(S)-Tamsulosin Hydrochloride

Details

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Internal ID c6987431-77ea-4525-9664-51147604946b
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenethylamines > Amphetamines and derivatives
IUPAC Name 5-[(2S)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-2-methoxybenzenesulfonamide;hydrochloride
SMILES (Canonical) CCOC1=CC=CC=C1OCCNC(C)CC2=CC(=C(C=C2)OC)S(=O)(=O)N.Cl
SMILES (Isomeric) CCOC1=CC=CC=C1OCCN[C@@H](C)CC2=CC(=C(C=C2)OC)S(=O)(=O)N.Cl
InChI InChI=1S/C20H28N2O5S.ClH/c1-4-26-17-7-5-6-8-18(17)27-12-11-22-15(2)13-16-9-10-19(25-3)20(14-16)28(21,23)24;/h5-10,14-15,22H,4,11-13H2,1-3H3,(H2,21,23,24);1H/t15-;/m0./s1
InChI Key ZZIZZTHXZRDOFM-RSAXXLAASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H29ClN2O5S
Molecular Weight 445.00 g/mol
Exact Mass 444.1485709 g/mol
Topological Polar Surface Area (TPSA) 108.00 Ų
XlogP 0.00
Atomic LogP (AlogP) 2.76
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 11

Synonyms

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106463-19-8
5-[(2S)-2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-2-methoxybenzenesulfonamide;hydrochloride
ent-tamsulosin hydrochloride
(+)-LY 253352
SCHEMBL9300408
DTXSID00275650
CHEBI:142550
5-[(2S)-2-[[2-(-Ethoxyphenoxy)ethyl]amino]propyl]-2-methoxybenzenesulfonamide Hydrochloride
J-001597
(+)-(S)-5-(2-((2-(o-ethoxyphenoxy)ethyl)amino)propyl)-2-methoxybenzenesulfonamide monohydrochloride
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (S)-Tamsulosin Hydrochloride

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9967 99.67%
Caco-2 - 0.6310 63.10%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.9286 92.86%
Subcellular localzation Mitochondria 0.4297 42.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9500 95.00%
OATP1B3 inhibitior + 0.9400 94.00%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.6122 61.22%
P-glycoprotein inhibitior + 0.6764 67.64%
P-glycoprotein substrate + 0.5837 58.37%
CYP3A4 substrate + 0.5806 58.06%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4570 45.70%
CYP3A4 inhibition + 0.7645 76.45%
CYP2C9 inhibition + 0.5766 57.66%
CYP2C19 inhibition + 0.5521 55.21%
CYP2D6 inhibition - 0.8160 81.60%
CYP1A2 inhibition - 0.7273 72.73%
CYP2C8 inhibition + 0.5313 53.13%
CYP inhibitory promiscuity + 0.5153 51.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5704 57.04%
Carcinogenicity (trinary) Non-required 0.5805 58.05%
Eye corrosion - 0.9854 98.54%
Eye irritation - 0.9870 98.70%
Skin irritation - 0.7690 76.90%
Skin corrosion - 0.9206 92.06%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7260 72.60%
Micronuclear + 0.8300 83.00%
Hepatotoxicity + 0.7908 79.08%
skin sensitisation - 0.8414 84.14%
Respiratory toxicity + 0.9222 92.22%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity - 0.8429 84.29%
Acute Oral Toxicity (c) III 0.5369 53.69%
Estrogen receptor binding + 0.5366 53.66%
Androgen receptor binding + 0.8696 86.96%
Thyroid receptor binding - 0.8319 83.19%
Glucocorticoid receptor binding + 0.8970 89.70%
Aromatase binding - 0.5860 58.60%
PPAR gamma + 0.6154 61.54%
Honey bee toxicity - 0.6783 67.83%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9878 98.78%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL205 P00918 Carbonic anhydrase II 99.15% 98.44%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.70% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.06% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 94.12% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.73% 95.56%
CHEMBL2535 P11166 Glucose transporter 92.19% 98.75%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.06% 94.00%
CHEMBL3594 Q16790 Carbonic anhydrase IX 91.73% 99.23%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.09% 85.14%
CHEMBL1255126 O15151 Protein Mdm4 90.72% 90.20%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 89.05% 97.21%
CHEMBL3401 O75469 Pregnane X receptor 87.15% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.07% 99.17%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 85.48% 95.83%
CHEMBL261 P00915 Carbonic anhydrase I 84.83% 96.76%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.04% 97.14%
CHEMBL3729 P22748 Carbonic anhydrase IV 82.45% 99.23%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.51% 90.24%
CHEMBL2321614 Q9NPC2 Potassium channel subfamily K member 9 81.49% 80.00%
CHEMBL2319 P06870 Kallikrein 1 81.40% 90.95%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 81.26% 96.95%
CHEMBL1287628 Q9Y5S8 NADPH oxidase 1 80.62% 95.48%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.23% 96.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.20% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Asarum heterotropoides
Asarum sieboldii

Cross-Links

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PubChem 60146
NPASS NPC74295