Synonym
Neothramycin A; Antibiotic MC-916-A; MC-916-A
IUPAC/Chemical Name
5H-Pyrrolo(2,1-c)(1,4)benzodiazepin-5-one, 1,2,3,11a-tetrahydro-3,8-dihydroxy-7-methoxy-, (3S-trans)-
InChi Key
FXMOIYLVKOALHC-MADCSZMMSA-N
InChi Code
InChI=1S/C13H14N2O4/c1-19-11-4-8-9(5-10(11)16)14-6-7-2-3-12(17)15(7)13(8)18/h4-7,12,16-17H,2-3H2,1H3/t7-,12-/m0/s1
SMILES Code
O=C1N2[C@](CC[C@@H]2O)([H])C=NC3=CC(O)=C(OC)C=C13
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.03.00
Preparing Stock Solutions
The following data is based on the
product
molecular weight
262.27
Batch specific molecular weights may vary
from batch to batch
due to the degree of hydration, which will
affect the solvent
volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass |
1 mg |
5 mg |
10 mg |
1 mM |
1.15 mL |
5.76 mL |
11.51 mL |
5 mM |
0.23 mL |
1.15 mL |
2.3 mL |
10 mM |
0.12 mL |
0.58 mL |
1.15 mL |
50 mM |
0.02 mL |
0.12 mL |
0.23 mL |
1: Rao SN, Remers WA. All atom molecular mechanics simulations on covalent complexes of anthramycin and neothramycin with deoxydecanucleotides. J Med Chem. 1990 Jun;33(6):1701-7. PubMed PMID: 2342065.
2: Remers WA, Mabilia M, Hopfinger AJ. Conformations of complexes between pyrrolo[1,4]benzodiazepines and DNA segments. J Med Chem. 1986 Dec;29(12):2492-503. PubMed PMID: 3783609.
3: Petrusek RL, Anderson GL, Garner TF, Fannin QL, Kaplan DJ, Zimmer SG, Hurley LH. Pyrrol[1,4]benzodiazepine antibiotics. Proposed structures and characteristics of the in vitro deoxyribonucleic acid adducts of anthramycin, tomaymycin, sibiromycin, and neothramycins A and B. Biochemistry. 1981 Mar 3;20(5):1111-9. PubMed PMID: 6261786.
4: Morris SJ, Thurston DE, Nevell TG. Evaluation of the electrophilicity of DNA-binding pyrrolo[2,1-c][1,4]benzodiazepines by HPLC. J Antibiot (Tokyo). 1990 Oct;43(10):1286-92. PubMed PMID: 2258327.