(1R,2S,8S)-2-hydroxy-2-methyl-1,3,5,6,7,8-hexahydropyrrolizine-1-carboxylic acid

Details

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Internal ID d09af189-daef-43e7-83f0-02505562328d
Taxonomy Organoheterocyclic compounds > Pyrrolizidines
IUPAC Name (1R,2S,8S)-2-hydroxy-2-methyl-1,3,5,6,7,8-hexahydropyrrolizine-1-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H15NO3/c1-9(13)5-10-4-2-3-6(10)7(9)8(11)12/h6-7,13H,2-5H2,1H3,(H,11,12)/t6-,7-,9+/m0/s1
InChI Key NXSSHBBKWONHSM-ACLDMZEESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C9H15NO3
Molecular Weight 185.22 g/mol
Exact Mass 185.10519334 g/mol
Topological Polar Surface Area (TPSA) 60.80 Ų
XlogP -2.00
Atomic LogP (AlogP) -0.08
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2S,8S)-2-hydroxy-2-methyl-1,3,5,6,7,8-hexahydropyrrolizine-1-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8265 82.65%
Caco-2 + 0.7397 73.97%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.5843 58.43%
OATP2B1 inhibitior - 0.8428 84.28%
OATP1B1 inhibitior + 0.9446 94.46%
OATP1B3 inhibitior + 0.9512 95.12%
MATE1 inhibitior - 0.9609 96.09%
OCT2 inhibitior - 0.6500 65.00%
BSEP inhibitior - 0.9163 91.63%
P-glycoprotein inhibitior - 0.9748 97.48%
P-glycoprotein substrate - 0.9259 92.59%
CYP3A4 substrate - 0.5494 54.94%
CYP2C9 substrate - 0.6219 62.19%
CYP2D6 substrate - 0.6634 66.34%
CYP3A4 inhibition - 0.9631 96.31%
CYP2C9 inhibition - 0.9143 91.43%
CYP2C19 inhibition - 0.8814 88.14%
CYP2D6 inhibition - 0.9022 90.22%
CYP1A2 inhibition - 0.8610 86.10%
CYP2C8 inhibition - 0.9695 96.95%
CYP inhibitory promiscuity - 0.9768 97.68%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.4798 47.98%
Eye corrosion - 0.9801 98.01%
Eye irritation - 0.6723 67.23%
Skin irritation - 0.7154 71.54%
Skin corrosion - 0.8687 86.87%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6857 68.57%
Micronuclear - 0.5900 59.00%
Hepatotoxicity + 0.7691 76.91%
skin sensitisation - 0.8549 85.49%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.8500 85.00%
Nephrotoxicity + 0.5686 56.86%
Acute Oral Toxicity (c) III 0.6074 60.74%
Estrogen receptor binding - 0.8337 83.37%
Androgen receptor binding - 0.6468 64.68%
Thyroid receptor binding - 0.8253 82.53%
Glucocorticoid receptor binding - 0.8421 84.21%
Aromatase binding - 0.8163 81.63%
PPAR gamma - 0.7777 77.77%
Honey bee toxicity - 0.9843 98.43%
Biodegradation - 0.5500 55.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.8396 83.96%

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 91.41% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.15% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.46% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.04% 97.25%
CHEMBL4040 P28482 MAP kinase ERK2 85.92% 83.82%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.42% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.21% 95.89%
CHEMBL284 P27487 Dipeptidyl peptidase IV 82.26% 95.69%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 81.19% 93.04%
CHEMBL340 P08684 Cytochrome P450 3A4 80.98% 91.19%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.78% 93.00%

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.
Arnica lanceolata subsp. prima

Cross-Links

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PubChem 131141634
LOTUS LTS0018628
wikiData Q105187310