Atidine

Details

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Internal ID 6c795652-942c-40db-997d-9d5d61badd0e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Villanovane, atisane, trachylobane or helvifulvane diterpenoids > Atisane diterpenoids
IUPAC Name (1S,2S,4S,6R,7S,10R,11R)-6-hydroxy-13-(2-hydroxyethyl)-11-methyl-5-methylidene-13-azapentacyclo[9.3.3.24,7.01,10.02,7]nonadecan-8-one
SMILES (Canonical) CC12CCCC3(C1CC(=O)C45C3CC(CC4)C(=C)C5O)CN(C2)CCO
SMILES (Isomeric) C[C@@]12CCC[C@@]3([C@@H]1CC(=O)[C@]45[C@H]3C[C@H](CC4)C(=C)[C@H]5O)CN(C2)CCO
InChI InChI=1S/C22H33NO3/c1-14-15-4-7-22(19(14)26)17(10-15)21-6-3-5-20(2,16(21)11-18(22)25)12-23(13-21)8-9-24/h15-17,19,24,26H,1,3-13H2,2H3/t15-,16+,17-,19+,20-,21-,22+/m0/s1
InChI Key LDYSWDMNYLEUCU-CCXLZGIPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H33NO3
Molecular Weight 359.50 g/mol
Exact Mass 359.24604391 g/mol
Topological Polar Surface Area (TPSA) 60.80 Ų
XlogP 1.60
Atomic LogP (AlogP) 2.39
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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CHEMBL4065019
467-91-4
DTXSID101019908
BDBM50242320

2D Structure

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2D Structure of Atidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9644 96.44%
Caco-2 + 0.5757 57.57%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.4755 47.55%
OATP2B1 inhibitior - 0.8609 86.09%
OATP1B1 inhibitior + 0.8980 89.80%
OATP1B3 inhibitior + 0.9466 94.66%
MATE1 inhibitior - 0.9646 96.46%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.4641 46.41%
P-glycoprotein inhibitior - 0.8014 80.14%
P-glycoprotein substrate - 0.5518 55.18%
CYP3A4 substrate + 0.6530 65.30%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate + 0.3504 35.04%
CYP3A4 inhibition - 0.7594 75.94%
CYP2C9 inhibition - 0.8586 85.86%
CYP2C19 inhibition - 0.8601 86.01%
CYP2D6 inhibition - 0.8349 83.49%
CYP1A2 inhibition - 0.8576 85.76%
CYP2C8 inhibition - 0.7529 75.29%
CYP inhibitory promiscuity - 0.9534 95.34%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5465 54.65%
Eye corrosion - 0.9819 98.19%
Eye irritation - 0.8813 88.13%
Skin irritation - 0.6972 69.72%
Skin corrosion - 0.8797 87.97%
Ames mutagenesis - 0.7154 71.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7595 75.95%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.5098 50.98%
skin sensitisation - 0.8115 81.15%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.7291 72.91%
Acute Oral Toxicity (c) III 0.6300 63.00%
Estrogen receptor binding + 0.8040 80.40%
Androgen receptor binding + 0.6617 66.17%
Thyroid receptor binding + 0.6945 69.45%
Glucocorticoid receptor binding + 0.7480 74.80%
Aromatase binding + 0.6521 65.21%
PPAR gamma - 0.4936 49.36%
Honey bee toxicity - 0.8688 86.88%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.6501 65.01%

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
CHEMBL4040 P28482 MAP kinase ERK2 99.91% 83.82%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.84% 97.25%
CHEMBL2581 P07339 Cathepsin D 96.42% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.82% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 94.28% 94.75%
CHEMBL2140 P48775 Tryptophan 2,3-dioxygenase 93.53% 98.46%
CHEMBL3192 Q9BY41 Histone deacetylase 8 91.06% 93.99%
CHEMBL228 P31645 Serotonin transporter 90.55% 95.51%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 89.17% 96.38%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 88.34% 82.69%
CHEMBL226 P30542 Adenosine A1 receptor 87.82% 95.93%
CHEMBL238 Q01959 Dopamine transporter 87.66% 95.88%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.20% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.42% 95.56%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 84.86% 93.03%
CHEMBL1902 P62942 FK506-binding protein 1A 84.64% 97.05%
CHEMBL5103 Q969S8 Histone deacetylase 10 84.60% 90.08%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.26% 90.71%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 83.76% 95.83%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.33% 86.33%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 83.18% 91.07%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.16% 100.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.88% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.01% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.80% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.25% 93.04%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.00% 99.23%

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.
Aconitum heterophyllum
Aconitum seravschanicum

Cross-Links

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PubChem 12299861
LOTUS LTS0234621
wikiData Q104402366