Dihydrocuscohygrine

Details

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Internal ID d6955a34-30cf-4887-9ed7-710487483738
Taxonomy Organoheterocyclic compounds > Pyrrolidines > N-alkylpyrrolidines
IUPAC Name 1,3-bis[(2S)-1-methylpyrrolidin-2-yl]propan-2-ol
SMILES (Canonical) CN1CCCC1CC(CC2CCCN2C)O
SMILES (Isomeric) CN1CCC[C@H]1CC(C[C@@H]2CCCN2C)O
InChI InChI=1S/C13H26N2O/c1-14-7-3-5-11(14)9-13(16)10-12-6-4-8-15(12)2/h11-13,16H,3-10H2,1-2H3/t11-,12-/m0/s1
InChI Key UOJNOOLFFFFKNA-RYUDHWBXSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C13H26N2O
Molecular Weight 226.36 g/mol
Exact Mass 226.204513457 g/mol
Topological Polar Surface Area (TPSA) 26.70 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.32
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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Dihydrocuscohygrine, (-)-
S8NA96NN7T
58131-40-1
DTXSID901045577
1,3-bis[(2S)-1-methylpyrrolidin-2-yl]propan-2-ol
1,3-bis((2S)-1-methylpyrrolidin-2-yl)propan-2-ol
RefChem:133779
DTXCID401527502
Cuscohygrinol
(-)-Dihydrocuscohygrine
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Dihydrocuscohygrine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8928 89.28%
Caco-2 + 0.7459 74.59%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Lysosomes 0.5354 53.54%
OATP2B1 inhibitior - 0.8496 84.96%
OATP1B1 inhibitior + 0.9631 96.31%
OATP1B3 inhibitior + 0.9414 94.14%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.5750 57.50%
BSEP inhibitior - 0.8681 86.81%
P-glycoprotein inhibitior - 0.9489 94.89%
P-glycoprotein substrate - 0.8172 81.72%
CYP3A4 substrate - 0.6619 66.19%
CYP2C9 substrate - 0.6220 62.20%
CYP2D6 substrate + 0.6700 67.00%
CYP3A4 inhibition - 0.9863 98.63%
CYP2C9 inhibition - 0.9634 96.34%
CYP2C19 inhibition - 0.9070 90.70%
CYP2D6 inhibition - 0.8883 88.83%
CYP1A2 inhibition - 0.9377 93.77%
CYP2C8 inhibition - 0.9955 99.55%
CYP inhibitory promiscuity - 0.9949 99.49%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5996 59.96%
Eye corrosion - 0.8165 81.65%
Eye irritation + 0.7971 79.71%
Skin irritation - 0.6206 62.06%
Skin corrosion + 0.6594 65.94%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6157 61.57%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5374 53.74%
skin sensitisation - 0.8839 88.39%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6869 68.69%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.8499 84.99%
Acute Oral Toxicity (c) III 0.6829 68.29%
Estrogen receptor binding - 0.7490 74.90%
Androgen receptor binding - 0.7985 79.85%
Thyroid receptor binding - 0.6767 67.67%
Glucocorticoid receptor binding - 0.8109 81.09%
Aromatase binding - 0.7997 79.97%
PPAR gamma - 0.8225 82.25%
Honey bee toxicity - 0.9490 94.90%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.8976 89.76%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.48% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.26% 97.25%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.78% 85.14%
CHEMBL2581 P07339 Cathepsin D 92.93% 98.95%
CHEMBL5203 P33316 dUTP pyrophosphatase 92.10% 99.18%
CHEMBL238 Q01959 Dopamine transporter 86.89% 95.88%
CHEMBL4072 P07858 Cathepsin B 85.71% 93.67%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 85.68% 95.58%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 84.29% 98.33%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 84.24% 98.46%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.60% 95.89%
CHEMBL240 Q12809 HERG 83.07% 89.76%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.97% 97.09%
CHEMBL2730 P21980 Protein-glutamine gamma-glutamyltransferase 80.57% 92.38%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 80.32% 96.03%

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.
Erythroxylum cataractarum
Erythroxylum monogynum

Cross-Links

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PubChem 11075129
LOTUS LTS0007911
wikiData Q15634215