7-Methylidene-1,2,3,5,6,8-hexahydropyrrolizin-1-ol

Details

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Internal ID d764c7c3-f810-4db5-a1a9-ab634bd62e53
Taxonomy Organoheterocyclic compounds > Pyrrolizidines
IUPAC Name 7-methylidene-1,2,3,5,6,8-hexahydropyrrolizin-1-ol
SMILES (Canonical) C=C1CCN2C1C(CC2)O
SMILES (Isomeric) C=C1CCN2C1C(CC2)O
InChI InChI=1S/C8H13NO/c1-6-2-4-9-5-3-7(10)8(6)9/h7-8,10H,1-5H2
InChI Key OVTJHGIWYOOHFS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C8H13NO
Molecular Weight 139.19 g/mol
Exact Mass 139.099714038 g/mol
Topological Polar Surface Area (TPSA) 23.50 Ų
XlogP 0.10
Atomic LogP (AlogP) 0.38
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 7-Methylidene-1,2,3,5,6,8-hexahydropyrrolizin-1-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9912 99.12%
Caco-2 - 0.5439 54.39%
Blood Brain Barrier + 0.6879 68.79%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.5220 52.20%
OATP2B1 inhibitior - 0.8459 84.59%
OATP1B1 inhibitior + 0.9595 95.95%
OATP1B3 inhibitior + 0.9454 94.54%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior - 0.9299 92.99%
P-glycoprotein inhibitior - 0.9869 98.69%
P-glycoprotein substrate - 0.9342 93.42%
CYP3A4 substrate - 0.6166 61.66%
CYP2C9 substrate + 0.5852 58.52%
CYP2D6 substrate + 0.6289 62.89%
CYP3A4 inhibition - 0.9872 98.72%
CYP2C9 inhibition - 0.8925 89.25%
CYP2C19 inhibition - 0.8374 83.74%
CYP2D6 inhibition - 0.7555 75.55%
CYP1A2 inhibition - 0.7219 72.19%
CYP2C8 inhibition - 0.9778 97.78%
CYP inhibitory promiscuity - 0.9609 96.09%
UGT catelyzed + 1.0000 100.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4673 46.73%
Eye corrosion - 0.9185 91.85%
Eye irritation + 0.9624 96.24%
Skin irritation - 0.5938 59.38%
Skin corrosion - 0.6263 62.63%
Ames mutagenesis - 0.8200 82.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7226 72.26%
Micronuclear - 0.5200 52.00%
Hepatotoxicity + 0.8875 88.75%
skin sensitisation - 0.8277 82.77%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.5739 57.39%
Acute Oral Toxicity (c) III 0.5510 55.10%
Estrogen receptor binding - 0.9729 97.29%
Androgen receptor binding - 0.8501 85.01%
Thyroid receptor binding - 0.8835 88.35%
Glucocorticoid receptor binding - 0.7981 79.81%
Aromatase binding - 0.8950 89.50%
PPAR gamma - 0.8487 84.87%
Honey bee toxicity - 0.9064 90.64%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity - 0.8733 87.33%

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
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 84.77% 98.46%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.18% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.11% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.35% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.95% 92.94%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 80.52% 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.
Crotalaria goreensis
Senecio schweinfurthii

Cross-Links

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PubChem 5095795
LOTUS LTS0220315
wikiData Q105201410