(4R,4aS,5aR,6S,12aR)-7-chloro-4-(dimethylamino)-1,4a,6,10,11,12a-hexahydroxy-8-methoxy-6-methyl-3,12-dioxo-5,5a-dihydro-4H-tetracene-2-carboxamide

Details

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Internal ID a2ffed7d-b68d-45cc-87c3-38b49fc0f6eb
Taxonomy Phenylpropanoids and polyketides > Tetracyclines
IUPAC Name (4R,4aS,5aR,6S,12aR)-7-chloro-4-(dimethylamino)-1,4a,6,10,11,12a-hexahydroxy-8-methoxy-6-methyl-3,12-dioxo-5,5a-dihydro-4H-tetracene-2-carboxamide
SMILES (Canonical) CC1(C2CC3(C(C(=O)C(=C(C3(C(=O)C2=C(C4=C1C(=C(C=C4O)OC)Cl)O)O)O)C(=O)N)N(C)C)O)O
SMILES (Isomeric) C[C@@]1([C@@H]2C[C@@]3([C@H](C(=O)C(=C([C@@]3(C(=O)C2=C(C4=C1C(=C(C=C4O)OC)Cl)O)O)O)C(=O)N)N(C)C)O)O
InChI InChI=1S/C23H25ClN2O10/c1-21(33)7-6-22(34)17(26(2)3)16(29)12(20(25)32)19(31)23(22,35)18(30)10(7)15(28)11-8(27)5-9(36-4)14(24)13(11)21/h5,7,17,27-28,31,33-35H,6H2,1-4H3,(H2,25,32)/t7-,17+,21+,22+,23-/m1/s1
InChI Key ZFQSAYKGPAHJBK-SDPQGDBNSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C23H25ClN2O10
Molecular Weight 524.90 g/mol
Exact Mass 524.1197727 g/mol
Topological Polar Surface Area (TPSA) 211.00 Ų
XlogP -0.20
Atomic LogP (AlogP) -0.59
H-Bond Acceptor 11
H-Bond Donor 7
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (4R,4aS,5aR,6S,12aR)-7-chloro-4-(dimethylamino)-1,4a,6,10,11,12a-hexahydroxy-8-methoxy-6-methyl-3,12-dioxo-5,5a-dihydro-4H-tetracene-2-carboxamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9625 96.25%
Caco-2 - 0.6249 62.49%
Blood Brain Barrier - 1.0000 100.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6878 68.78%
OATP2B1 inhibitior - 0.8085 80.85%
OATP1B1 inhibitior + 0.8967 89.67%
OATP1B3 inhibitior + 0.9443 94.43%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5178 51.78%
P-glycoprotein inhibitior - 0.6642 66.42%
P-glycoprotein substrate + 0.5473 54.73%
CYP3A4 substrate + 0.6967 69.67%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8166 81.66%
CYP3A4 inhibition - 0.8586 85.86%
CYP2C9 inhibition - 0.8670 86.70%
CYP2C19 inhibition - 0.8493 84.93%
CYP2D6 inhibition - 0.9096 90.96%
CYP1A2 inhibition - 0.8470 84.70%
CYP2C8 inhibition - 0.6523 65.23%
CYP inhibitory promiscuity - 0.6387 63.87%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6100 61.00%
Eye corrosion - 0.9873 98.73%
Eye irritation - 0.9346 93.46%
Skin irritation - 0.7685 76.85%
Skin corrosion - 0.9192 91.92%
Ames mutagenesis - 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4691 46.91%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.8394 83.94%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.9250 92.50%
Nephrotoxicity + 0.6607 66.07%
Acute Oral Toxicity (c) III 0.5662 56.62%
Estrogen receptor binding + 0.6372 63.72%
Androgen receptor binding + 0.7281 72.81%
Thyroid receptor binding + 0.5651 56.51%
Glucocorticoid receptor binding + 0.6461 64.61%
Aromatase binding + 0.6638 66.38%
PPAR gamma + 0.6187 61.87%
Honey bee toxicity - 0.8433 84.33%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9772 97.72%

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 99.63% 91.11%
CHEMBL261 P00915 Carbonic anhydrase I 97.66% 96.76%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.79% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.51% 96.09%
CHEMBL340 P08684 Cytochrome P450 3A4 94.33% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 93.80% 92.94%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.12% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.81% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.35% 97.09%
CHEMBL205 P00918 Carbonic anhydrase II 90.28% 98.44%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 89.54% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.36% 95.89%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 87.14% 96.21%
CHEMBL1937 Q92769 Histone deacetylase 2 86.56% 94.75%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 85.30% 91.03%
CHEMBL2581 P07339 Cathepsin D 85.28% 98.95%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.81% 94.42%
CHEMBL4208 P20618 Proteasome component C5 83.05% 90.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.94% 86.92%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 82.86% 96.00%
CHEMBL204 P00734 Thrombin 82.03% 96.01%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.74% 97.14%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.66% 92.88%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 81.35% 91.07%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.26% 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.
There are no matching plants.

Cross-Links

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PubChem 101685472
LOTUS LTS0276143
wikiData Q105374594