Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T12452 |
Digeranyl bisphosphonate
DGBP |
Rho; Ras | Cell Cycle/Checkpoint; GPCR/G Protein; MAPK |
Digeranyl bisphosphonate (DGBP) 是一种有效的香叶基焦磷酸香叶酯 (GGPP) 合酶抑制剂,对 Rac1 的香叶基焦磷酸化有抑制作用。Digeranyl bisphosphonate 诱导细胞发生自噬却不诱导细胞凋亡。 | |||
T69443 |
Aminobutane bisphosphonate
|
||
Aminobutane bisphosphonate is a powerful inhibitor of bone resorption. It can potentially be a useful measure for controlling hypercalcemia in patients with carcinoma. | |||
T6739 |
Zoledronic Acid
CGP-4244,CGP42446A,唑来膦酸,Zoledronate,CGP 42446,ZOL 446,Zometa |
Apoptosis; Rho; Autophagy | Apoptosis; Autophagy; Cell Cycle/Checkpoint |
Zoledronic Acid (ZOL 446) 是一种含氮二磷酸盐,能抑制破骨细胞的分化和凋亡,具有高效的抗骨质再吸收活性,也有抗癌作用。 | |||
T21299 |
Zoledronic acid monohydrate
唑来膦酸一水合物,zoledronate,ZOL 446,CGP 42446,CGP42446A,Zoledronic acid hydrate |
Apoptosis; Others; Autophagy | Apoptosis; Autophagy; Others |
Zoledronic acid monohydrate (CGP 42446) 是一种含氮二磷酸盐,具有高效的抗骨质再吸收活性。它能抑制破骨细胞的分化和凋亡,有抗癌作用。 | |||
T1599 |
Ibandronic acid
Bonviva,Bondronat,Boniva,伊班膦酸 |
Others; HBV | Microbiology/Virology; Others |
Ibandronic acid (Bonviva) 是一种高效含氮双磷酸盐,可作用于骨质疏松,具有抗吸收和抗高钙血症作用。 | |||
T1337 |
Pamidronate Disodium
帕米膦酸钠,CGP 23339A,CGP 23339AE,Pamidronate disodium salt |
Others; HBV | Microbiology/Virology; Others |
Pamidronate Disodium (CGP 23339A) 是一种具有强化骨骼作用的物质。 | |||
T73506 |
TH-Z93
THZ93 |
Antibacterial | Microbiology/Virology |
TH-Z93 是一种有效的 FPPS 抑制剂 (IC50: 90 nM),也是一种亲脂性双膦酸盐。 | |||
T1599L |
Ibandronate sodium
伊班膦酸钠,Boniva,Ibandronate sodium salt,Bondronat |
HBV; Transferase | Metabolism; Microbiology/Virology |
Ibandronate sodium (Boniva) 是一种高活性的含氮二磷酸盐,可用于骨质疏松的研究。 | |||
T6539 |
Ibandronate sodium monohydrate
Boniva monohydrate,Bondronat monohydrate,Ibandronate sodium,伊班膦酸钠单水合物,BM-210955,BM-21.0955,伊班膦酸钠一水合物,RPR-102289A |
Apoptosis; Others | Apoptosis; Others |
Ibandronate sodium monohydrate (BM-210955) 是一种高活性的含氮二磷酸盐,可用于骨质疏松。 | |||
T6373 |
Alendronate sodium hydrate
G-704650,Alendronate,MK 217,Alendronate sodium trihydrate,阿仑膦酸钠,G-704650 Adronat,Fosamax |
Transferase | Metabolism |
Alendronate sodium hydrate (MK 217) 是 farnesyl diphosphate synthase 抑制剂(IC50:460 nM)。 | |||
T6451 |
Clodronic acid disodium salt
Loron,Clodronate Disodium,氯屈膦酸二钠,Lodronate |
Others | Others |
Clodronic acid disodium salt (Lodronate) 是一种口服具有活力的破骨细胞骨吸收 (osteoclastic bone resorption) 的抑制剂,是一代双磷酸盐。它可用于高骨转换状态、Paget’s 病和溶骨性骨转移中。 | |||
T16289 |
NE 10790
3-PEHPC |
Others | Others |
NE 10790 (3-PEHPC) 是一种二磷酸利塞磷酸盐的磷酸酯类似物,是一种法尼焦磷酸合成酶的弱抑制剂,也是一种弱抗吸收剂。 | |||
T19415 |
Medronic acid
亚甲基二磷酸,Methylenediphosphonic acid |
Others | Others |
Medronic acid (Methylenediphosphonic acid) 是一种亚甲基取代的二膦酸盐。它对骨基质中的羟基磷灰石晶体的表面具有亲和力,并且可粘附在其表面。它能够在类骨质矿化的位点累积,可以在骨成像中与放射性同位素复合使用。 | |||
T14766 |
BPH-715
|
Others; Parasite | Microbiology/Virology; Others |
BPH-715 抑制恶性疟原虫的肝脏阶段生长,对 HepG2 细胞中的恶性疟原虫外红细胞的形成的 IC50 为 10 μM。 | |||
T10586L |
BPH-1358
NSC50460 |
Others; Antibacterial | Microbiology/Virology; Others |
BPH-1358 (NSC-50460) 是一种人 FPPS 和 UPPS 抑制剂,IC50值分别为 1.8 μM 和 110 nM,对金黄色葡萄球菌的 MIC 值大约为 250 ng/mL。 | |||
T33873 |
Pamidronate monosodium
Pamidronic acid monosodium salt,J710.127I,Pamidronate-monosodium |
||
Pamidronate monosodium is a bisphosphonate. | |||
T26928 |
BV600022
BV-600022,BV 600022 |
||
BV600022 is an osteoadsorptive bisphosphonate-ciprofloxacin conjugate with antibacterial activity. | |||
T28151 |
NE21650
NE-21650,NE 21650 |
||
NE21650, a bisphosphonate, inhibits isopentenyl diphosphate isomerase and farnesyl diphosphate synthase. | |||
T30836 |
Cgp 47072
Cgp-47072,Cgp47072 |
||
Cgp 47072 is a bisphosphonate, used in the treatment of bone diseases, particularly where there is uncontrolled bone resorption. | |||
T11956L |
MBC-11
|
Others | Others |
MBC-11 is a first-in-class conjugate of the bone-targeting bisphosphonate etidronate covalently linked to the antimetabolite cytarabine (araC). It also has the potential to treat tumor-induced bone disease (TIBD). | |||
T61764 | Zoledronic acid disodium tetrahydrate | ||
Zoledronic Acid (Zoledronate) disodium tetrahydrate is a potent third-generation bisphosphonate (BP), exhibiting strong anti-resorptive activity. It effectively inhibits osteoclast differentiation and apoptosis, while also demonstrating anti-cancer properties [1]. | |||
T11956 |
MBC-11 triethylamine
|
Others | Others |
MBC-11 triethylamine has potential to treat tumor-induced bone disease (TIBD), is a first-in-class conjugate of the bone-targeting bisphosphonate etidronate covalently linked to the antimetabolite cytarabine (araC). | |||
T11957 | MBC-11 trisodium | Others | Others |
MBC-11 trisodium has potential to treat tumor-induced bone disease (TIBD).It is a first-in-class conjugate of the bone-targeting bisphosphonate HEDP covalently linked to the antimetabolite Ara-C. | |||
T39037 |
Tiludronate disodium hemihydrate
Tiludronic acid disodium hemihydrate,替鲁膦酸二钠半水合物 |
||
Tiludronate (Tiludronic Acid) disodium hemihydrate is an orally active bisphosphonate compound that functions as an osteoregulator. It is primarily utilized in metabolic bone disorder research. This compound acts as a potent inhibitor of the osteoclast vacuolar H+ -ATPase and possesses antiresorptive and anti-inflammatory properties[4]. | |||
T73056 |
Tiludronate
Tiludronic acid |
||
Tiludronate (Tiludronic Acid) 是一种口服活性双膦酸盐,可以起到骨调节作用。Tiludronate 用于代谢性骨疾病的研究。Tiludronate 是破骨细胞空泡 H(+)-ATP 酶的有效抑制剂。 | |||
T72989 |
hGGPPS-IN-3
|
Apoptosis | Apoptosis |
hGGPPS-IN-3(Compound 13h)是一种针对人类香叶基香叶基焦磷酸合成酶(hGGPPS)的有效抑制剂,属于C-2取代的噻吩并嘧啶基双膦酸盐(C2-ThP-BPs)衍生物。该化合物能够诱导多发性骨髓瘤(MM)细胞具有选择性地进入凋亡(apoptosis),并且在体内展现了对抗骨髓瘤的活性。 | |||
T70045 | HUN47990 | ||
HUN47990 is a bisphosphonate (BP) prodrug with antitumor activity. HUN47990 potently inhibits the in vitro growth of a variety of tumor cell lines, especially hematopoietic cell lines, at nanomolar concentrations. HUN47990 inhibited the prenylation of the RAP1A small GTPase signaling protein at concentrations as low as 1-10 nM. HUN47990 slowed the growth of human bladder cancer cells in an immunodeficient mouse model. HUN47990 is significantly more active than zoledronic acid, the most active FD... | |||
T10586 |
BPH-1358 free base
NSC50460 free base |
Others | Others |
BPH-1358 (NSC50460) free base is a potent human undecaprenyl diphosphate synthase (UPPS) and farnesyl diphosphate synthase (FPPS) inhibitor (IC50s: 110 nM and 1.8 μM) and is active against S. aureus in vitro (MIC ~250 ng/mL). |