(7aS)-2,3,5,7a-Tetrahydro-1H-pyrrolizine-7-methanol

Details

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Internal ID fd257d9d-9c2b-4155-a1cb-edc1fcf38a5a
Taxonomy Alkaloids and derivatives
IUPAC Name [(8S)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methanol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H13NO/c10-6-7-3-5-9-4-1-2-8(7)9/h3,8,10H,1-2,4-6H2/t8-/m0/s1
InChI Key XMJAZPFSQQKHEG-QMMMGPOBSA-N
Popularity 7 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 -0.30
Atomic LogP (AlogP) 0.38
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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551-59-7
AC1L4V7M
AC1Q77PJ
AR-1C3934
1h-pyrrolizine-7-methanol, 2,3,5,7a-tetrahydro-,(s)-
CHEBI:9360
SCHEMBL19317459
DTXSID101221884
Q27108359
(7aS)-2,3,5,7a-Tetrahydro-1H-pyrrolizine-7-methanol
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (7aS)-2,3,5,7a-Tetrahydro-1H-pyrrolizine-7-methanol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9802 98.02%
Caco-2 + 0.7435 74.35%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4896 48.96%
OATP2B1 inhibitior - 0.8451 84.51%
OATP1B1 inhibitior + 0.9506 95.06%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior - 0.8960 89.60%
P-glycoprotein inhibitior - 0.9906 99.06%
P-glycoprotein substrate - 0.8998 89.98%
CYP3A4 substrate - 0.6842 68.42%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate + 0.6449 64.49%
CYP3A4 inhibition - 0.9931 99.31%
CYP2C9 inhibition - 0.8878 88.78%
CYP2C19 inhibition - 0.8673 86.73%
CYP2D6 inhibition - 0.8773 87.73%
CYP1A2 inhibition - 0.6090 60.90%
CYP2C8 inhibition - 0.9771 97.71%
CYP inhibitory promiscuity - 0.9257 92.57%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.5023 50.23%
Eye corrosion - 0.7692 76.92%
Eye irritation + 0.8983 89.83%
Skin irritation - 0.5115 51.15%
Skin corrosion - 0.5081 50.81%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6660 66.60%
Micronuclear - 0.6300 63.00%
Hepatotoxicity + 0.8407 84.07%
skin sensitisation - 0.8052 80.52%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5125 51.25%
Acute Oral Toxicity (c) III 0.5366 53.66%
Estrogen receptor binding - 0.9613 96.13%
Androgen receptor binding - 0.8020 80.20%
Thyroid receptor binding - 0.9243 92.43%
Glucocorticoid receptor binding - 0.8023 80.23%
Aromatase binding - 0.8504 85.04%
PPAR gamma - 0.8644 86.44%
Honey bee toxicity - 0.9720 97.20%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.8088 80.88%

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 91.30% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.03% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.03% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.01% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.05% 95.89%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.64% 91.11%

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.
Heliotropium curassavicum
Heliotropium indicum

Cross-Links

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PubChem 164663
LOTUS LTS0156424
wikiData Q27108359