Sedridine

Details

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Internal ID dd4834db-858c-4da5-84da-6e7e153e6551
Taxonomy Organoheterocyclic compounds > Piperidines
IUPAC Name (2S)-1-[(2S)-piperidin-2-yl]propan-2-ol
SMILES (Canonical) CC(CC1CCCCN1)O
SMILES (Isomeric) C[C@@H](C[C@@H]1CCCCN1)O
InChI InChI=1S/C8H17NO/c1-7(10)6-8-4-2-3-5-9-8/h7-10H,2-6H2,1H3/t7-,8-/m0/s1
InChI Key GFKFBLJVPWRDEL-YUMQZZPRSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C8H17NO
Molecular Weight 143.23 g/mol
Exact Mass 143.131014166 g/mol
Topological Polar Surface Area (TPSA) 32.30 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.90
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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(2s)-1-[(2s)-piperidin-2-yl]propan-2-ol
501-83-7
DTXSID90198208
(S-(R*,R*))-alpha-Methyl-2-piperidineethanol

2D Structure

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2D Structure of Sedridine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9460 94.60%
Caco-2 + 0.7346 73.46%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6382 63.82%
OATP2B1 inhibitior - 0.8425 84.25%
OATP1B1 inhibitior + 0.9676 96.76%
OATP1B3 inhibitior + 0.9479 94.79%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.9496 94.96%
P-glycoprotein inhibitior - 0.9793 97.93%
P-glycoprotein substrate - 0.8586 85.86%
CYP3A4 substrate - 0.6994 69.94%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.5555 55.55%
CYP3A4 inhibition - 0.9838 98.38%
CYP2C9 inhibition - 0.9308 93.08%
CYP2C19 inhibition - 0.9574 95.74%
CYP2D6 inhibition - 0.7017 70.17%
CYP1A2 inhibition - 0.8611 86.11%
CYP2C8 inhibition - 0.9766 97.66%
CYP inhibitory promiscuity - 0.9770 97.70%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7013 70.13%
Eye corrosion + 0.6082 60.82%
Eye irritation + 0.8581 85.81%
Skin irritation - 0.5201 52.01%
Skin corrosion + 0.5279 52.79%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7557 75.57%
Micronuclear - 0.7800 78.00%
Hepatotoxicity + 0.6784 67.84%
skin sensitisation - 0.7757 77.57%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.7197 71.97%
Acute Oral Toxicity (c) III 0.6824 68.24%
Estrogen receptor binding - 0.8841 88.41%
Androgen receptor binding - 0.7848 78.48%
Thyroid receptor binding - 0.7998 79.98%
Glucocorticoid receptor binding - 0.8108 81.08%
Aromatase binding - 0.8597 85.97%
PPAR gamma - 0.8737 87.37%
Honey bee toxicity - 0.9816 98.16%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.8300 83.00%
Fish aquatic toxicity - 0.9698 96.98%

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 95.75% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.51% 97.25%
CHEMBL2581 P07339 Cathepsin D 93.96% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.92% 97.09%
CHEMBL213 P08588 Beta-1 adrenergic receptor 89.61% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.29% 94.45%
CHEMBL237 P41145 Kappa opioid receptor 87.51% 98.10%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 87.19% 93.03%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.68% 92.88%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 84.29% 96.47%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.27% 85.14%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.98% 93.56%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.41% 96.95%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 82.33% 95.58%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 80.35% 97.21%

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.
Picea breweriana
Sedum anglicum
Sedum litoreum

Cross-Links

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PubChem 164633
LOTUS LTS0039741
wikiData Q83070991