WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 408014

CAS#: 2370952-98-8

Description: FAPI-2 is a Quinoline-Based Theranostic Ligands for the Targeting of Fibroblast Activation Protein. FAPI-2 is a ligand to make 68Ga-​FAPI-​2, which is a PET tracer that act as FAP inhibitor (FAPI). 68Ga-​FAPI-​2 demonstrated promising result. FAPI PET​/CT is a new diagnostic method in imaging cancer patients. In contrast to 18F-​FDG, no diet or fasting in prepn. for the examn. is necessary, and image acquisition can potentially be started a few minutes after tracer application. Tumor-​to-​background contrast ratios were equal to or even better than those of 18F-​FDG.

Chemical Structure

CAS# 2370952-98-8

Theoretical Analysis

MedKoo Cat#: 408014
Name: FAPI-2
CAS#: 2370952-98-8
Chemical Formula: C40H56N10O10
Exact Mass: 836.4181
Molecular Weight: 836.948
Elemental Analysis: C, 57.40; H, 6.74; N, 16.74; O, 19.12

Price and Availability

This product is not in stock, which may be available by custom synthesis. For cost-effective reason, minimum order is 1g (price is usually high, lead time is 2~3 months, depending on the technical challenge). Quote less than 1g will not be provided. To request quote, please email to sales @medkoo.com or click below button.
Note: Price will be listed if it is available in the future.

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Synonym: FAPI-02; FAPI02; FAPI 02; FAPI-2; FAPI2; FAPI 2;

IUPAC/Chemical Name: (S)-2,2',2''-(10-(2-(4-(3-((4-((2-(2-cyanopyrrolidin-1-yl)-2-oxoethyl)carbamoyl)quinolin-6-yl)oxy)propyl)piperazin-1-yl)-2-oxoethyl)-1,4,7,10-tetraazacyclododecane-1,4,7-triyl)triacetic acid


InChi Code: InChI=1S/C40H56N10O10/c41-24-30-3-1-9-50(30)35(51)25-43-40(59)32-6-7-42-34-5-4-31(23-33(32)34)60-22-2-8-44-18-20-49(21-19-44)36(52)26-45-10-12-46(27-37(53)54)14-16-48(29-39(57)58)17-15-47(13-11-45)28-38(55)56/h4-7,23,30H,1-3,8-22,25-29H2,(H,43,59)(H,53,54)(H,55,56)(H,57,58)/t30-/m0/s1


Appearance: Solid powder

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: 2934.99.9001

Preparing Stock Solutions

The following data is based on the product molecular weight 836.948 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.

Recalculate based on batch purity %
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

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1: Kratochwil C, Flechsig P, Lindner T, Abderrahim L, Altmann A, Mier W, Adeberg
S, Rathke H, Röhrich M, Winter H, Plinkert PK, Marme F, Lang M, Kauczor HU, Jäger
D, Debus J, Haberkorn U, Giesel FL. (68)Ga-FAPI PET/CT: Tracer Uptake in 28
Different Kinds of Cancer. J Nucl Med. 2019 Jun;60(6):801-805. doi:
10.2967/jnumed.119.227967. Epub 2019 Apr 6. PubMed PMID: 30954939.

2: Loktev A, Lindner T, Burger EM, Altmann A, Giesel F, Kratochwil C, Debus J,
Marme F, Jaeger D, Mier W, Haberkorn U. Development of novel FAP-targeted
radiotracers with improved tumor retention. J Nucl Med. 2019 Mar 8. pii:
jnumed.118.224469. doi: 10.2967/jnumed.118.224469. [Epub ahead of print] PubMed
PMID: 30850501.

3: Lindner T, Loktev A, Altmann A, Giesel F, Kratochwil C, Debus J, Jäger D, Mier
W, Haberkorn U. Development of Quinoline-Based Theranostic Ligands for the
Targeting of Fibroblast Activation Protein. J Nucl Med. 2018 Sep;59(9):1415-1422.
doi: 10.2967/jnumed.118.210443. Epub 2018 Apr 6. PubMed PMID: 29626119.

Additional Information

Fibroblast activation protein (FAP) is overexpressed in cancer-associated fibroblasts and is involved in a variety of tumor-promoting activities such as matrix remodeling, angiogenesis, chemotherapy resistance, and immunosuppression. Because FAP shows low expression in most normal organs, it presents an interesting target for imaging and endoradiotherapy.