habbemines A

Details

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Internal ID a7f5ea55-df89-498c-af22-86f9dddcb244
Taxonomy Alkaloids and derivatives
IUPAC Name (5S,6S)-6-[2-[(2S)-1-(3-hydroxypropyl)pyrrolidin-2-yl]acetyl]-5-methylcyclohex-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H25NO3/c1-12-5-2-7-14(19)16(12)15(20)11-13-6-3-8-17(13)9-4-10-18/h2,7,12-13,16,18H,3-6,8-11H2,1H3/t12-,13-,16+/m0/s1
InChI Key RQOOACKVJJWLLA-HEHGZKQESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H25NO3
Molecular Weight 279.37 g/mol
Exact Mass 279.18344366 g/mol
Topological Polar Surface Area (TPSA) 57.60 Ų
XlogP 1.50
Atomic LogP (AlogP) 1.57
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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CHEMBL608816

2D Structure

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2D Structure of habbemines A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9920 99.20%
Caco-2 + 0.5711 57.11%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.6445 64.45%
OATP2B1 inhibitior - 0.8586 85.86%
OATP1B1 inhibitior + 0.8722 87.22%
OATP1B3 inhibitior + 0.9421 94.21%
MATE1 inhibitior - 0.9412 94.12%
OCT2 inhibitior + 0.5709 57.09%
BSEP inhibitior - 0.5517 55.17%
P-glycoprotein inhibitior - 0.8994 89.94%
P-glycoprotein substrate + 0.5102 51.02%
CYP3A4 substrate + 0.5718 57.18%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7972 79.72%
CYP3A4 inhibition - 0.8475 84.75%
CYP2C9 inhibition - 0.9312 93.12%
CYP2C19 inhibition - 0.9243 92.43%
CYP2D6 inhibition - 0.9260 92.60%
CYP1A2 inhibition - 0.8717 87.17%
CYP2C8 inhibition - 0.9039 90.39%
CYP inhibitory promiscuity - 0.9864 98.64%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.5494 54.94%
Eye corrosion - 0.9689 96.89%
Eye irritation - 0.9413 94.13%
Skin irritation - 0.6940 69.40%
Skin corrosion - 0.8581 85.81%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5695 56.95%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.6127 61.27%
skin sensitisation - 0.8831 88.31%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.7587 75.87%
Acute Oral Toxicity (c) III 0.6850 68.50%
Estrogen receptor binding - 0.7693 76.93%
Androgen receptor binding + 0.5753 57.53%
Thyroid receptor binding - 0.5870 58.70%
Glucocorticoid receptor binding + 0.6659 66.59%
Aromatase binding - 0.8357 83.57%
PPAR gamma - 0.7246 72.46%
Honey bee toxicity - 0.9605 96.05%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity - 0.6715 67.15%

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 97.13% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.64% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.50% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.68% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.01% 91.11%
CHEMBL217 P14416 Dopamine D2 receptor 86.38% 95.62%
CHEMBL226 P30542 Adenosine A1 receptor 85.42% 95.93%
CHEMBL4394 Q9NYA1 Sphingosine kinase 1 85.26% 96.03%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.19% 90.71%
CHEMBL4208 P20618 Proteasome component C5 84.42% 90.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.83% 93.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.95% 95.89%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 81.80% 98.46%
CHEMBL5103 Q969S8 Histone deacetylase 10 81.65% 90.08%
CHEMBL2916 O14746 Telomerase reverse transcriptase 81.58% 90.00%
CHEMBL2781 P19634 Sodium/hydrogen exchanger 1 80.95% 90.24%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 80.80% 86.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.78% 100.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.43% 91.07%

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.
Elaeocarpus habbemensis

Cross-Links

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PubChem 16747723
LOTUS LTS0030767
wikiData Q105243463