Sclerolizine

Details

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Internal ID 4aa33856-bf3d-48ec-a8cd-1a9d5de548b3
Taxonomy Organoheterocyclic compounds > Pyrrolizines
IUPAC Name (8S)-2-hexadec-6-enoyl-1-hydroxy-5,6,7,8-tetrahydropyrrolizin-3-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H37NO3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-17-20(25)21-22(26)19-16-15-18-24(19)23(21)27/h10-11,19,26H,2-9,12-18H2,1H3/t19-/m0/s1
InChI Key VSRFLISPWPFUNO-IBGZPJMESA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H37NO3
Molecular Weight 375.50 g/mol
Exact Mass 375.27734404 g/mol
Topological Polar Surface Area (TPSA) 57.60 Ų
XlogP 6.60
Atomic LogP (AlogP) 5.63
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Sclerolizine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9903 99.03%
Caco-2 - 0.5289 52.89%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.6917 69.17%
OATP2B1 inhibitior - 0.8548 85.48%
OATP1B1 inhibitior + 0.7602 76.02%
OATP1B3 inhibitior + 0.9388 93.88%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6041 60.41%
BSEP inhibitior + 0.7641 76.41%
P-glycoprotein inhibitior - 0.5273 52.73%
P-glycoprotein substrate - 0.6502 65.02%
CYP3A4 substrate + 0.5424 54.24%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8888 88.88%
CYP3A4 inhibition - 0.9447 94.47%
CYP2C9 inhibition - 0.8424 84.24%
CYP2C19 inhibition - 0.8068 80.68%
CYP2D6 inhibition - 0.9223 92.23%
CYP1A2 inhibition - 0.6639 66.39%
CYP2C8 inhibition - 0.8533 85.33%
CYP inhibitory promiscuity - 0.8079 80.79%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5213 52.13%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.6914 69.14%
Skin irritation - 0.7587 75.87%
Skin corrosion - 0.9089 90.89%
Ames mutagenesis - 0.8969 89.69%
Human Ether-a-go-go-Related Gene inhibition - 0.5618 56.18%
Micronuclear - 0.5000 50.00%
Hepatotoxicity - 0.5674 56.74%
skin sensitisation - 0.8822 88.22%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6254 62.54%
Acute Oral Toxicity (c) III 0.6712 67.12%
Estrogen receptor binding + 0.5377 53.77%
Androgen receptor binding + 0.5613 56.13%
Thyroid receptor binding - 0.5627 56.27%
Glucocorticoid receptor binding - 0.4669 46.69%
Aromatase binding - 0.8336 83.36%
PPAR gamma + 0.6954 69.54%
Honey bee toxicity - 0.9767 97.67%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.8478 84.78%
Fish aquatic toxicity + 0.8385 83.85%

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
CHEMBL2581 P07339 Cathepsin D 99.21% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.90% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.17% 96.09%
CHEMBL1902 P62942 FK506-binding protein 1A 94.88% 97.05%
CHEMBL217 P14416 Dopamine D2 receptor 94.83% 95.62%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.17% 91.11%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 91.51% 100.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.95% 91.81%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.12% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.61% 95.56%
CHEMBL5255 O00206 Toll-like receptor 4 87.01% 92.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.92% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.79% 97.25%
CHEMBL2069156 Q14145 Kelch-like ECH-associated protein 1 85.55% 82.38%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 85.26% 96.00%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.14% 90.08%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.40% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 82.14% 89.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.02% 93.03%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.95% 94.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.92% 93.00%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 81.71% 97.50%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.52% 93.56%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.39% 90.24%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139585663
LOTUS LTS0122917
wikiData Q77484776