General Information

MaintermTHIOUREA--PROHIBITED
Doc TypeBAN
CAS Reg.No.(or other ID)62-56-6
Regnum 189.190

From www.fda.gov

Computed Descriptors

Download SDF
2D Structure
CID2723790
IUPAC Namethiourea
InChIInChI=1S/CH4N2S/c2-1(3)4/h(H4,2,3,4)
InChI KeyUMGDCJDMYOKAJW-UHFFFAOYSA-N
Canonical SMILESC(=S)(N)N
Molecular FormulaCH4N2S
Wikipediathiourea

From Pubchem


Computed Properties

Property Name Property Value
Molecular Weight76.117
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Complexity29.0
CACTVS Substructure Key Fingerprint A A A D c Y A D A A B A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A B A Q Q A A A A A A A A A A A B A A B A A A A E A A A A A A A A A A A A A A E A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A A = =
Topological Polar Surface Area84.1
Monoisotopic Mass76.01
Exact Mass76.01
XLogP3None
XLogP3-AA-0.8
Compound Is CanonicalizedTrue
Formal Charge0
Heavy Atom Count4
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Isotope Atom Count0
Covalently-Bonded Unit Count1

From Pubchem


ADMET Predicted Profile --- Classification

Model Result Probability
Absorption
Blood-Brain BarrierBBB+0.8912
Human Intestinal AbsorptionHIA+0.8750
Caco-2 PermeabilityCaco2-0.6739
P-glycoprotein SubstrateNon-substrate0.8850
P-glycoprotein InhibitorNon-inhibitor0.9659
Non-inhibitor0.9911
Renal Organic Cation TransporterNon-inhibitor0.9208
Distribution
Subcellular localizationLysosome0.7130
Metabolism
CYP450 2C9 SubstrateNon-substrate0.8293
CYP450 2D6 SubstrateNon-substrate0.7747
CYP450 3A4 SubstrateNon-substrate0.8692
CYP450 1A2 InhibitorNon-inhibitor0.7773
CYP450 2C9 InhibitorNon-inhibitor0.7438
CYP450 2D6 InhibitorNon-inhibitor0.9696
CYP450 2C19 InhibitorNon-inhibitor0.8765
CYP450 3A4 InhibitorNon-inhibitor0.9049
CYP Inhibitory PromiscuityLow CYP Inhibitory Promiscuity0.8547
Excretion
Toxicity
Human Ether-a-go-go-Related Gene InhibitionWeak inhibitor0.9793
Non-inhibitor0.9680
AMES ToxicityNon AMES toxic0.9708
CarcinogensNon-carcinogens0.7402
Fish ToxicityHigh FHMT0.6397
Tetrahymena Pyriformis ToxicityHigh TPT0.6988
Honey Bee ToxicityHigh HBT0.6980
BiodegradationNot ready biodegradable0.7962
Acute Oral ToxicityII0.7109
Carcinogenicity (Three-class)Non-required0.5253

From admetSAR


ADMET Predicted Profile --- Regression

Model Value Unit
Absorption
Aqueous solubility0.2573LogS
Caco-2 Permeability0.8903LogPapp, cm/s
Distribution
Metabolism
Excretion
Toxicity
Rat Acute Toxicity3.1168LD50, mol/kg
Fish Toxicity2.4468pLC50, mg/L
Tetrahymena Pyriformis Toxicity0.3966pIGC50, ug/L

From admetSAR


Toxicity Profile

Route of Exposure
Mechanism of Toxicity
Metabolism
Toxicity Values
Lethal Dose
Carcinogenicity (IARC Classification)3, not classifiable as to its carcinogenicity to humans.
Minimum Risk Level
Health Effects
Treatment
Reference
  1. Chen MH, Chen Z, Song BA, Bhadury PS, Yang S, Cai XJ, Hu DY, Xue W, Zeng S: Synthesis and antiviral activities of chiral thiourea derivatives containing an alpha-aminophosphonate moiety. J Agric Food Chem. 2009 Feb 25;57(4):1383-8. doi: 10.1021/jf803215t.[19199594 ]
  2. Shankar V, Pandeya SN: Synthesis of a series of new N1-[4-(4-nitrophenylthio)phenyl]-N3-(H/alkyl/acyl/aryl) thioureas and their antifungal, insecticidal and larvicidal activities. Arzneimittelforschung. 1981;31(5):753-6.[7196731 ]
  3. Vogelpoel FR, van Kooij RJ, te Velde ER, Verhoef J: Influence of polymorphonuclear granulocytes on the zona-free hamster oocyte assay. Hum Reprod. 1991 Sep;6(8):1104-7.[1806570 ]

From T3DB


Taxonomic Classification

KingdomOrganic compounds
SuperclassOrganosulfur compounds
ClassThioureas
SubclassNot available
Intermediate Tree NodesNot available
Direct ParentThioureas
Alternative Parents
Molecular FrameworkAliphatic acyclic compounds
SubstituentsThiourea - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aliphatic acyclic compound
DescriptionThis compound belongs to the class of organic compounds known as thioureas. These are organic compounds containing the thiourea functional group, a derivative of urea with the general structure (R1(N)R2C(=S)(R3)R4, R1-R4=H, alkyl, aryl), obtained by replacing the carbonyl group of urea with a thiocarbonyl group.

From ClassyFire


Targets

General Function:
Zinc ion binding
Specific Function:
Nuclear hormone receptor. The steroid hormones and their receptors are involved in the regulation of eukaryotic gene expression and affect cellular proliferation and differentiation in target tissues. Ligand-dependent nuclear transactivation involves either direct homodimer binding to a palindromic estrogen response element (ERE) sequence or association with other DNA-binding transcription factors, such as AP-1/c-Jun, c-Fos, ATF-2, Sp1 and Sp3, to mediate ERE-independent signaling. Ligand binding induces a conformational change allowing subsequent or combinatorial association with multiprotein coactivator complexes through LXXLL motifs of their respective components. Mutual transrepression occurs between the estrogen receptor (ER) and NF-kappa-B in a cell-type specific manner. Decreases NF-kappa-B DNA-binding activity and inhibits NF-kappa-B-mediated transcription from the IL6 promoter and displace RELA/p65 and associated coregulators from the promoter. Recruited to the NF-kappa-B response element of the CCL2 and IL8 promoters and can displace CREBBP. Present with NF-kappa-B components RELA/p65 and NFKB1/p50 on ERE sequences. Can also act synergistically with NF-kappa-B to activate transcription involving respective recruitment adjacent response elements; the function involves CREBBP. Can activate the transcriptional activity of TFF1. Also mediates membrane-initiated estrogen signaling involving various kinase cascades. Isoform 3 is involved in activation of NOS3 and endothelial nitric oxide production. Isoforms lacking one or several functional domains are thought to modulate transcriptional activity by competitive ligand or DNA binding and/or heterodimerization with the full length receptor. Essential for MTA1-mediated transcriptional regulation of BRCA1 and BCAS3. Isoform 3 can bind to ERE and inhibit isoform 1.
Gene Name:
ESR1
Uniprot ID:
P03372
Molecular Weight:
66215.45 Da
References
  1. Sipes NS, Martin MT, Kothiya P, Reif DM, Judson RS, Richard AM, Houck KA, Dix DJ, Kavlock RJ, Knudsen TB: Profiling 976 ToxCast chemicals across 331 enzymatic and receptor signaling assays. Chem Res Toxicol. 2013 Jun 17;26(6):878-95. doi: 10.1021/tx400021f. Epub 2013 May 16. [23611293 ]

From T3DB