Smtp-7D

Details

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Internal ID 3d87b88e-9012-45de-aca9-82e45126c057
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Indolyl carboxylic acids and derivatives
IUPAC Name (2R)-2,5-bis[(2R,3R)-2-[(3E)-4,8-dimethylnona-3,7-dienyl]-3,5-dihydroxy-2-methyl-7-oxo-4,9-dihydro-3H-pyrano[2,3-e]isoindol-8-yl]pentanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C51H68N2O10/c1-30(2)14-9-16-32(5)18-11-21-50(7)43(56)26-36-41(54)24-34-38(45(36)62-50)28-52(47(34)58)23-13-20-40(49(60)61)53-29-39-35(48(53)59)25-42(55)37-27-44(57)51(8,63-46(37)39)22-12-19-33(6)17-10-15-31(3)4/h14-15,18-19,24-25,40,43-44,54-57H,9-13,16-17,20-23,26-29H2,1-8H3,(H,60,61)/b32-18+,33-19+/t40-,43-,44-,50-,51-/m1/s1
InChI Key CRNDCHORWGDFGR-VXZLMINMSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C51H68N2O10
Molecular Weight 869.10 g/mol
Exact Mass 868.48739637 g/mol
Topological Polar Surface Area (TPSA) 177.00 Ų
XlogP 8.90
Atomic LogP (AlogP) 9.00
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 18

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Smtp-7D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8929 89.29%
Caco-2 - 0.8479 84.79%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6430 64.30%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8382 83.82%
OATP1B3 inhibitior + 0.9144 91.44%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9863 98.63%
P-glycoprotein inhibitior + 0.7643 76.43%
P-glycoprotein substrate + 0.6407 64.07%
CYP3A4 substrate + 0.7012 70.12%
CYP2C9 substrate - 0.8106 81.06%
CYP2D6 substrate - 0.8380 83.80%
CYP3A4 inhibition - 0.8184 81.84%
CYP2C9 inhibition - 0.8733 87.33%
CYP2C19 inhibition - 0.7507 75.07%
CYP2D6 inhibition - 0.9421 94.21%
CYP1A2 inhibition - 0.8926 89.26%
CYP2C8 inhibition + 0.4629 46.29%
CYP inhibitory promiscuity - 0.9317 93.17%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.4315 43.15%
Eye corrosion - 0.9897 98.97%
Eye irritation - 0.9028 90.28%
Skin irritation - 0.7766 77.66%
Skin corrosion - 0.9325 93.25%
Ames mutagenesis - 0.6337 63.37%
Human Ether-a-go-go-Related Gene inhibition - 0.4067 40.67%
Micronuclear + 0.6900 69.00%
Hepatotoxicity - 0.5705 57.05%
skin sensitisation - 0.8701 87.01%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 1.0000 100.00%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity - 0.6626 66.26%
Acute Oral Toxicity (c) III 0.6566 65.66%
Estrogen receptor binding + 0.7945 79.45%
Androgen receptor binding + 0.7404 74.04%
Thyroid receptor binding + 0.5357 53.57%
Glucocorticoid receptor binding + 0.6780 67.80%
Aromatase binding + 0.5941 59.41%
PPAR gamma + 0.7492 74.92%
Honey bee toxicity - 0.7539 75.39%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9843 98.43%

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 99.37% 91.11%
CHEMBL2581 P07339 Cathepsin D 99.09% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.27% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 95.00% 93.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.63% 99.17%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.27% 89.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 90.95% 93.40%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.32% 86.33%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 89.54% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.21% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.41% 94.45%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.06% 92.08%
CHEMBL340 P08684 Cytochrome P450 3A4 85.22% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.05% 99.23%
CHEMBL1907 P15144 Aminopeptidase N 83.45% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 83.10% 94.73%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.07% 96.77%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.60% 99.15%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.29% 96.95%
CHEMBL3430907 Q96GD4 Aurora kinase B/Inner centromere protein 80.88% 97.50%

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 10418162
LOTUS LTS0154692
wikiData Q104968610