IMC-1C11

DB06101

biotech investigational

Deskripsi

IMC-1C11 is an anti-angiogenesis agent. It is a chimeric anti-kinase insert domain-containing receptor (KDR) antibody that blocks VEGFR-KDR interaction and inhibits VEGFR-induced endothelial cell proliferation. IMC-1C11 is used for treatment of patients with liver metastases from colorectal carcinoma.

Struktur Molekul 2D

Struktur tidak tersedia

Peta Jejaring Molekuler
Legenda: ObatTargetGenEnzim(Panah → menunjukkan arah efek / relasi)TransporterCarrier

Profil Farmakokinetik

Waktu Paruh (Half-Life) -
Volume Distribusi -
Klirens (Clearance) -

Absorpsi

Data absorpsi tidak tersedia.

Metabolisme

Data metabolisme tidak tersedia.

Rute Eliminasi

Data eliminasi belum tersedia.

Interaksi Obat

372 Data
Diethylstilbestrol Diethylstilbestrol may increase the thrombogenic activities of IMC-1C11.
Chlorotrianisene Chlorotrianisene may increase the thrombogenic activities of IMC-1C11.
Conjugated estrogens Conjugated estrogens may increase the thrombogenic activities of IMC-1C11.
Estrone Estrone may increase the thrombogenic activities of IMC-1C11.
Estradiol Estradiol may increase the thrombogenic activities of IMC-1C11.
Dienestrol Dienestrol may increase the thrombogenic activities of IMC-1C11.
Ethinylestradiol Ethinylestradiol may increase the thrombogenic activities of IMC-1C11.
Mestranol Mestranol may increase the thrombogenic activities of IMC-1C11.
Estriol Estriol may increase the thrombogenic activities of IMC-1C11.
Estrone sulfate Estrone sulfate may increase the thrombogenic activities of IMC-1C11.
Quinestrol Quinestrol may increase the thrombogenic activities of IMC-1C11.
Hexestrol Hexestrol may increase the thrombogenic activities of IMC-1C11.
Tibolone Tibolone may increase the thrombogenic activities of IMC-1C11.
Synthetic Conjugated Estrogens, A Synthetic Conjugated Estrogens, A may increase the thrombogenic activities of IMC-1C11.
Synthetic Conjugated Estrogens, B Synthetic Conjugated Estrogens, B may increase the thrombogenic activities of IMC-1C11.
Polyestradiol phosphate Polyestradiol phosphate may increase the thrombogenic activities of IMC-1C11.
Esterified estrogens Esterified estrogens may increase the thrombogenic activities of IMC-1C11.
Zeranol Zeranol may increase the thrombogenic activities of IMC-1C11.
Equol Equol may increase the thrombogenic activities of IMC-1C11.
Promestriene Promestriene may increase the thrombogenic activities of IMC-1C11.
Methallenestril Methallenestril may increase the thrombogenic activities of IMC-1C11.
Epimestrol Epimestrol may increase the thrombogenic activities of IMC-1C11.
Moxestrol Moxestrol may increase the thrombogenic activities of IMC-1C11.
Estradiol acetate Estradiol acetate may increase the thrombogenic activities of IMC-1C11.
Estradiol benzoate Estradiol benzoate may increase the thrombogenic activities of IMC-1C11.
Estradiol cypionate Estradiol cypionate may increase the thrombogenic activities of IMC-1C11.
Estradiol valerate Estradiol valerate may increase the thrombogenic activities of IMC-1C11.
Biochanin A Biochanin A may increase the thrombogenic activities of IMC-1C11.
Formononetin Formononetin may increase the thrombogenic activities of IMC-1C11.
Estetrol Estetrol may increase the thrombogenic activities of IMC-1C11.
Cetuximab The risk or severity of adverse effects can be increased when Cetuximab is combined with IMC-1C11.
Human immunoglobulin G The risk or severity of adverse effects can be increased when Human immunoglobulin G is combined with IMC-1C11.
Omalizumab The risk or severity of adverse effects can be increased when Omalizumab is combined with IMC-1C11.
Adalimumab The risk or severity of adverse effects can be increased when Adalimumab is combined with IMC-1C11.
Abciximab The risk or severity of adverse effects can be increased when Abciximab is combined with IMC-1C11.
Gemtuzumab ozogamicin The risk or severity of adverse effects can be increased when Gemtuzumab ozogamicin is combined with IMC-1C11.
Indium In-111 satumomab pendetide The risk or severity of adverse effects can be increased when Indium In-111 satumomab pendetide is combined with IMC-1C11.
Infliximab The risk or severity of adverse effects can be increased when Infliximab is combined with IMC-1C11.
Trastuzumab The risk or severity of adverse effects can be increased when Trastuzumab is combined with IMC-1C11.
Rituximab The risk or severity of adverse effects can be increased when Rituximab is combined with IMC-1C11.
Basiliximab The risk or severity of adverse effects can be increased when Basiliximab is combined with IMC-1C11.
Muromonab The risk or severity of adverse effects can be increased when Muromonab is combined with IMC-1C11.
Digoxin Immune Fab (Ovine) The risk or severity of adverse effects can be increased when Digoxin Immune Fab (Ovine) is combined with IMC-1C11.
Ibritumomab tiuxetan The risk or severity of adverse effects can be increased when Ibritumomab tiuxetan is combined with IMC-1C11.
Tositumomab The risk or severity of adverse effects can be increased when Tositumomab is combined with IMC-1C11.
Alemtuzumab The risk or severity of adverse effects can be increased when Alemtuzumab is combined with IMC-1C11.
Capromab pendetide The risk or severity of adverse effects can be increased when Capromab pendetide is combined with IMC-1C11.
Efalizumab The risk or severity of adverse effects can be increased when Efalizumab is combined with IMC-1C11.
Antithymocyte immunoglobulin (rabbit) The risk or severity of adverse effects can be increased when Antithymocyte immunoglobulin (rabbit) is combined with IMC-1C11.
Natalizumab The risk or severity of adverse effects can be increased when Natalizumab is combined with IMC-1C11.
Palivizumab The risk or severity of adverse effects can be increased when Palivizumab is combined with IMC-1C11.
Daclizumab The risk or severity of adverse effects can be increased when Daclizumab is combined with IMC-1C11.
Bevacizumab The risk or severity of adverse effects can be increased when Bevacizumab is combined with IMC-1C11.
Technetium Tc-99m arcitumomab The risk or severity of adverse effects can be increased when Technetium Tc-99m arcitumomab is combined with IMC-1C11.
Eculizumab The risk or severity of adverse effects can be increased when Eculizumab is combined with IMC-1C11.
Panitumumab The risk or severity of adverse effects can be increased when Panitumumab is combined with IMC-1C11.
Ranibizumab The risk or severity of adverse effects can be increased when Ranibizumab is combined with IMC-1C11.
Galiximab The risk or severity of adverse effects can be increased when Galiximab is combined with IMC-1C11.
Pexelizumab The risk or severity of adverse effects can be increased when Pexelizumab is combined with IMC-1C11.
Afelimomab The risk or severity of adverse effects can be increased when Afelimomab is combined with IMC-1C11.
Epratuzumab The risk or severity of adverse effects can be increased when Epratuzumab is combined with IMC-1C11.
Bectumomab The risk or severity of adverse effects can be increased when Bectumomab is combined with IMC-1C11.
Oregovomab The risk or severity of adverse effects can be increased when Oregovomab is combined with IMC-1C11.
IGN311 The risk or severity of adverse effects can be increased when IGN311 is combined with IMC-1C11.
Adecatumumab The risk or severity of adverse effects can be increased when Adecatumumab is combined with IMC-1C11.
Labetuzumab The risk or severity of adverse effects can be increased when Labetuzumab is combined with IMC-1C11.
Matuzumab The risk or severity of adverse effects can be increased when Matuzumab is combined with IMC-1C11.
Fontolizumab The risk or severity of adverse effects can be increased when Fontolizumab is combined with IMC-1C11.
Bavituximab The risk or severity of adverse effects can be increased when Bavituximab is combined with IMC-1C11.
CR002 The risk or severity of adverse effects can be increased when CR002 is combined with IMC-1C11.
Rozrolimupab The risk or severity of adverse effects can be increased when Rozrolimupab is combined with IMC-1C11.
Girentuximab The risk or severity of adverse effects can be increased when Girentuximab is combined with IMC-1C11.
Obiltoxaximab The risk or severity of adverse effects can be increased when Obiltoxaximab is combined with IMC-1C11.
XTL-001 The risk or severity of adverse effects can be increased when XTL-001 is combined with IMC-1C11.
NAV 1800 The risk or severity of adverse effects can be increased when NAV 1800 is combined with IMC-1C11.
Briakinumab The risk or severity of adverse effects can be increased when Briakinumab is combined with IMC-1C11.
Otelixizumab The risk or severity of adverse effects can be increased when Otelixizumab is combined with IMC-1C11.
AMG 108 The risk or severity of adverse effects can be increased when AMG 108 is combined with IMC-1C11.
Iratumumab The risk or severity of adverse effects can be increased when Iratumumab is combined with IMC-1C11.
Enokizumab The risk or severity of adverse effects can be increased when Enokizumab is combined with IMC-1C11.
Ramucirumab The risk or severity of adverse effects can be increased when Ramucirumab is combined with IMC-1C11.
Farletuzumab The risk or severity of adverse effects can be increased when Farletuzumab is combined with IMC-1C11.
Veltuzumab The risk or severity of adverse effects can be increased when Veltuzumab is combined with IMC-1C11.
Ustekinumab The risk or severity of adverse effects can be increased when Ustekinumab is combined with IMC-1C11.
Trastuzumab emtansine The risk or severity of adverse effects can be increased when Trastuzumab emtansine is combined with IMC-1C11.
PRO-542 The risk or severity of adverse effects can be increased when PRO-542 is combined with IMC-1C11.
TNX-901 The risk or severity of adverse effects can be increased when TNX-901 is combined with IMC-1C11.
Inotuzumab ozogamicin The risk or severity of adverse effects can be increased when Inotuzumab ozogamicin is combined with IMC-1C11.
RI 624 The risk or severity of adverse effects can be increased when RI 624 is combined with IMC-1C11.
Stamulumab The risk or severity of adverse effects can be increased when MYO-029 is combined with IMC-1C11.
CT-011 The risk or severity of adverse effects can be increased when CT-011 is combined with IMC-1C11.
Leronlimab The risk or severity of adverse effects can be increased when Leronlimab is combined with IMC-1C11.
Glembatumumab vedotin The risk or severity of adverse effects can be increased when Glembatumumab vedotin is combined with IMC-1C11.
Olaratumab The risk or severity of adverse effects can be increased when Olaratumab is combined with IMC-1C11.
IPH 2101 The risk or severity of adverse effects can be increased when IPH 2101 is combined with IMC-1C11.
TB-402 The risk or severity of adverse effects can be increased when TB-402 is combined with IMC-1C11.
Caplacizumab The risk or severity of adverse effects can be increased when Caplacizumab is combined with IMC-1C11.
Eldelumab The risk or severity of adverse effects can be increased when IMC-1C11 is combined with Eldelumab.
Lumiliximab The risk or severity of adverse effects can be increased when IMC-1C11 is combined with Lumiliximab.
Canakinumab The risk or severity of adverse effects can be increased when IMC-1C11 is combined with Canakinumab.

Target Protein

Vascular endothelial growth factor receptor 1 FLT1
Vascular endothelial growth factor receptor 2 KDR
Vascular endothelial growth factor receptor 3 FLT4

Referensi & Sumber

Artikel (PubMed)
  • PMID: 12684400
    Posey JA, Ng TC, Yang B, Khazaeli MB, Carpenter MD, Fox F, Needle M, Waksal H, LoBuglio AF: A phase I study of anti-kinase insert domain-containing receptor antibody, IMC-1C11, in patients with liver metastases from colorectal carcinoma. Clin Cancer Res. 2003 Apr;9(4):1323-32.
  • PMID: 17851838
    Lam T, Hetherington JW, Greenman J, Little S, Maraveyas A: Metronomic chemotherapy dosing-schedules with estramustine and temozolomide act synergistically with anti-VEGFR-2 antibody to cause inhibition of human umbilical venous endothelial cell growth. Acta Oncol. 2007;46(8):1169-77.
  • PMID: 15238424
    Wang ES, Teruya-Feldstein J, Wu Y, Zhu Z, Hicklin DJ, Moore MA: Targeting autocrine and paracrine VEGF receptor pathways inhibits human lymphoma xenografts in vivo. Blood. 2004 Nov 1;104(9):2893-902. Epub 2004 Jul 6.

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Sekuens Gen/Protein (FASTA)

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