22-hydroxylshearinine F

Details

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Internal ID db1b5399-a9f6-42cb-a1b1-7481be2bffa4
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name (1S,4R,5S,17R,23S,26S,30R)-17,26-dihydroxy-4,5,13,13,15,15,31,31-octamethyl-14,32,33-trioxa-7-azanonacyclo[28.2.1.01,27.04,26.05,23.06,21.08,20.010,18.011,16]tritriaconta-6(21),8,10(18),11(16),19,27-hexaen-29-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C37H45NO6/c1-31(2)17-23-19-15-24-20(14-21(19)28(40)27(23)32(3,4)43-31)22-13-18-9-10-36(41)26-16-25(39)30-33(5,6)44-37(26,42-30)12-11-34(36,7)35(18,8)29(22)38-24/h14-16,18,28,30,38,40-41H,9-13,17H2,1-8H3/t18-,28+,30-,34+,35+,36+,37-/m0/s1
InChI Key VXLPYBLSZWNTJE-AIUUMKESSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C37H45NO6
Molecular Weight 599.80 g/mol
Exact Mass 599.32468816 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 6.10
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 22-hydroxylshearinine F

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 - 0.7742 77.42%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5130 51.30%
OATP2B1 inhibitior - 0.7095 70.95%
OATP1B1 inhibitior + 0.8403 84.03%
OATP1B3 inhibitior + 0.9158 91.58%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7821 78.21%
BSEP inhibitior + 0.9820 98.20%
P-glycoprotein inhibitior + 0.7670 76.70%
P-glycoprotein substrate + 0.7030 70.30%
CYP3A4 substrate + 0.7266 72.66%
CYP2C9 substrate - 0.7935 79.35%
CYP2D6 substrate - 0.8501 85.01%
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 + 0.6745 67.45%
CYP inhibitory promiscuity - 0.7642 76.42%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.4686 46.86%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9099 90.99%
Skin irritation - 0.6809 68.09%
Skin corrosion - 0.9252 92.52%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5569 55.69%
Micronuclear - 0.5700 57.00%
Hepatotoxicity - 0.6092 60.92%
skin sensitisation - 0.8042 80.42%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9125 91.25%
Nephrotoxicity + 0.5114 51.14%
Acute Oral Toxicity (c) III 0.5451 54.51%
Estrogen receptor binding + 0.7736 77.36%
Androgen receptor binding + 0.7562 75.62%
Thyroid receptor binding + 0.6499 64.99%
Glucocorticoid receptor binding + 0.8109 81.09%
Aromatase binding + 0.7607 76.07%
PPAR gamma + 0.7071 70.71%
Honey bee toxicity - 0.6709 67.09%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity + 0.5800 58.00%
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 99.50% 91.11%
CHEMBL4040 P28482 MAP kinase ERK2 98.58% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.49% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.87% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.55% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.16% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 94.57% 97.25%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.38% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.32% 95.56%
CHEMBL1902 P62942 FK506-binding protein 1A 92.58% 97.05%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 91.72% 93.40%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.42% 100.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.91% 92.94%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 89.38% 93.04%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.27% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 88.94% 97.09%
CHEMBL279 P35968 Vascular endothelial growth factor receptor 2 88.51% 95.52%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.23% 99.23%
CHEMBL3922 P50579 Methionine aminopeptidase 2 86.93% 97.28%
CHEMBL213 P08588 Beta-1 adrenergic receptor 85.55% 95.56%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 84.67% 92.88%
CHEMBL1163125 O60885 Bromodomain-containing protein 4 83.65% 97.31%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 83.37% 94.23%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.68% 96.38%
CHEMBL1937 Q92769 Histone deacetylase 2 82.07% 94.75%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.05% 91.07%
CHEMBL3192 Q9BY41 Histone deacetylase 8 81.69% 93.99%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 80.75% 96.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.12% 92.62%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139590472
LOTUS LTS0069810
wikiData Q105298564