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Compound InformationSONAR Target prediction
Name:

CARMUSTINE

Unique Identifier:SPE01503110
MolClass: Checkout models in ver1.5 and ver1.0
Molecular Formula:
Molecular Weight:204.978 g/mol
X log p:0.618  (online calculus)
Lipinksi Failures0
TPSA49.74
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptors Count:3
Rotatable Bond Count:7
Canonical Smiles:ClCCNC(=O)N(CCCl)N=O
Source:synthetic
Reference:Toxicol Appl Pharmacol 21: 405 (1972)
Therapeutics:antineoplastic, alkylating agent
Generic_name:Carmustine
Chemical_iupac_name:1,3-bis(2-chloroethyl)-1-nitroso-urea
Drug_type:Approved Drug
Pharmgkb_id:PA448810
Kegg_compound_id:C06873
Drugbank_id:APRD00006
Melting_point:31 oC
H2o_solubility:< 0.1 g/100 mL at 18 °C
Logp:1.256
Cas_registry_number:154-93-8
Drug_category:Antineoplastic Agents; ATC:L01AD01
Indication:For the treatment of brain tumors, multiple myeloma, Hodgkin-s disease and
Non-Hodgkin-s lymphomas.
Pharmacology:Carmustine is one of the nitrosoureas indicated as palliative therapy as a single
agent or in established combination therapy with other approved chemotherapeutic
agents in treatment of brain tumors, multiple myeloma, Hodgkin-s disease, and
non-Hodgkin-s lymphomas. Although it is generally agreed that carmustine alkylates
DNA and RNA, it is not cross resistant with other alkylators. As with other
nitrosoureas, it may also inhibit several key enzymatic processes by carbamoylation
of amino acids in proteins.
Mechanism_of_action:Carmustine causes cross-links in DNA and RNA, leading to the inhibition of DNA
synthesis, RNA production and RNA translation (protein synthesis). Carmustine also
binds to and modifies (carbamoylates) glutathione reductase. This leads to cell
death.
Organisms_affected:Humans and other mammals

Found: 160 nonactive | as graph: single | with analogs [1] << Back 151 152 153 154 155 156 157 158 159 160 Next >> [160]
Species: 4932
Condition: SWI4
Replicates: 2
Raw OD Value: r im 0.5472±0.00827315
Normalized OD Score: sc h 0.9577±0.014123
Z-Score: -1.9068±0.673339
p-Value: 0.0848478
Z-Factor: -1.95528
Fitness Defect: 2.4669
Bioactivity Statement: Nonactive
Experimental Conditions
Library:SPECMTS3
Plate Number and Position:20|A2
Drug Concentration:50.00 nM
OD Absorbance:600 nm
Robot Temperature:26.30 Celcius
Date:2008-02-07 YYYY-MM-DD
Plate CH Control (+):0.042175000000000004±0.00045
Plate DMSO Control (-):0.5722±0.01254
Plate Z-Factor:0.9079
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DBLink | Rows returned: 3
2578 1,3-bis(2-chloroethyl)-1-nitroso-urea
151563 1,3-bis(2-chloroethyl)-1-nitroso-urea
450682 1,3-bis(2-chloroethyl)-1-nitroso-urea

internal high similarity DBLink | Rows returned: 1
LOPAC 00744 1.0000

active | Cluster 2382 | Additional Members: 3 | Rows returned: 1
SPE01503422 0.565217391304348

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