6-Hydroxylpaspalinine

Details

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Internal ID 4655631b-f03b-4dae-a855-9751118a8044
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (1R,2R,4S,5S,16S,19R,23R)-2-hydroxy-4,5,24,24-tetramethyl-25,26-dioxa-7-azaheptacyclo[21.2.1.01,20.04,19.05,16.06,14.08,13]hexacosa-6(14),8,10,12,20-pentaen-22-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H31NO4/c1-24(2)23-20(29)12-18-17-10-9-14-11-16-15-7-5-6-8-19(15)28-22(16)26(14,4)25(17,3)13-21(30)27(18,31-23)32-24/h5-8,12,14,17,21,23,28,30H,9-11,13H2,1-4H3/t14-,17-,21+,23-,25-,26+,27+/m0/s1
InChI Key SMUWWVMLCRYVKW-GOJHYGRYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H31NO4
Molecular Weight 433.50 g/mol
Exact Mass 433.22530847 g/mol
Topological Polar Surface Area (TPSA) 71.60 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.18
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Hydroxylpaspalinine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9887 98.87%
Caco-2 - 0.5203 52.03%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.5130 51.30%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.8123 81.23%
OATP1B3 inhibitior + 0.9158 91.58%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7821 78.21%
BSEP inhibitior + 0.9012 90.12%
P-glycoprotein inhibitior - 0.4700 47.00%
P-glycoprotein substrate + 0.5600 56.00%
CYP3A4 substrate + 0.7048 70.48%
CYP2C9 substrate - 0.7855 78.55%
CYP2D6 substrate - 0.8540 85.40%
CYP3A4 inhibition - 0.8437 84.37%
CYP2C9 inhibition - 0.8740 87.40%
CYP2C19 inhibition - 0.8786 87.86%
CYP2D6 inhibition - 0.9256 92.56%
CYP1A2 inhibition + 0.8027 80.27%
CYP2C8 inhibition + 0.6144 61.44%
CYP inhibitory promiscuity - 0.7642 76.42%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4686 46.86%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9640 96.40%
Skin irritation - 0.6809 68.09%
Skin corrosion - 0.9252 92.52%
Ames mutagenesis - 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7660 76.60%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8042 80.42%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.4603 46.03%
Acute Oral Toxicity (c) III 0.5451 54.51%
Estrogen receptor binding + 0.8726 87.26%
Androgen receptor binding + 0.7011 70.11%
Thyroid receptor binding + 0.7520 75.20%
Glucocorticoid receptor binding + 0.8135 81.35%
Aromatase binding + 0.7437 74.37%
PPAR gamma + 0.6752 67.52%
Honey bee toxicity - 0.8105 81.05%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9889 98.89%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.17% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.59% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.04% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.82% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.48% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.33% 89.00%
CHEMBL2581 P07339 Cathepsin D 91.79% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 91.65% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 91.51% 99.23%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.14% 94.45%
CHEMBL3310 Q96DB2 Histone deacetylase 11 87.83% 88.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.37% 95.89%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 85.23% 94.23%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 84.72% 94.62%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.33% 94.00%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 83.73% 95.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.85% 100.00%
CHEMBL4523377 Q86WV6 Stimulator of interferon genes protein 80.88% 95.48%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.25% 92.62%

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.
There are no matching plants.

Cross-Links

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PubChem 139590473
LOTUS LTS0064913
wikiData Q105256179