2-[(1S,2R,3'R,5S,7R,10S,11R,14R,15S,23S)-1',1',2,3',10,14,23-heptamethyl-18-sulfooxyspiro[6-oxahexacyclo[12.11.0.02,11.05,10.015,23.017,22]pentacosa-17,19,21-triene-7,2'-cyclohexane]-21-yl]-2-hydroxyacetic acid

Details

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Internal ID 4a66c613-6563-434a-92d3-e1c4a1ed4646
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name 2-[(1S,2R,3'R,5S,7R,10S,11R,14R,15S,23S)-1',1',2,3',10,14,23-heptamethyl-18-sulfooxyspiro[6-oxahexacyclo[12.11.0.02,11.05,10.015,23.017,22]pentacosa-17,19,21-triene-7,2'-cyclohexane]-21-yl]-2-hydroxyacetic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C38H56O8S/c1-22-9-8-15-33(2,3)38(22)20-19-36(6)27-12-16-35(5)26(34(27,4)18-14-29(36)45-38)13-17-37(7)28(35)21-24-25(46-47(42,43)44)11-10-23(30(24)37)31(39)32(40)41/h10-11,22,26-29,31,39H,8-9,12-21H2,1-7H3,(H,40,41)(H,42,43,44)/t22-,26-,27-,28+,29+,31?,34-,35-,36+,37+,38-/m1/s1
InChI Key XYEAFRXFNHUCSD-GKJVZBCHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C38H56O8S
Molecular Weight 672.90 g/mol
Exact Mass 672.36958991 g/mol
Topological Polar Surface Area (TPSA) 139.00 Ų
XlogP 8.70
Atomic LogP (AlogP) 7.81
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[(1S,2R,3'R,5S,7R,10S,11R,14R,15S,23S)-1',1',2,3',10,14,23-heptamethyl-18-sulfooxyspiro[6-oxahexacyclo[12.11.0.02,11.05,10.015,23.017,22]pentacosa-17,19,21-triene-7,2'-cyclohexane]-21-yl]-2-hydroxyacetic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9268 92.68%
Caco-2 - 0.8134 81.34%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5104 51.04%
OATP2B1 inhibitior - 0.5668 56.68%
OATP1B1 inhibitior + 0.8894 88.94%
OATP1B3 inhibitior + 0.9194 91.94%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9638 96.38%
P-glycoprotein inhibitior + 0.7872 78.72%
P-glycoprotein substrate + 0.5550 55.50%
CYP3A4 substrate + 0.7058 70.58%
CYP2C9 substrate - 0.8078 80.78%
CYP2D6 substrate - 0.8144 81.44%
CYP3A4 inhibition - 0.9001 90.01%
CYP2C9 inhibition - 0.8219 82.19%
CYP2C19 inhibition - 0.7632 76.32%
CYP2D6 inhibition - 0.8850 88.50%
CYP1A2 inhibition - 0.7154 71.54%
CYP2C8 inhibition + 0.6393 63.93%
CYP inhibitory promiscuity - 0.9223 92.23%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.5035 50.35%
Carcinogenicity (trinary) Non-required 0.6353 63.53%
Eye corrosion - 0.9631 96.31%
Eye irritation - 0.9165 91.65%
Skin irritation - 0.7552 75.52%
Skin corrosion - 0.8773 87.73%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3688 36.88%
Micronuclear + 0.5400 54.00%
Hepatotoxicity - 0.6823 68.23%
skin sensitisation - 0.8120 81.20%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity - 0.8534 85.34%
Acute Oral Toxicity (c) III 0.6235 62.35%
Estrogen receptor binding + 0.7274 72.74%
Androgen receptor binding + 0.7526 75.26%
Thyroid receptor binding - 0.5271 52.71%
Glucocorticoid receptor binding + 0.7630 76.30%
Aromatase binding + 0.7462 74.62%
PPAR gamma + 0.7029 70.29%
Honey bee toxicity - 0.7445 74.45%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6571 65.71%
Fish aquatic toxicity + 0.9970 99.70%

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 97.23% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.78% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.24% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.23% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.66% 97.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.30% 93.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.74% 95.89%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 88.18% 96.00%
CHEMBL340 P08684 Cytochrome P450 3A4 85.55% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.80% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.00% 100.00%
CHEMBL2179 P04062 Beta-glucocerebrosidase 83.47% 85.31%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.39% 89.00%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 82.12% 89.05%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.84% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.88% 99.23%
CHEMBL5028 O14672 ADAM10 80.38% 97.50%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 80.05% 91.03%

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 10770944
LOTUS LTS0154494
wikiData Q105344439