate and glutamate metabolism -1.78 1.90e-2 27/37 (72.97%) GAD2;GFPT1;ASRGL1;...
T cell receptor signaling pathway -1.79 1.83e-2 93/104 (89.42%) IL10;IFNG;PAK2;...
Ferroptosis -1.79 1.86e-2 36/41 (87.8%) GPX4;ACSL6;MAP1LC3C;...
Leishmaniasis -1.80 1.98e-2 67/77 (87.01%) ITGAM;FCGR3B;NFKBIA;...
Natural killer cell mediated cytotoxicity -1.80 2.12e-2 99/131 (75.57%) PIK3CA;IFNA14;KLRK1;...
NOD-like receptor signaling pathway -1.80 2.17e-2 145/181 (80.11%) PLCB3;ATG12;DNM1L;...
Primary immunodeficiency -1.81 2.35e-2 33/38 (86.84%) CD40LG;PTPRC;ADA;...
Yersinia infection -1.84 1.75e-2 120/137 (87.59%) PIP5K1B;IRAK4;ARPC1A;...
Cholinergic synapse -1.85 1.93e-2 99/113 (87.61%) CREB5;PLCB3;GNAI1;...
Vibrio cholerae infection -1.88 1.15e-2 44/50 (88%) ATP6V0C;ARF1;KDELR1;...
Thiamine metabolism -1.90 1.11e-2 12/15 (80%) AK1;TPK1;ALPG;...
Human immunodeficiency virus 1 infection -1.91 1.06e-2 189/212 (89.15%) CD3G;FBXW11;HLA-B;...
B cell receptor signaling pathway -1.99 4.95e-3 71/81 (87.65%) LILRA5;LILRB1;LILRB4;...
Phagosome -2.01 5.94e-3 118/152 (77.63%) ATP6V1G1;COLEC11;ATP6V1E1;...
GABAergic synapse -2.01 7.42e-3 76/89 (85.39%) SLC6A13;ADCY7;SRC;...
PD-L1 expression and PD-1 checkpoint pathway in cancer -2.08 0.00e+0 79/89 (88.76%) IFNGR2;IFNG;HIF1A;...
Osteoclast differentiation -2.19 0.00e+0 117/127 (92.13%) IFNGR2;SIRPB1;IFNG;...
Neutrophil extracellular trap formation -2.28 0.00e+0 101/189 (53.44%) TLR7;ITGB3;CAMP;...
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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 6.66uM 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