N-methoxycarbonyl-4-(alpha-l-rhamnopyranosyloxy) benzylamine

Details

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Internal ID dd540eed-faab-4fa0-b48f-587bf25798f2
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name methyl N-[[4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]methyl]carbamate
SMILES (Canonical) CC1C(C(C(C(O1)OC2=CC=C(C=C2)CNC(=O)OC)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)OC2=CC=C(C=C2)CNC(=O)OC)O)O)O
InChI InChI=1S/C15H21NO7/c1-8-11(17)12(18)13(19)14(22-8)23-10-5-3-9(4-6-10)7-16-15(20)21-2/h3-6,8,11-14,17-19H,7H2,1-2H3,(H,16,20)/t8-,11-,12+,13+,14-/m0/s1
InChI Key VONHIBQETRIZNS-CNJBRALLSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H21NO7
Molecular Weight 327.33 g/mol
Exact Mass 327.13180201 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP -0.20
Atomic LogP (AlogP) -0.25
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N-methoxycarbonyl-4-(alpha-l-rhamnopyranosyloxy) benzylamine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5398 53.98%
Caco-2 - 0.7147 71.47%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.5283 52.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9441 94.41%
OATP1B3 inhibitior + 0.9346 93.46%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9050 90.50%
P-glycoprotein inhibitior - 0.8884 88.84%
P-glycoprotein substrate - 0.8382 83.82%
CYP3A4 substrate + 0.5570 55.70%
CYP2C9 substrate + 0.5837 58.37%
CYP2D6 substrate - 0.8348 83.48%
CYP3A4 inhibition - 0.7211 72.11%
CYP2C9 inhibition - 0.8891 88.91%
CYP2C19 inhibition - 0.7970 79.70%
CYP2D6 inhibition - 0.7381 73.81%
CYP1A2 inhibition - 0.8812 88.12%
CYP2C8 inhibition - 0.7517 75.17%
CYP inhibitory promiscuity - 0.6635 66.35%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.6377 63.77%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.9852 98.52%
Skin irritation - 0.7951 79.51%
Skin corrosion - 0.9484 94.84%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7068 70.68%
Micronuclear + 0.7400 74.00%
Hepatotoxicity - 0.6697 66.97%
skin sensitisation - 0.8691 86.91%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7667 76.67%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.8709 87.09%
Acute Oral Toxicity (c) III 0.5645 56.45%
Estrogen receptor binding - 0.6965 69.65%
Androgen receptor binding - 0.6718 67.18%
Thyroid receptor binding + 0.5547 55.47%
Glucocorticoid receptor binding - 0.7051 70.51%
Aromatase binding - 0.5061 50.61%
PPAR gamma - 0.5826 58.26%
Honey bee toxicity - 0.7805 78.05%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.4485 44.85%

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 97.98% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.79% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.34% 98.95%
CHEMBL4208 P20618 Proteasome component C5 92.04% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.53% 94.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.45% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 89.26% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.34% 96.00%
CHEMBL1944 P08473 Neprilysin 82.73% 92.63%
CHEMBL221 P23219 Cyclooxygenase-1 82.05% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.62% 95.56%
CHEMBL3437 Q16853 Amine oxidase, copper containing 80.53% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.16% 86.33%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 80.04% 89.67%

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.
Calamus draco
Excoecaria acerifolia
Garrya laurifolia
Goupia glabra
Laggera alata
Medinilla magnifica
Mesua ferrea
Moringa oleifera
Onobrychis bobrovii
Papaver persicum
Petteria ramentacea
Senecio cathcartensis
Sequoia sempervirens
Syncarpha gnaphaloides

Cross-Links

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PubChem 91101122
NPASS NPC131310
LOTUS LTS0073002
wikiData Q105290287