4|A-Hydroxy-10-DAB

Details

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Internal ID b3c760c9-aec7-4196-9168-ede163d9ea21
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Taxanes and derivatives
IUPAC Name [(1R,2S,3R,4S,7R,9S,10S,12R,15R,16S)-4-acetyloxy-1,9,12,15,16-pentahydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate
SMILES (Canonical) CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(C(C1O)O)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)C)O
SMILES (Isomeric) CC1=C2[C@H](C(=O)[C@@]3([C@H](C[C@@H]4[C@]([C@H]3[C@@H]([C@@](C2(C)C)([C@H]([C@@H]1O)O)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)C)O
InChI InChI=1S/C29H36O11/c1-13-18-20(33)22(34)27(5)16(31)11-17-28(12-38-17,40-14(2)30)21(27)24(39-25(36)15-9-7-6-8-10-15)29(37,26(18,3)4)23(35)19(13)32/h6-10,16-17,19-21,23-24,31-33,35,37H,11-12H2,1-5H3/t16-,17+,19+,20+,21-,23-,24-,27+,28-,29+/m0/s1
InChI Key FNZPZCTVRVPPAB-YZSQHPIKSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H36O11
Molecular Weight 560.60 g/mol
Exact Mass 560.22576196 g/mol
Topological Polar Surface Area (TPSA) 180.00 Ų
XlogP -0.40
Atomic LogP (AlogP) 0.05
H-Bond Acceptor 11
H-Bond Donor 5
Rotatable Bonds 3

Synonyms

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4|A-Hydroxy-10-DAB
[(1R,2S,3R,4S,7R,9S,10S,12R,15R,16S)-4-Acetyloxy-1,9,12,15,16-pentahydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate
SCHEMBL14484263
DTXSID00415736
10-Deacetyl-14beta-hydroxybaccatin III
(1R,2S,3R,4S,7R,9S,10S,12R,15R,16S)-4-(acetyloxy)-1,9,12,15,16-pentahydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.0,.0,heptadec-13-en-2-yl benzoate

2D Structure

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2D Structure of 4|A-Hydroxy-10-DAB

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9584 95.84%
Caco-2 - 0.7840 78.40%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.7722 77.22%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.7855 78.55%
OATP1B3 inhibitior + 0.9179 91.79%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6214 62.14%
P-glycoprotein inhibitior + 0.7040 70.40%
P-glycoprotein substrate + 0.7177 71.77%
CYP3A4 substrate + 0.7040 70.40%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8708 87.08%
CYP3A4 inhibition - 0.8346 83.46%
CYP2C9 inhibition - 0.7815 78.15%
CYP2C19 inhibition - 0.8345 83.45%
CYP2D6 inhibition - 0.8811 88.11%
CYP1A2 inhibition - 0.7329 73.29%
CYP2C8 inhibition + 0.8503 85.03%
CYP inhibitory promiscuity - 0.9128 91.28%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.4746 47.46%
Eye corrosion - 0.9876 98.76%
Eye irritation - 0.9072 90.72%
Skin irritation - 0.6777 67.77%
Skin corrosion - 0.9356 93.56%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7465 74.65%
Micronuclear - 0.5100 51.00%
Hepatotoxicity + 0.6578 65.78%
skin sensitisation - 0.7372 73.72%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity + 0.6722 67.22%
Acute Oral Toxicity (c) III 0.6114 61.14%
Estrogen receptor binding + 0.7822 78.22%
Androgen receptor binding + 0.7560 75.60%
Thyroid receptor binding + 0.5535 55.35%
Glucocorticoid receptor binding + 0.6504 65.04%
Aromatase binding + 0.6631 66.31%
PPAR gamma + 0.6450 64.50%
Honey bee toxicity - 0.7226 72.26%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.6000 60.00%
Fish aquatic toxicity + 0.9899 98.99%

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
CHEMBL221 P23219 Cyclooxygenase-1 95.65% 90.17%
CHEMBL2581 P07339 Cathepsin D 95.41% 98.95%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 95.39% 81.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.21% 86.33%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 93.78% 87.67%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.67% 94.62%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.92% 96.09%
CHEMBL2716 Q8WUI4 Histone deacetylase 7 90.28% 89.44%
CHEMBL5028 O14672 ADAM10 89.96% 97.50%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.92% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.67% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 89.59% 95.50%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 88.82% 83.00%
CHEMBL1951 P21397 Monoamine oxidase A 87.82% 91.49%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.94% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 86.60% 91.19%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.46% 97.09%
CHEMBL4208 P20618 Proteasome component C5 83.70% 90.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.67% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.92% 85.14%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.22% 90.24%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.23% 96.95%

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.
Taxus wallichiana

Cross-Links

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PubChem 5318183
NPASS NPC305902