Brunfelsamidine

Details

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Internal ID fcfe3e1e-fc71-451f-ae2f-6b09fc506b60
Taxonomy Organoheterocyclic compounds > Pyrroles > Substituted pyrroles
IUPAC Name 1H-pyrrole-3-carboximidamide
SMILES (Canonical) C1=CNC=C1C(=N)N
SMILES (Isomeric) C1=CNC=C1C(=N)N
InChI InChI=1S/C5H7N3/c6-5(7)4-1-2-8-3-4/h1-3,8H,(H3,6,7)
InChI Key XVEVWOAHSYZRQE-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H7N3
Molecular Weight 109.13 g/mol
Exact Mass 109.063997236 g/mol
Topological Polar Surface Area (TPSA) 65.70 Ų
XlogP -0.30
Atomic LogP (AlogP) 0.30
H-Bond Acceptor 1
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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1H-Pyrrole-3-carboximidamide
97744-98-4
FT2DW4V2WG
C10133
AC1NQYW1
pyrrol-3-ylidenemethanediamine
1H-Pyrrole-3-carboximindamide
HOPAMIDINE
pyrrole-3-carbamidine
UNII-FT2DW4V2WG
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Brunfelsamidine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9881 98.81%
Caco-2 + 0.8477 84.77%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Lysosomes 0.7342 73.42%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9792 97.92%
OATP1B3 inhibitior + 0.9490 94.90%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.9288 92.88%
P-glycoprotein inhibitior - 0.9891 98.91%
P-glycoprotein substrate - 0.9009 90.09%
CYP3A4 substrate - 0.7919 79.19%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8789 87.89%
CYP3A4 inhibition - 0.9421 94.21%
CYP2C9 inhibition - 0.9434 94.34%
CYP2C19 inhibition - 0.9160 91.60%
CYP2D6 inhibition - 0.9628 96.28%
CYP1A2 inhibition - 0.9010 90.10%
CYP2C8 inhibition - 0.9607 96.07%
CYP inhibitory promiscuity - 0.9353 93.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7700 77.00%
Carcinogenicity (trinary) Non-required 0.4844 48.44%
Eye corrosion - 0.9146 91.46%
Eye irritation + 0.9563 95.63%
Skin irritation + 0.5115 51.15%
Skin corrosion + 0.5231 52.31%
Ames mutagenesis - 0.8478 84.78%
Human Ether-a-go-go-Related Gene inhibition - 0.7422 74.22%
Micronuclear + 0.7600 76.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8309 83.09%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.7111 71.11%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7658 76.58%
Acute Oral Toxicity (c) II 0.5291 52.91%
Estrogen receptor binding - 0.9464 94.64%
Androgen receptor binding - 0.8922 89.22%
Thyroid receptor binding - 0.6924 69.24%
Glucocorticoid receptor binding - 0.8901 89.01%
Aromatase binding - 0.7682 76.82%
PPAR gamma - 0.8386 83.86%
Honey bee toxicity - 0.9622 96.22%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.9275 92.75%

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
CHEMBL3286 P00749 Urokinase-type plasminogen activator 91.40% 97.88%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.84% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.22% 95.56%

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.
Brunfelsia grandiflora
Nierembergia linariifolia

Cross-Links

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PubChem 176662
LOTUS LTS0118651
wikiData Q19903618