(1r,2s)-n-Methylephedrine

Details

Top
Internal ID 8ea39cf0-b11b-45a8-b9c7-1978dcce21ef
Taxonomy Benzenoids > Benzene and substituted derivatives > Phenylpropanes
IUPAC Name [(1R,2S)-1-hydroxy-1-phenylpropan-2-yl]-dimethylazanium
SMILES (Canonical) CC(C(C1=CC=CC=C1)O)[NH+](C)C
SMILES (Isomeric) C[C@@H]([C@@H](C1=CC=CC=C1)O)[NH+](C)C
InChI InChI=1S/C11H17NO/c1-9(12(2)3)11(13)10-7-5-4-6-8-10/h4-9,11,13H,1-3H3/p+1/t9-,11-/m0/s1
InChI Key FMCGSUUBYTWNDP-ONGXEEELSA-O
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C11H18NO+
Molecular Weight 180.27 g/mol
Exact Mass 180.138839198 g/mol
Topological Polar Surface Area (TPSA) 24.70 Ų
XlogP 1.70
Atomic LogP (AlogP) 0.25
H-Bond Acceptor 1
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

Top
Erythro-alpha-[1-(dimethylamino)ethyl]benzyl alcohol
(1r,2s)-n-methylephedrine

2D Structure

Top
2D Structure of (1r,2s)-n-Methylephedrine

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6870 68.70%
Caco-2 + 0.9366 93.66%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.5601 56.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9482 94.82%
OATP1B3 inhibitior + 0.9509 95.09%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8758 87.58%
P-glycoprotein inhibitior - 0.9754 97.54%
P-glycoprotein substrate - 0.9567 95.67%
CYP3A4 substrate - 0.7687 76.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.4605 46.05%
CYP3A4 inhibition - 0.9163 91.63%
CYP2C9 inhibition - 0.8578 85.78%
CYP2C19 inhibition - 0.8143 81.43%
CYP2D6 inhibition - 0.6627 66.27%
CYP1A2 inhibition - 0.7257 72.57%
CYP2C8 inhibition - 0.9887 98.87%
CYP inhibitory promiscuity - 0.9125 91.25%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6820 68.20%
Carcinogenicity (trinary) Non-required 0.6345 63.45%
Eye corrosion - 0.9624 96.24%
Eye irritation - 0.8896 88.96%
Skin irritation - 0.6530 65.30%
Skin corrosion - 0.5406 54.06%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6382 63.82%
Micronuclear + 0.6300 63.00%
Hepatotoxicity + 0.5710 57.10%
skin sensitisation - 0.8362 83.62%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity - 0.5111 51.11%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7225 72.25%
Acute Oral Toxicity (c) III 0.6622 66.22%
Estrogen receptor binding - 0.8749 87.49%
Androgen receptor binding - 0.6357 63.57%
Thyroid receptor binding - 0.8305 83.05%
Glucocorticoid receptor binding - 0.9144 91.44%
Aromatase binding - 0.9001 90.01%
PPAR gamma - 0.8714 87.14%
Honey bee toxicity - 0.9541 95.41%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity - 0.7587 75.87%

Targets

Top

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
CHEMBL2581 P07339 Cathepsin D 94.15% 98.95%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 89.16% 94.08%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.92% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.70% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 87.61% 90.17%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 86.13% 94.62%
CHEMBL3902 P09211 Glutathione S-transferase Pi 85.84% 93.81%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.84% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 80.11% 94.73%

Plants that contains it

Top
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.
Ephedra equisetina
Ephedra intermedia
Ephedra sinica

Cross-Links

Top
PubChem 6918907
NPASS NPC214201