Triptogelin A-1

Details

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Internal ID f15f94e5-4b1c-4129-913f-99012683ad33
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Pentacarboxylic acids and derivatives
IUPAC Name [(1S,2R,4S,5R,6S,7S,8R,9R,12R)-12-acetyloxy-5,7,8-tribenzoyloxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-4-yl] benzoate
SMILES (Canonical) CC1CC(C(C2(C13C(C(C(C2OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C(O3)(C)C)OC(=O)C)C)OC(=O)C6=CC=CC=C6)OC(=O)C7=CC=CC=C7
SMILES (Isomeric) C[C@@H]1C[C@@H]([C@@H]([C@@]2([C@]13[C@@H]([C@@H]([C@H]([C@H]2OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C(O3)(C)C)OC(=O)C)C)OC(=O)C6=CC=CC=C6)OC(=O)C7=CC=CC=C7
InChI InChI=1S/C45H44O11/c1-27-26-33(52-39(47)29-18-10-6-11-19-29)36(54-41(49)31-22-14-8-15-23-31)44(5)38(55-42(50)32-24-16-9-17-25-32)35(53-40(48)30-20-12-7-13-21-30)34-37(51-28(2)46)45(27,44)56-43(34,3)4/h6-25,27,33-38H,26H2,1-5H3/t27-,33+,34-,35-,36+,37-,38-,44+,45-/m1/s1
InChI Key KAMRIYILCXXILS-UHPPAMLESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C45H44O11
Molecular Weight 760.80 g/mol
Exact Mass 760.28836222 g/mol
Topological Polar Surface Area (TPSA) 141.00 Ų
XlogP 8.40
Atomic LogP (AlogP) 7.04
H-Bond Acceptor 11
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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132536-78-8
03173PR31Y
CCRIS 7111
UNII-03173PR31Y
TRIPTOGELIN A 1, (+)-
Q27896305
[(1S,2R,4S,5R,6S,7S,8R,9R,12R)-12-acetyloxy-5,7,8-tribenzoyloxy-2,6,10,10-tetramethyl-11-oxatricyclo[7.2.1.01,6]dodecan-4-yl] benzoate
2H-3,9A-METHANO-1-BENZOXEPIN-4,5,6,7,10-PENTOL, OCTAHYDRO-2,2,5A,9-TETRAMETHYL-, 10-ACETATE 4,5,6,7-TETRABENZOATE, (3R,4R,5S,5AS,6R,7S,9R,9AS,10R)-
2H-3,9A-METHANO-1-BENZOXEPIN-4,5,6,7,10-PENTOL, OCTAHYDRO-2,2,5A,9-TETRAMETHYL-, 10-ACETATE 4,5,6,7-TETRABENZOATE, (3R-(3.ALPHA.,4.ALPHA.,5.ALPHA.,5A.ALPHA.,6.ALPHA.,7.ALPHA.,9.ALPHA.,9A.ALPHA.,10R*))-

2D Structure

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2D Structure of Triptogelin A-1

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9830 98.30%
Caco-2 - 0.7644 76.44%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.5691 56.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8679 86.79%
OATP1B3 inhibitior + 0.9105 91.05%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9901 99.01%
P-glycoprotein inhibitior + 0.9455 94.55%
P-glycoprotein substrate - 0.7009 70.09%
CYP3A4 substrate + 0.6447 64.47%
CYP2C9 substrate - 0.8067 80.67%
CYP2D6 substrate - 0.8529 85.29%
CYP3A4 inhibition - 0.5272 52.72%
CYP2C9 inhibition - 0.7280 72.80%
CYP2C19 inhibition - 0.7022 70.22%
CYP2D6 inhibition - 0.9504 95.04%
CYP1A2 inhibition - 0.7799 77.99%
CYP2C8 inhibition + 0.5924 59.24%
CYP inhibitory promiscuity - 0.7653 76.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9343 93.43%
Carcinogenicity (trinary) Non-required 0.4262 42.62%
Eye corrosion - 0.9872 98.72%
Eye irritation - 0.8869 88.69%
Skin irritation - 0.8233 82.33%
Skin corrosion - 0.9338 93.38%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8556 85.56%
Micronuclear - 0.5826 58.26%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.7388 73.88%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.5222 52.22%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.7038 70.38%
Acute Oral Toxicity (c) III 0.4908 49.08%
Estrogen receptor binding + 0.8259 82.59%
Androgen receptor binding + 0.6729 67.29%
Thyroid receptor binding + 0.6813 68.13%
Glucocorticoid receptor binding + 0.7880 78.80%
Aromatase binding + 0.6080 60.80%
PPAR gamma + 0.7474 74.74%
Honey bee toxicity - 0.8258 82.58%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5345 53.45%
Fish aquatic toxicity + 0.9898 98.98%

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 93.85% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.77% 86.33%
CHEMBL2996 Q05655 Protein kinase C delta 93.35% 97.79%
CHEMBL2581 P07339 Cathepsin D 93.31% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.26% 96.09%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 90.29% 83.00%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.76% 94.62%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.10% 99.23%
CHEMBL1951 P21397 Monoamine oxidase A 88.89% 91.49%
CHEMBL221 P23219 Cyclooxygenase-1 88.76% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.12% 95.56%
CHEMBL5028 O14672 ADAM10 85.83% 97.50%
CHEMBL340 P08684 Cytochrome P450 3A4 85.45% 91.19%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 84.56% 94.08%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 84.35% 81.11%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 83.83% 97.14%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.96% 85.14%

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.
Tripterygium wilfordii

Cross-Links

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PubChem 14828974
LOTUS LTS0205823
wikiData Q27896305