Myosmine

Details

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Internal ID 2dd73397-4ef9-46be-bfdb-2f9f017b5cb7
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives
IUPAC Name 3-(3,4-dihydro-2H-pyrrol-5-yl)pyridine
SMILES (Canonical) C1CC(=NC1)C2=CN=CC=C2
SMILES (Isomeric) C1CC(=NC1)C2=CN=CC=C2
InChI InChI=1S/C9H10N2/c1-3-8(7-10-5-1)9-4-2-6-11-9/h1,3,5,7H,2,4,6H2
InChI Key DPNGWXJMIILTBS-UHFFFAOYSA-N
Popularity 239 references in papers

Physical and Chemical Properties

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Molecular Formula C9H10N2
Molecular Weight 146.19 g/mol
Exact Mass 146.084398327 g/mol
Topological Polar Surface Area (TPSA) 25.20 Ų
XlogP 0.60
Atomic LogP (AlogP) 1.66
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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532-12-7
3-(3,4-Dihydro-2H-pyrrol-5-yl)pyridine
3-(1-Pyrrolin-2-yl)pyridine
Miosmine
Pyridine, 3-(3,4-dihydro-2H-pyrrol-5-yl)-
3-(4,5-Dihydro-3H-pyrrol-2-yl)-pyridine
2-(3-Pyridyl)-1-pyrroline
3-(1-PYRROLIN-2-YL)-PYRIDINE
MFCD00052019
CHEBI:7051
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Myosmine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9886 98.86%
Caco-2 + 0.9553 95.53%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.8000 80.00%
Subcellular localzation Mitochondria 0.7158 71.58%
OATP2B1 inhibitior - 0.8720 87.20%
OATP1B1 inhibitior + 0.9745 97.45%
OATP1B3 inhibitior + 0.9495 94.95%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior - 0.8918 89.18%
P-glycoprotein inhibitior - 0.9949 99.49%
P-glycoprotein substrate - 0.9381 93.81%
CYP3A4 substrate - 0.7062 70.62%
CYP2C9 substrate - 0.6198 61.98%
CYP2D6 substrate - 0.7828 78.28%
CYP3A4 inhibition - 0.8309 83.09%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9025 90.25%
CYP2D6 inhibition - 0.9231 92.31%
CYP1A2 inhibition + 0.9106 91.06%
CYP2C8 inhibition - 0.6583 65.83%
CYP inhibitory promiscuity - 0.6210 62.10%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6730 67.30%
Eye corrosion - 0.8222 82.22%
Eye irritation + 0.9617 96.17%
Skin irritation + 0.6085 60.85%
Skin corrosion + 0.6184 61.84%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4803 48.03%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8029 80.29%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.7085 70.85%
Acute Oral Toxicity (c) III 0.8037 80.37%
Estrogen receptor binding - 0.6720 67.20%
Androgen receptor binding - 0.9503 95.03%
Thyroid receptor binding - 0.7137 71.37%
Glucocorticoid receptor binding - 0.6551 65.51%
Aromatase binding - 0.5104 51.04%
PPAR gamma - 0.4881 48.81%
Honey bee toxicity - 0.9169 91.69%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity - 0.7918 79.18%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1947 P10828 Thyroid hormone receptor beta-1 199.5 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 88.60% 98.95%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 86.96% 93.10%
CHEMBL1951 P21397 Monoamine oxidase A 86.55% 91.49%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.77% 96.09%
CHEMBL1907599 P05556 Integrin alpha-4/beta-1 84.64% 92.86%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.50% 86.33%
CHEMBL1075145 P55072 Transitional endoplasmic reticulum ATPase 83.78% 98.50%
CHEMBL3902 P09211 Glutathione S-transferase Pi 81.06% 93.81%
CHEMBL2378 P30307 Dual specificity phosphatase Cdc25C 80.14% 96.67%

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.
Duboisia hopwoodii
Nicotiana tabacum

Cross-Links

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PubChem 442649
LOTUS LTS0239576
wikiData Q411486