In vivo
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DM1-SMCC

In vivo
Product Name
DM1-SMCC
CAS No.
1228105-51-8
Chemical Name
DM1-SMCC
Synonyms
DM1-SMC;SMCC-DM1;SMCC-MDC;DM1-SMCC;DMI-SMCC;DMA-SMCC;DM1 SMCC; DM1SMCC;SMCC-DM1 (DM1-SMCC);Phenol,4-chloro-4-iodo-;High quality 1228105-51-8 DM1-SMCC
CBNumber
CB62730877
Molecular Formula
C51H66ClN5O16S
Formula Weight
1072.61
MOL File
1228105-51-8.mol
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DM1-SMCC Property

Melting point:
>166°C (dec.)
Density 
1.41±0.1 g/cm3(Predicted)
storage temp. 
-20°C Freezer
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
9.82±0.70(Predicted)
form 
Solid
color 
White to Off-White
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Cayman Chemical
Product number
23926
Product name
DM1-SMCC
Purity
≥98%
Packaging
1mg
Price
$93
Updated
2024/03/01
Cayman Chemical
Product number
23926
Product name
DM1-SMCC
Purity
≥98%
Packaging
5mg
Price
$230
Updated
2024/03/01
Cayman Chemical
Product number
23926
Product name
DM1-SMCC
Purity
≥98%
Packaging
10mg
Price
$412
Updated
2024/03/01
Cayman Chemical
Product number
23926
Product name
DM1-SMCC
Purity
≥98%
Packaging
25mg
Price
$911
Updated
2024/03/01
Usbiological
Product number
466180
Product name
SMCC-DM1
Packaging
1mg
Price
$368
Updated
2021/12/16
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DM1-SMCC Chemical Properties,Usage,Production

In vivo

The antitumor effect of murine/human chimeric CD138-specific monoclonal antibody nBT062 conjugated with highly cytotoxic maytansinoid derivatives against multiple myeloma (MM) cells were investigated in vitro and in vivo. The in vivo activity of BT062SPDB-DM4, BT062-SMCC-DM1, and BT062-SPP-DM was examined in murine MM cell xenograft model of human and severe combined immunodeficient (SCID) mice bearing implant bone chips injected with human MM cells (SCID-hu model). The in vivo efficacy of nBT062-SPDB-DM4, nBT062-SMCC-DM1, and nBT062-SPP-DM1 was next evaluated in SCID mice bearing established CD138-positive MOLP-8 human MM cells. A single i.v. administration of the immunoconjugates caused significant dose-dependent tumor growth inhibition and tumor regression at concentrations that were well tolerated, evidenced by stable body weight. nBT062SPDB-DM4 was the most active conjugate tested in this model (Fig. 6A ). In addition, weekly dosing of the nBT062-SMCC-DM1 (six doses of 13.8 μg/kg) completely blocked tumor growth during the dosing period (Supplementary Fig. S6A). In summary, nBT062-SMCC-DM1, nBT062-SPDB-DM4, and nBT062-SPP-DM1 have in vitro and in vivo antitumor activity against CD138positive MM cells and can overcome the protective effects of cytokines and BMSCs Clin Cancer Res. 2009 Jun 15;15(12):4028-37. https://pubmed.ncbi.nlm.nih.gov/19509164/

Description

DM1-SMCC is a drug-linker conjugate composed of a potent microtubule-disrupting agent DM1 and a linker SMCC.

Uses

SMCC-DM1 is a mertansine drug (DM1) with a reactive linker SMCC to make antibody drug conjugate. DM1 (mertansine), a thiol-containing maytansinoid, is a potent microtubule-disrupting agent.

in vitro

In particular, the metabolic fate in cells of huC242-maytansinoid conjugates containing either a disulfide linker (huC242-SPDB-DM4) or a thioether linker (huC242-SMCC-DM1) was examined. The disulfide-linked antibody-maytansinoid conjugate, huC242-SPDBDM4, and the thioether-linked conjugate, huC242-SMCC-DM1, were first assayed for their cytotoxic potency against antigen-positive COLO 205 cells and antigen-negative Namalwa cells (both sensitive to maytansine with IC50 values of ~30 to 60 pmol/L for both cell lines) using an 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT)–based assay. The conjugates displayed similar potencies with IC50 values of 40 pmol/L against COLO 205 cells and 20 to 80 nmol/L against Namalwa cells upon a 4-day exposure of the cells to the conjugates ( Fig. 1A ). To examine the fate of the maytansinoid drug upon incubation of target cells with an antibody-maytansinoid conjugate, conjugates with maytansinoids were prepared that were 3H-labeled at the C-20 methoxy group (see Fig. 5). Radiolabeled maytansinoid conjugates, huC242-SPDB-[3H]DM4 (250 mCi/mmol) and huC242-SMCC-[3H]DM1 (214 mCi/mmol), exhibit in vitro cytotoxicities similar to nonradiolabeled conjugate samples (data not shown). The two major metabolites, S-methyl-DM4 and lysine-Nε-SMCC-DM1, were synthesized and tested for their in vitro cytotoxicity against COLO 205 cells and Namalwa cells. Lysine-Nε-SMCC-DM1 was ~105-fold less potent against both cell lines with an IC50 value of 0.1 μmol/L (data not shown). Accumulation of the lysine-Nε-SMCC-DM1 metabolite from the noncleavable conjugate is coincident with the observed formation of the potent S-methyl-DM4, DM4, and lysine-Nε-SPDB-DM4 from the cleavable conjugate. This suggests that the lysineNε-SMCC-DM1 metabolite is as potent as the metabolites from the cleavable conjugate when delivered intracellularly and that all of the maytansinoid metabolites are active when produced in the cell. Cancer Res. 2006 Apr 15;66(8):4426-33. https://pubmed.ncbi.nlm.nih.gov/16618769/

DM1-SMCC Preparation Products And Raw materials

Raw materials

Preparation Products

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DM1-SMCC Suppliers

Levena (Suzhou) Biopharma Co., Ltd.
Tel
0512-81877925 051281877925
Email
info@levena.cn
Country
China
ProdList
48
Advantage
58
Zhejiang Huida Biotech Co., LTD
Tel
0571-89903882 13626641628
Email
jiangnan@huidabiotech.com
Country
China
ProdList
3661
Advantage
58
Chembest Research Laboratories Limited
Tel
021-20908456
Fax
021-58180499
Email
sales@BioChemBest.com
Country
China
ProdList
6011
Advantage
61
T&W GROUP
Tel
021-61551611 13296011611
Fax
+86 21-50676805
Email
contact@trustwe.com
Country
China
ProdList
9900
Advantage
58
Shanghai Topbiochem Technology Co., Ltd
Tel
021-58170097
Email
info@topbiochem.com
Country
China
ProdList
9452
Advantage
58
MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4863
Advantage
58
TargetMol Chemicals Inc.
Tel
021-33632979 15002134094
Fax
021-33632979
Email
marketing@targetmol.com
Country
China
ProdList
7934
Advantage
58
BrightGene Bio-medical Technology Co., Ltd.
Tel
0512-0512-62551764 18013103761
Fax
0512-62551799
Email
sales01@bright-gene.com
Country
China
ProdList
61
Advantage
70
Shandong Juntai Pharmaceutical Co., LTD.
Tel
18963498209
Fax
0531-66958526
Email
sales@h2opharm.com
Country
China
ProdList
134
Advantage
55
AdooQ Bioscience CHINA
Tel
025-58849295 18951903616;
Fax
025-68650336
Email
info@adooq.cn
Country
China
ProdList
2989
Advantage
60
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View Lastest Price from DM1-SMCC manufacturers

Henan Fengda Chemical Co., Ltd
Product
DM1-SMCC 1228105-51-8
Price
US $50.00-1.00/KG
Min. Order
1KG
Purity
99%
Supply Ability
g-kg-tons, free sample is available
Release date
2023-12-22

1228105-51-8, DM1-SMCCRelated Search:


  • DM1-SMCC
  • N2'-Deacetyl-N2'-[3-[[1-[[4-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]cyclohexyl]methyl]-2,5-dioxo-3-pyrrolidinyl]thio]-1-oxopropyl]-maytansine
  • SMCC-DM1
  • DM1-SMC
  • SMCC-DM1 (DM1-SMCC)
  • SMCC-MDC
  • Maytansine, N2'-deacetyl-N2'-[3-[[1-[[4-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]cyclohexyl]methyl]-2,5-dioxo-3-pyrrolidinyl]thio]-1-oxopropyl]-
  • DM1 SMCC; DM1SMCC
  • DMI-SMCC
  • N<sup>2'</sup>-deacetyl-N<sup>2'</sup>-[3-[[1-[[4-[[(2,5-dioxo-1-pyrrolidinyl)oxy]carbonyl]cyclohexyl]methyl]-2,5-dioxo-3-pyrrolidinyl]thio]-1-oxopropyl]-maytansine
  • 2,5-Dioxopyrrolidin-1-yl 4-((3-((3-(((2S)-1-(((14S,16S,33S,2R,4R,10E,12Z,14R)-86-chloro-14-hydroxy-85,14-dimethoxy-33,2,7,10-tetramethyl-12,6-dioxo-7-aza-1(6,4)-oxazinana-3(2,3)-oxirana-8(1,3)-benzenacyclotetradecaphane-10,12-dien-4-yl)oxy)-1-oxopropan-2-yl)(methyl)amino)-3-oxopropyl)thio)-2,5-dioxopyrrolidin-1-yl)methyl)cyclohexane-1-carboxylate
  • Phenol,4-chloro-4-iodo-
  • High quality 1228105-51-8 DM1-SMCC
  • DMA-SMCC
  • 1228105-51-8
  • C51H66ClN5O16S
  • Pharmaceutical