3',4'-Dideoxy-6'-C-methylbutirosin B

Details

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Internal ID 17d7cc54-3b52-471f-afb6-d39e58720e60
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > 2-deoxystreptamine aminoglycosides > 4,5-disubstituted 2-deoxystreptamines
IUPAC Name (2S)-4-amino-N-[5-amino-4-[3-amino-6-(1-aminoethyl)oxan-2-yl]oxy-3-[3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-hydroxycyclohexyl]-2-hydroxybutanamide
SMILES (Canonical) CC(C1CCC(C(O1)OC2C(CC(C(C2OC3C(C(C(O3)CO)O)O)O)NC(=O)C(CCN)O)N)N)N
SMILES (Isomeric) CC(C1CCC(C(O1)OC2C(CC(C(C2OC3C(C(C(O3)CO)O)O)O)NC(=O)[C@H](CCN)O)N)N)N
InChI InChI=1S/C22H43N5O10/c1-8(24)13-3-2-9(25)21(34-13)36-18-10(26)6-11(27-20(33)12(29)4-5-23)15(30)19(18)37-22-17(32)16(31)14(7-28)35-22/h8-19,21-22,28-32H,2-7,23-26H2,1H3,(H,27,33)/t8?,9?,10?,11?,12-,13?,14?,15?,16?,17?,18?,19?,21?,22?/m0/s1
InChI Key XPTQHPYRCFRZPX-VTXDMFHXSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C22H43N5O10
Molecular Weight 537.60 g/mol
Exact Mass 537.30099259 g/mol
Topological Polar Surface Area (TPSA) 271.00 Ų
XlogP -5.40
Atomic LogP (AlogP) -5.34
H-Bond Acceptor 14
H-Bond Donor 10
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3',4'-Dideoxy-6'-C-methylbutirosin B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9496 94.96%
Caco-2 - 0.8803 88.03%
Blood Brain Barrier - 0.9000 90.00%
Human oral bioavailability - 0.9286 92.86%
Subcellular localzation Mitochondria 0.4428 44.28%
OATP2B1 inhibitior - 0.8636 86.36%
OATP1B1 inhibitior + 0.8949 89.49%
OATP1B3 inhibitior + 0.9471 94.71%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9021 90.21%
P-glycoprotein inhibitior - 0.7497 74.97%
P-glycoprotein substrate - 0.6300 63.00%
CYP3A4 substrate + 0.6721 67.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8430 84.30%
CYP3A4 inhibition - 0.9111 91.11%
CYP2C9 inhibition - 0.9021 90.21%
CYP2C19 inhibition - 0.8877 88.77%
CYP2D6 inhibition - 0.9122 91.22%
CYP1A2 inhibition - 0.9400 94.00%
CYP2C8 inhibition - 0.6292 62.92%
CYP inhibitory promiscuity - 0.7542 75.42%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6719 67.19%
Eye corrosion - 0.9893 98.93%
Eye irritation - 0.9612 96.12%
Skin irritation - 0.7824 78.24%
Skin corrosion - 0.9313 93.13%
Ames mutagenesis - 0.7270 72.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4353 43.53%
Micronuclear + 0.7800 78.00%
Hepatotoxicity + 0.6670 66.70%
skin sensitisation - 0.8937 89.37%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.9375 93.75%
Nephrotoxicity + 0.5415 54.15%
Acute Oral Toxicity (c) III 0.5130 51.30%
Estrogen receptor binding + 0.5482 54.82%
Androgen receptor binding - 0.5254 52.54%
Thyroid receptor binding + 0.5282 52.82%
Glucocorticoid receptor binding + 0.6508 65.08%
Aromatase binding + 0.6446 64.46%
PPAR gamma + 0.6433 64.33%
Honey bee toxicity - 0.7298 72.98%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.9279 92.79%

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
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 99.67% 95.58%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.73% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.41% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 97.01% 97.09%
CHEMBL2094135 Q96BI3 Gamma-secretase 96.54% 98.05%
CHEMBL4040 P28482 MAP kinase ERK2 93.92% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.84% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.99% 97.25%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 92.84% 95.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 92.64% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.60% 99.17%
CHEMBL4581 P52732 Kinesin-like protein 1 92.35% 93.18%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 91.96% 96.38%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 91.31% 95.89%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 90.81% 96.47%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 90.00% 94.33%
CHEMBL226 P30542 Adenosine A1 receptor 89.98% 95.93%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 89.02% 96.77%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.43% 93.56%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 88.41% 96.21%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 87.46% 97.47%
CHEMBL4015 P41597 C-C chemokine receptor type 2 87.12% 98.57%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 86.92% 90.71%
CHEMBL2413 P32246 C-C chemokine receptor type 1 86.67% 89.50%
CHEMBL2514 O95665 Neurotensin receptor 2 86.62% 100.00%
CHEMBL2243 O00519 Anandamide amidohydrolase 86.36% 97.53%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 86.32% 91.03%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.15% 95.89%
CHEMBL3437 Q16853 Amine oxidase, copper containing 86.01% 94.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 85.77% 91.24%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.61% 96.95%
CHEMBL2581 P07339 Cathepsin D 85.41% 98.95%
CHEMBL237 P41145 Kappa opioid receptor 85.13% 98.10%
CHEMBL340 P08684 Cytochrome P450 3A4 82.77% 91.19%
CHEMBL218 P21554 Cannabinoid CB1 receptor 81.79% 96.61%
CHEMBL220 P22303 Acetylcholinesterase 80.77% 94.45%
CHEMBL2492 P36544 Neuronal acetylcholine receptor protein alpha-7 subunit 80.66% 88.42%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 80.66% 97.29%
CHEMBL2842 P42345 Serine/threonine-protein kinase mTOR 80.62% 92.78%
CHEMBL5255 O00206 Toll-like receptor 4 80.44% 92.50%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.33% 95.50%

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 139585625
LOTUS LTS0003427
wikiData Q77483857