Hygrine

Details

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Internal ID 3db3c55e-b8de-4616-9954-fd28ce0c935a
Taxonomy Alkaloids and derivatives
IUPAC Name 1-[(2R)-1-methylpyrrolidin-2-yl]propan-2-one
SMILES (Canonical) CC(=O)CC1CCCN1C
SMILES (Isomeric) CC(=O)C[C@H]1CCCN1C
InChI InChI=1S/C8H15NO/c1-7(10)6-8-4-3-5-9(8)2/h8H,3-6H2,1-2H3/t8-/m1/s1
InChI Key ADKXZIOQKHHDNQ-MRVPVSSYSA-N
Popularity 215 references in papers

Physical and Chemical Properties

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Molecular Formula C8H15NO
Molecular Weight 141.21 g/mol
Exact Mass 141.115364102 g/mol
Topological Polar Surface Area (TPSA) 20.30 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.06
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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496-49-1
(+)-Hygrine
(R)-(+)-Hygrine
1-[(2R)-1-methylpyrrolidin-2-yl]propan-2-one
(+)-N-Methyl-2-acetonylpyrrolidine
(R)-hygrine
UNII-49H1LNM62X
49H1LNM62X
EINECS 207-822-0
1-(1-Methyl-2-pyrrolidinyl)-2-propanone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Hygrine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9650 96.50%
Caco-2 + 0.9177 91.77%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.4752 47.52%
OATP2B1 inhibitior - 0.8358 83.58%
OATP1B1 inhibitior + 0.9550 95.50%
OATP1B3 inhibitior + 0.9462 94.62%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior + 0.6500 65.00%
BSEP inhibitior - 0.9553 95.53%
P-glycoprotein inhibitior - 0.9792 97.92%
P-glycoprotein substrate - 0.7993 79.93%
CYP3A4 substrate - 0.6147 61.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5193 51.93%
CYP3A4 inhibition - 0.9821 98.21%
CYP2C9 inhibition - 0.9429 94.29%
CYP2C19 inhibition - 0.7827 78.27%
CYP2D6 inhibition - 0.8906 89.06%
CYP1A2 inhibition - 0.7599 75.99%
CYP2C8 inhibition - 0.9964 99.64%
CYP inhibitory promiscuity - 0.9808 98.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6873 68.73%
Eye corrosion - 0.8098 80.98%
Eye irritation + 0.9050 90.50%
Skin irritation - 0.5744 57.44%
Skin corrosion + 0.5800 58.00%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6180 61.80%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5587 55.87%
skin sensitisation - 0.8820 88.20%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.8100 81.00%
Acute Oral Toxicity (c) III 0.6288 62.88%
Estrogen receptor binding - 0.9358 93.58%
Androgen receptor binding - 0.8921 89.21%
Thyroid receptor binding - 0.9089 90.89%
Glucocorticoid receptor binding - 0.9083 90.83%
Aromatase binding - 0.8019 80.19%
PPAR gamma - 0.9360 93.60%
Honey bee toxicity - 0.9659 96.59%
Biodegradation + 0.8250 82.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity - 0.7974 79.74%

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 97.88% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.03% 97.25%
CHEMBL2581 P07339 Cathepsin D 91.07% 98.95%
CHEMBL5203 P33316 dUTP pyrophosphatase 85.76% 99.18%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.84% 85.14%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.02% 93.04%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 81.78% 95.50%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 81.76% 98.46%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.66% 95.56%
CHEMBL1795139 Q8IU80 Transmembrane protease serine 6 80.64% 98.33%

Cross-Links

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PubChem 440933
NPASS NPC35267
LOTUS LTS0186540
wikiData Q2376404