Inflexanin A

Details

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Internal ID 8b23f93c-6898-4122-be67-37f85d613c72
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Kaurane diterpenoids
IUPAC Name [(1S,3S,4S,6S,9R,10S,11S,13S)-3,11-dihydroxy-5,5,9-trimethyl-14-methylidene-15-oxo-6-tetracyclo[11.2.1.01,10.04,9]hexadecanyl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H32O5/c1-11-13-8-14(24)18-21(5)7-6-16(27-12(2)23)20(3,4)17(21)15(25)10-22(18,9-13)19(11)26/h13-18,24-25H,1,6-10H2,2-5H3/t13-,14+,15+,16+,17-,18+,21-,22+/m1/s1
InChI Key AFWHPJJUZOPPFV-FQQBCUCGSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C22H32O5
Molecular Weight 376.50 g/mol
Exact Mass 376.22497412 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.64
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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CHEMBL225489

2D Structure

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2D Structure of Inflexanin A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9861 98.61%
Caco-2 - 0.5725 57.25%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7350 73.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8294 82.94%
OATP1B3 inhibitior - 0.3600 36.00%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7932 79.32%
P-glycoprotein inhibitior - 0.7100 71.00%
P-glycoprotein substrate - 0.7683 76.83%
CYP3A4 substrate + 0.7174 71.74%
CYP2C9 substrate - 0.7947 79.47%
CYP2D6 substrate - 0.8731 87.31%
CYP3A4 inhibition - 0.8121 81.21%
CYP2C9 inhibition - 0.8036 80.36%
CYP2C19 inhibition - 0.8894 88.94%
CYP2D6 inhibition - 0.9291 92.91%
CYP1A2 inhibition - 0.7644 76.44%
CYP2C8 inhibition - 0.7745 77.45%
CYP inhibitory promiscuity - 0.8977 89.77%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6538 65.38%
Eye corrosion - 0.9934 99.34%
Eye irritation - 0.9267 92.67%
Skin irritation + 0.6165 61.65%
Skin corrosion - 0.9348 93.48%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5973 59.73%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5273 52.73%
skin sensitisation - 0.6041 60.41%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.7602 76.02%
Acute Oral Toxicity (c) III 0.5721 57.21%
Estrogen receptor binding + 0.8546 85.46%
Androgen receptor binding + 0.6517 65.17%
Thyroid receptor binding + 0.5683 56.83%
Glucocorticoid receptor binding + 0.8270 82.70%
Aromatase binding + 0.6947 69.47%
PPAR gamma - 0.5394 53.94%
Honey bee toxicity - 0.7277 72.77%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9972 99.72%

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 95.88% 96.09%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 95.39% 82.69%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.71% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.67% 91.11%
CHEMBL340 P08684 Cytochrome P450 3A4 88.17% 91.19%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.47% 93.04%
CHEMBL2581 P07339 Cathepsin D 85.42% 98.95%
CHEMBL259 P32245 Melanocortin receptor 4 84.84% 95.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.80% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.38% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.00% 100.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.50% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.54% 99.23%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.41% 97.14%
CHEMBL1902 P62942 FK506-binding protein 1A 81.18% 97.05%
CHEMBL5255 O00206 Toll-like receptor 4 80.58% 92.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.05% 95.56%

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.
Isodon excisus
Isodon inflexus

Cross-Links

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PubChem 13874229
LOTUS LTS0209803
wikiData Q104401647