N2'-Deacetyl-15-hydroxy-N2'-(2-methyl-1-oxopropyl)maytansine

Details

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Internal ID 673bfaa7-81b7-4685-90e5-580cd36f55a6
Taxonomy Phenylpropanoids and polyketides > Macrolactams
IUPAC Name (11-chloro-15,21-dihydroxy-12,20-dimethoxy-2,5,9,16-tetramethyl-8,23-dioxo-4,24-dioxa-9,22-diazatetracyclo[19.3.1.110,14.03,5]hexacosa-10,12,14(26),16,18-pentaen-6-yl) 2-[methyl(2-methylpropanoyl)amino]propanoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C36H50ClN3O11/c1-18(2)32(43)39(7)21(5)33(44)50-27-16-28(41)40(8)23-14-22(15-24(47-9)29(23)37)30(42)19(3)12-11-13-26(48-10)36(46)17-25(49-34(45)38-36)20(4)31-35(27,6)51-31/h11-15,18,20-21,25-27,30-31,42,46H,16-17H2,1-10H3,(H,38,45)
InChI Key CJFMMFRLGXTVGK-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C36H50ClN3O11
Molecular Weight 736.20 g/mol
Exact Mass 735.3133871 g/mol
Topological Polar Surface Area (TPSA) 177.00 Ų
XlogP 1.90
Atomic LogP (AlogP) 3.66
H-Bond Acceptor 11
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N2'-Deacetyl-15-hydroxy-N2'-(2-methyl-1-oxopropyl)maytansine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9241 92.41%
Caco-2 - 0.8389 83.89%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Lysosomes 0.5201 52.01%
OATP2B1 inhibitior + 0.7113 71.13%
OATP1B1 inhibitior + 0.8330 83.30%
OATP1B3 inhibitior + 0.9363 93.63%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.9815 98.15%
P-glycoprotein inhibitior + 0.7820 78.20%
P-glycoprotein substrate + 0.7943 79.43%
CYP3A4 substrate + 0.7447 74.47%
CYP2C9 substrate - 0.8092 80.92%
CYP2D6 substrate - 0.8485 84.85%
CYP3A4 inhibition - 0.9268 92.68%
CYP2C9 inhibition - 0.8908 89.08%
CYP2C19 inhibition - 0.8865 88.65%
CYP2D6 inhibition - 0.9194 91.94%
CYP1A2 inhibition - 0.8900 89.00%
CYP2C8 inhibition + 0.6445 64.45%
CYP inhibitory promiscuity - 0.7984 79.84%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.4331 43.31%
Eye corrosion - 0.9816 98.16%
Eye irritation - 0.9198 91.98%
Skin irritation - 0.7698 76.98%
Skin corrosion - 0.9191 91.91%
Ames mutagenesis - 0.5164 51.64%
Human Ether-a-go-go-Related Gene inhibition - 0.3785 37.85%
Micronuclear + 0.8000 80.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8384 83.84%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.9556 95.56%
Mitochondrial toxicity + 0.8875 88.75%
Nephrotoxicity - 0.8217 82.17%
Acute Oral Toxicity (c) III 0.5861 58.61%
Estrogen receptor binding + 0.8198 81.98%
Androgen receptor binding + 0.7784 77.84%
Thyroid receptor binding + 0.6229 62.29%
Glucocorticoid receptor binding + 0.8110 81.10%
Aromatase binding + 0.6750 67.50%
PPAR gamma + 0.8084 80.84%
Honey bee toxicity - 0.6020 60.20%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9777 97.77%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 99.57% 96.09%
CHEMBL1914 P06276 Butyrylcholinesterase 98.22% 95.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.76% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 96.87% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.25% 91.11%
CHEMBL261 P00915 Carbonic anhydrase I 96.23% 96.76%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.87% 95.56%
CHEMBL220 P22303 Acetylcholinesterase 94.00% 94.45%
CHEMBL2581 P07339 Cathepsin D 93.54% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.43% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 93.06% 94.00%
CHEMBL204 P00734 Thrombin 92.52% 96.01%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.35% 95.89%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 91.06% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 90.73% 96.47%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 90.69% 98.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.63% 97.14%
CHEMBL3401 O75469 Pregnane X receptor 88.96% 94.73%
CHEMBL340 P08684 Cytochrome P450 3A4 88.37% 91.19%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.70% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.90% 97.25%
CHEMBL4208 P20618 Proteasome component C5 86.51% 90.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.48% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.89% 92.62%
CHEMBL1937 Q92769 Histone deacetylase 2 84.66% 94.75%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 84.14% 96.77%
CHEMBL2535 P11166 Glucose transporter 83.60% 98.75%
CHEMBL5314 Q06418 Tyrosine-protein kinase receptor TYRO3 82.40% 96.00%
CHEMBL2007625 O75874 Isocitrate dehydrogenase [NADP] cytoplasmic 82.16% 99.00%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 81.97% 91.03%
CHEMBL2413 P32246 C-C chemokine receptor type 1 81.33% 89.50%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.70% 89.00%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 80.30% 85.11%

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.
Colubrina texensis

Cross-Links

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PubChem 426671
LOTUS LTS0153424
wikiData Q104960993