[(7R,9Z,11S,12R,13R,14S,15S,16R,17S,18R,19E,21E)-2,15,17,32-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-6,23-dioxo-8,33-dioxa-27-thia-24,29-diazapentacyclo[23.6.1.14,7.05,31.026,30]tritriaconta-1(31),2,4,9,19,21,25(32),26(30),28-nonaen-13-yl] acetate

Details

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Internal ID 9427f7d2-7a26-481b-bbc2-0ba635c377c2
Taxonomy Organoheterocyclic compounds > Naphthothiazoles
IUPAC Name [(7R,9Z,11S,12R,13R,14S,15S,16R,17S,18R,19E,21E)-2,15,17,32-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-6,23-dioxo-8,33-dioxa-27-thia-24,29-diazapentacyclo[23.6.1.14,7.05,31.026,30]tritriaconta-1(31),2,4,9,19,21,25(32),26(30),28-nonaen-13-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C38H46N2O11S/c1-16-11-10-12-17(2)37(47)40-28-32(45)25-24(27-35(28)52-15-39-27)26-34(21(6)31(25)44)51-38(8,36(26)46)49-14-13-23(48-9)18(3)33(50-22(7)41)20(5)30(43)19(4)29(16)42/h10-16,18-20,23,29-30,33,42-45H,1-9H3,(H,40,47)/b11-10+,14-13-,17-12+/t16-,18-,19-,20+,23+,29+,30+,33+,38-/m1/s1
InChI Key XTPGUQSTSWYULT-BUTBPWPRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C38H46N2O11S
Molecular Weight 738.80 g/mol
Exact Mass 738.28223146 g/mol
Topological Polar Surface Area (TPSA) 222.00 Ų
XlogP 6.30
Atomic LogP (AlogP) 5.66
H-Bond Acceptor 13
H-Bond Donor 5
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(7R,9Z,11S,12R,13R,14S,15S,16R,17S,18R,19E,21E)-2,15,17,32-tetrahydroxy-11-methoxy-3,7,12,14,16,18,22-heptamethyl-6,23-dioxo-8,33-dioxa-27-thia-24,29-diazapentacyclo[23.6.1.14,7.05,31.026,30]tritriaconta-1(31),2,4,9,19,21,25(32),26(30),28-nonaen-13-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7165 71.65%
Caco-2 - 0.8525 85.25%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Plasma membrane 0.4941 49.41%
OATP2B1 inhibitior - 0.5057 50.57%
OATP1B1 inhibitior + 0.7692 76.92%
OATP1B3 inhibitior + 0.9280 92.80%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.9891 98.91%
P-glycoprotein inhibitior - 0.5201 52.01%
P-glycoprotein substrate + 0.7851 78.51%
CYP3A4 substrate + 0.6940 69.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8910 89.10%
CYP3A4 inhibition - 0.5230 52.30%
CYP2C9 inhibition - 0.5783 57.83%
CYP2C19 inhibition - 0.5823 58.23%
CYP2D6 inhibition - 0.8729 87.29%
CYP1A2 inhibition - 0.7420 74.20%
CYP2C8 inhibition + 0.7922 79.22%
CYP inhibitory promiscuity + 0.6177 61.77%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8943 89.43%
Carcinogenicity (trinary) Non-required 0.4898 48.98%
Eye corrosion - 0.9863 98.63%
Eye irritation - 0.9139 91.39%
Skin irritation - 0.7893 78.93%
Skin corrosion - 0.9348 93.48%
Ames mutagenesis + 0.5763 57.63%
Human Ether-a-go-go-Related Gene inhibition - 0.3719 37.19%
Micronuclear + 0.8800 88.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation - 0.8526 85.26%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7817 78.17%
Acute Oral Toxicity (c) III 0.6288 62.88%
Estrogen receptor binding + 0.7998 79.98%
Androgen receptor binding + 0.7670 76.70%
Thyroid receptor binding + 0.5413 54.13%
Glucocorticoid receptor binding + 0.7757 77.57%
Aromatase binding + 0.6494 64.94%
PPAR gamma + 0.7862 78.62%
Honey bee toxicity - 0.6853 68.53%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9794 97.94%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 99.67% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 97.92% 99.23%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.65% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.44% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.36% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 97.01% 94.00%
CHEMBL3401 O75469 Pregnane X receptor 95.77% 94.73%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.77% 96.77%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 94.63% 93.40%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.33% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.07% 98.95%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 91.83% 81.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.06% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.92% 95.56%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 84.68% 94.42%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 84.31% 85.30%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 84.25% 93.10%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 83.58% 95.71%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.40% 95.50%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.81% 95.89%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 80.04% 99.15%
CHEMBL2095226 P05556 Integrin alpha-5/beta-1 80.00% 96.39%

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 162850581
LOTUS LTS0207201
wikiData Q105341754